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Cochrane Database of Systematic Reviews

Tratamiento de la pulpa para el deterioro extenso de los dientes primarios

Información

DOI:
https://doi.org/10.1002/14651858.CD003220.pub3Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 31 mayo 2018see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Salud oral

Copyright:
  1. Copyright © 2018 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Autores

  • Violaine Smaïl‐Faugeron

    Correspondencia a: Department of Dental Materials (Urb2i, EA4462), Université Paris Descartes ‐ Sorbonne Paris Cité, Montrouge, France

    [email protected]

  • Anne‐Marie Glenny

    Division of Dentistry, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK

  • Frédéric Courson

    Department of Dental Materials (Urb2i, EA4462), Université Paris Descartes ‐ Sorbonne Paris Cité, Montrouge, France

  • Pierre Durieux

    Department of Public Health and Medical Informatics, Georges Pompidou European Hospital, Paris, France

  • Michele Muller‐Bolla

    Department of Pediatric Dentistry, UFR Odontology, University of the Côte d’Azur, Nice, France

  • Helene Fron Chabouis

    Department of Dental Materials (Urb2i, EA4462), Université Paris Descartes ‐ Sorbonne Paris Cité, Montrouge, France

Contributions of authors

Conceiving the review ‐ Violaine Smaïl‐Faugeron (VSF), Hélène Fron Chabouis (HFC), Michele Muller‐Bolla (MMB), Anne‐Marie Glenny (AMG)
Designing the review ‐ VSF, HFC, Pierre Durieux (PD), Frédéric Courson (FC), AMG
Co‐ordinating the review ‐ VSF, HFC
Developing the search strategy ‐ VSF, HFC, AMG, Anne Littlewood (AL)
Undertaking searches ‐ VSF, HFC, AL
Screening search results ‐ VSF, HFC
Organising the retrieval of papers ‐ VSF
Screening the retrieved papers against inclusion criteria ‐ VSF, HFC
Appraising the quality of papers ‐ VSF, HFC
Extracting data from papers ‐ VSF, HFC
Writing to authors of papers for additional information ‐ VSF, HFC
Data management for the review ‐ VSF
Entering data into RevMan ‐ VSF
Analysis of data ‐ VSF
Interpretation of data ‐ VSF, HFC, FC
Writing the review ‐ VSF, HFC, PD, FC

Sources of support

Internal sources

  • School of Dentistry, The University of Manchester, Manchester Academic Health Sciences Centre (MAHSC), the NIHR Manchester Biomedical Research Centre, UK.

  • School of Dentistry, The University of Manchester, UK.

External sources

  • Cochrane Oral Health Group Global Alliance, Other.

    The production of Cochrane Oral Health reviews has been supported financially by our Global Alliance since 2011 (oralhealth.cochrane.org/partnerships‐alliances). Contributors over the past year have been the American Association of Public Health Dentistry, USA; AS‐Akademie, Germany; the British Association for the Study of Community Dentistry, UK; the British Society of Paediatric Dentistry, UK; the Canadian Dental Hygienists Association, Canada; the Centre for Dental Education and Research at All India Institute of Medical Sciences, India; the National Center for Dental Hygiene Research & Practice, USA; New York University College of Dentistry, USA; NHS Education for Scotland, UK; and the Swiss Society for Endodontology, Switzerland.

  • National Institute for Health Research (NIHR), UK.

    This project was supported by the NIHR, via Cochrane Infrastructure funding to Cochrane Oral Health. The views and opinions expressed herein are those of the review authors and do not necessarily reflect those of the Systematic Reviews Programme, the NIHR, the NHS or the Department of Health.

Declarations of interest

Violaine Smaïl‐Faugeron: none known
Anne‐Marie Glenny: none known. I am Deputy Co‐ordinating Editor with Cochrane Oral Health.
Frédéric Courson: none known
Pierre Durieux: has received in the past three years research grants from the French Ministry of Health (PREQHOS, PHRC). He has been member of scientific committees of ANR (Agence Nationale de la Recherche), PREQHOS (Projets de Recherche en qualité hospitalière) and PREPS (Projets de Recherche en Performance de Soins) of the French Ministry of Health. He has received consultancies from Amgen and ONYX, and the Haute Autorité de Santé (HAS). The author has no financial relationships with any organisations that might have an interest in the review in the previous three years (except the fact that the author is employee of an acute care hospital).
Michele Muller‐Bolla: none known
Hélène Fron Chabouis: our lab (URB2i, Universite Paris Descartes) has developed industrial partnerships but these did not have any link with this review and did not influence my work.

Acknowledgements

For this update, we thank Helen Worthington, Laura MacDonald, Anne Littlewood and Philip Riley of Cochrane Oral Health. We also thank the referees Suzanne Dunkley and Jaap Veerkamp, and copy editor Ann Jones.

For previous versions of the review, we thank Anne Littlewood (Cochrane Oral Health) for design and conduct of search strategies; Luisa Fernandez Mauleffinch and Philip Riley (Cochrane Oral Health) for their assistance; Laura Smales (BioMedEditing, Toronto, Canada) for editing the manuscript; and Gill Nadin for contribution as an author.

Version history

Published

Title

Stage

Authors

Version

2018 May 31

Pulp treatment for extensive decay in primary teeth

Review

Violaine Smaïl‐Faugeron, Anne‐Marie Glenny, Frédéric Courson, Pierre Durieux, Michele Muller‐Bolla, Helene Fron Chabouis

https://doi.org/10.1002/14651858.CD003220.pub3

2014 Aug 06

Pulp treatment for extensive decay in primary teeth

Review

Violaine Smaïl‐Faugeron, Frédéric Courson, Pierre Durieux, Michele Muller‐Bolla, Anne‐Marie Glenny, Helene Fron Chabouis

https://doi.org/10.1002/14651858.CD003220.pub2

2003 Jan 20

Pulp treatment for extensive decay in primary teeth

Review

Gill Nadin, Beena Rani Goel, Albert Yeung, Anne‐Marie Glenny

https://doi.org/10.1002/14651858.CD003220

Differences between protocol and review

None.

Keywords

MeSH

PICO

Population
Intervention
Comparison
Outcome

El uso y la enseñanza del modelo PICO están muy extendidos en el ámbito de la atención sanitaria basada en la evidencia para formular preguntas y estrategias de búsqueda y para caracterizar estudios o metanálisis clínicos. PICO son las siglas en inglés de cuatro posibles componentes de una pregunta de investigación: paciente, población o problema; intervención; comparación; desenlace (outcome).

Para saber más sobre el uso del modelo PICO, puede consultar el Manual Cochrane.

Study flow diagram
Figuras y tablas -
Figure 1

Study flow diagram

Risk of bias summary: review authors' judgements about each risk of bias item for each included study
Figuras y tablas -
Figure 2

Risk of bias summary: review authors' judgements about each risk of bias item for each included study

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 1.1

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 1 Clinical failure.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 1.2

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 2 Radiological failure.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 3 Overall failure.
Figuras y tablas -
Analysis 1.3

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 3 Overall failure.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 4 Pain.
Figuras y tablas -
Analysis 1.4

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 4 Pain.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 5 Soft tissue pathology.
Figuras y tablas -
Analysis 1.5

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 5 Soft tissue pathology.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 6 Pathological mobility.
Figuras y tablas -
Analysis 1.6

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 6 Pathological mobility.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 7 Pathological radiolucency.
Figuras y tablas -
Analysis 1.7

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 7 Pathological radiolucency.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 8 Pathological root resorption.
Figuras y tablas -
Analysis 1.8

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 8 Pathological root resorption.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 9 Pulp canal obliteration.
Figuras y tablas -
Analysis 1.9

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 9 Pulp canal obliteration.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 10 Dentin bridge formation.
Figuras y tablas -
Analysis 1.10

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 10 Dentin bridge formation.

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 11 Physiological root resorption.
Figuras y tablas -
Analysis 1.11

Comparison 1 Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy, Outcome 11 Physiological root resorption.

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 2.1

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 1 Clinical failure.

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 2.2

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 2 Radiological failure.

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 2.3

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 3 Pain.

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 4 Soft tissue pathology.
Figuras y tablas -
Analysis 2.4

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 4 Soft tissue pathology.

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 5 Pathological radiolucency.
Figuras y tablas -
Analysis 2.5

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 5 Pathological radiolucency.

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 6 Pathological root resorption.
Figuras y tablas -
Analysis 2.6

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 6 Pathological root resorption.

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 7 Pulp canal obliteration.
Figuras y tablas -
Analysis 2.7

Comparison 2 Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy, Outcome 7 Pulp canal obliteration.

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 3.1

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 1 Clinical failure.

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 3.2

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 2 Radiological failure.

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 3.3

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 3 Pain.

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 4 Soft tissue pathology.
Figuras y tablas -
Analysis 3.4

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 4 Soft tissue pathology.

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 5 Pathological mobility.
Figuras y tablas -
Analysis 3.5

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 5 Pathological mobility.

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 6 Pathological radiolucency.
Figuras y tablas -
Analysis 3.6

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 6 Pathological radiolucency.

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 7 Pathological root resorption.
Figuras y tablas -
Analysis 3.7

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 7 Pathological root resorption.

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 8 Pulp canal obliteration.
Figuras y tablas -
Analysis 3.8

Comparison 3 Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 8 Pulp canal obliteration.

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 4.1

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 1 Clinical failure.

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 4.2

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 2 Radiological failure.

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 3 Overall failure.
Figuras y tablas -
Analysis 4.3

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 3 Overall failure.

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 4 Pain.
Figuras y tablas -
Analysis 4.4

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 4 Pain.

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 5 Soft tissue pathology.
Figuras y tablas -
Analysis 4.5

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 5 Soft tissue pathology.

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 6 Pathologic mobility.
Figuras y tablas -
Analysis 4.6

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 6 Pathologic mobility.

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 7 Pathologic radiolucency.
Figuras y tablas -
Analysis 4.7

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 7 Pathologic radiolucency.

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 8 Pathological root resorption.
Figuras y tablas -
Analysis 4.8

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 8 Pathological root resorption.

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 9 Pulp canal obliteration.
Figuras y tablas -
Analysis 4.9

Comparison 4 Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy, Outcome 9 Pulp canal obliteration.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 5.1

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 1 Clinical failure.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 5.2

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 2 Radiological failure.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 3 Overall failure.
Figuras y tablas -
Analysis 5.3

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 3 Overall failure.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 4 Pain.
Figuras y tablas -
Analysis 5.4

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 4 Pain.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 5 Soft tissue pathology.
Figuras y tablas -
Analysis 5.5

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 5 Soft tissue pathology.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 6 Pathological mobility.
Figuras y tablas -
Analysis 5.6

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 6 Pathological mobility.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 7 Pathological radiolucency.
Figuras y tablas -
Analysis 5.7

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 7 Pathological radiolucency.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 8 Pathological root resorption.
Figuras y tablas -
Analysis 5.8

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 8 Pathological root resorption.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 9 Pulp canal obliteration.
Figuras y tablas -
Analysis 5.9

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 9 Pulp canal obliteration.

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 10 Dentin bridge formation.
Figuras y tablas -
Analysis 5.10

Comparison 5 Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy, Outcome 10 Dentin bridge formation.

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 6.1

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 1 Clinical failure.

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 6.2

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 2 Radiological failure.

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 6.3

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 3 Pain.

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 4 Soft tissue pathology.
Figuras y tablas -
Analysis 6.4

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 4 Soft tissue pathology.

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 5 Pathologic mobility.
Figuras y tablas -
Analysis 6.5

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 5 Pathologic mobility.

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 6 Pathological radiolucency.
Figuras y tablas -
Analysis 6.6

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 6 Pathological radiolucency.

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 7 Pathological root resorption.
Figuras y tablas -
Analysis 6.7

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 7 Pathological root resorption.

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 8 Pulp canal obliteration.
Figuras y tablas -
Analysis 6.8

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 8 Pulp canal obliteration.

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 9 Dentin bridge formation.
Figuras y tablas -
Analysis 6.9

Comparison 6 Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy, Outcome 9 Dentin bridge formation.

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 7.1

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 1 Clinical failure.

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 7.2

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 2 Radiological failure.

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 7.3

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 3 Pain.

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 4 Soft tissue pathology.
Figuras y tablas -
Analysis 7.4

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 4 Soft tissue pathology.

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 5 Pathologic mobility.
Figuras y tablas -
Analysis 7.5

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 5 Pathologic mobility.

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 6 Pathological radiolucency.
Figuras y tablas -
Analysis 7.6

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 6 Pathological radiolucency.

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 7 Pathological root resorption.
Figuras y tablas -
Analysis 7.7

Comparison 7 Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy, Outcome 7 Pathological root resorption.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 8.1

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 1 Clinical failure.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 8.2

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 2 Radiological failure.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 3 Overall failure.
Figuras y tablas -
Analysis 8.3

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 3 Overall failure.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 4 Pain.
Figuras y tablas -
Analysis 8.4

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 4 Pain.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 5 Soft tissue pathology.
Figuras y tablas -
Analysis 8.5

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 5 Soft tissue pathology.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 6 Pathological mobility.
Figuras y tablas -
Analysis 8.6

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 6 Pathological mobility.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 7 Pathological radiolucency.
Figuras y tablas -
Analysis 8.7

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 7 Pathological radiolucency.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 8 Pathological root resorption.
Figuras y tablas -
Analysis 8.8

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 8 Pathological root resorption.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 9 Pulp canal obliteration.
Figuras y tablas -
Analysis 8.9

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 9 Pulp canal obliteration.

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 10 Dentin bridge formation.
Figuras y tablas -
Analysis 8.10

Comparison 8 Calcium hydroxide pulpotomy versus formocresol pulpotomy, Outcome 10 Dentin bridge formation.

Comparison 9 Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 9.1

Comparison 9 Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy, Outcome 1 Clinical failure.

Comparison 9 Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 9.2

Comparison 9 Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy, Outcome 2 Radiological failure.

Comparison 9 Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy, Outcome 3 Overall failure.
Figuras y tablas -
Analysis 9.3

Comparison 9 Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy, Outcome 3 Overall failure.

Comparison 9 Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy, Outcome 4 Pathological root resorption.
Figuras y tablas -
Analysis 9.4

Comparison 9 Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy, Outcome 4 Pathological root resorption.

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 10.1

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 1 Clinical failure.

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 10.2

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 2 Radiological failure.

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 3 Overall failure.
Figuras y tablas -
Analysis 10.3

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 3 Overall failure.

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 4 Pain.
Figuras y tablas -
Analysis 10.4

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 4 Pain.

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 5 Pathological radiolucency.
Figuras y tablas -
Analysis 10.5

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 5 Pathological radiolucency.

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 6 Pathological root resorption.
Figuras y tablas -
Analysis 10.6

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 6 Pathological root resorption.

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 7 Pulp canal obliteration.
Figuras y tablas -
Analysis 10.7

Comparison 10 Ferric sulphate pulpotomy versus formocresol pulpotomy, Outcome 7 Pulp canal obliteration.

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 11.1

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 1 Clinical failure.

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 11.2

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 2 Radiological failure.

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 11.3

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 3 Pain.

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 4 Soft tissue pathology.
Figuras y tablas -
Analysis 11.4

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 4 Soft tissue pathology.

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 5 Adjacent tissue inflammation.
Figuras y tablas -
Analysis 11.5

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 5 Adjacent tissue inflammation.

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 6 Pathologic mobility.
Figuras y tablas -
Analysis 11.6

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 6 Pathologic mobility.

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 7 Pathologic radiolucency.
Figuras y tablas -
Analysis 11.7

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 7 Pathologic radiolucency.

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 8 Pathologic root resorption.
Figuras y tablas -
Analysis 11.8

Comparison 11 Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 8 Pathologic root resorption.

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 12.1

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 1 Clinical failure.

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 12.2

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 2 Radiological failure.

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 12.3

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 3 Pain.

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 4 Pathological radiolucency.
Figuras y tablas -
Analysis 12.4

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 4 Pathological radiolucency.

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 5 Pathological root resorption.
Figuras y tablas -
Analysis 12.5

Comparison 12 Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 5 Pathological root resorption.

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 13.1

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 1 Clinical failure.

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 13.2

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 2 Radiological failure.

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 13.3

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 3 Pain.

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 4 Pathological mobility.
Figuras y tablas -
Analysis 13.4

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 4 Pathological mobility.

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 5 Pathological root resorption.
Figuras y tablas -
Analysis 13.5

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 5 Pathological root resorption.

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 6 Pulp canal obliteration.
Figuras y tablas -
Analysis 13.6

Comparison 13 Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy, Outcome 6 Pulp canal obliteration.

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 14.1

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 1 Clinical failure.

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 14.2

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 2 Radiological failure.

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 14.3

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 3 Pain.

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 4 Soft tissue pathology.
Figuras y tablas -
Analysis 14.4

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 4 Soft tissue pathology.

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 5 Pathologic mobility.
Figuras y tablas -
Analysis 14.5

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 5 Pathologic mobility.

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 6 Pathologic radiolucency.
Figuras y tablas -
Analysis 14.6

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 6 Pathologic radiolucency.

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 7 Pathologic root resorption.
Figuras y tablas -
Analysis 14.7

Comparison 14 Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy, Outcome 7 Pathologic root resorption.

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 15.1

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 1 Clinical failure.

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 15.2

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 2 Radiological failure.

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 15.3

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 3 Pain.

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 4 Pathological mobility.
Figuras y tablas -
Analysis 15.4

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 4 Pathological mobility.

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 5 Pathological radiolucency.
Figuras y tablas -
Analysis 15.5

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 5 Pathological radiolucency.

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 6 Pathological root resorption.
Figuras y tablas -
Analysis 15.6

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 6 Pathological root resorption.

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 7 Pulp canal obliteration.
Figuras y tablas -
Analysis 15.7

Comparison 15 Diode laser pulpotomy versus electrosurgery pulpotomy, Outcome 7 Pulp canal obliteration.

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 16.1

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 1 Clinical failure.

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 16.2

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 2 Radiological failure.

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 16.3

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 3 Pain.

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 4 Soft tissue pathology.
Figuras y tablas -
Analysis 16.4

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 4 Soft tissue pathology.

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 5 Pathologic mobility.
Figuras y tablas -
Analysis 16.5

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 5 Pathologic mobility.

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 6 Pathologic radiolucency.
Figuras y tablas -
Analysis 16.6

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 6 Pathologic radiolucency.

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 7 Pathologic root resorption.
Figuras y tablas -
Analysis 16.7

Comparison 16 Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy, Outcome 7 Pathologic root resorption.

Comparison 17 Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 17.1

Comparison 17 Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy, Outcome 1 Clinical failure.

Comparison 17 Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy, Outcome 2 Pain.
Figuras y tablas -
Analysis 17.2

Comparison 17 Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy, Outcome 2 Pain.

Comparison 17 Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy, Outcome 3 Soft tissue pathology.
Figuras y tablas -
Analysis 17.3

Comparison 17 Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy, Outcome 3 Soft tissue pathology.

Comparison 17 Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy, Outcome 4 Pathologic mobility.
Figuras y tablas -
Analysis 17.4

Comparison 17 Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy, Outcome 4 Pathologic mobility.

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 1 Radiological failure.
Figuras y tablas -
Analysis 18.1

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 1 Radiological failure.

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 2 Pain.
Figuras y tablas -
Analysis 18.2

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 2 Pain.

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 3 Pathological mobility.
Figuras y tablas -
Analysis 18.3

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 3 Pathological mobility.

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 4 Pathological radiolucency.
Figuras y tablas -
Analysis 18.4

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 4 Pathological radiolucency.

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 5 Pathological radiolucency.
Figuras y tablas -
Analysis 18.5

Comparison 18 Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 5 Pathological radiolucency.

Comparison 19 Metapex versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 19.1

Comparison 19 Metapex versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 1 Clinical failure.

Comparison 19 Metapex versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 19.2

Comparison 19 Metapex versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 2 Radiological failure.

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 1 Clincal failure.
Figuras y tablas -
Analysis 20.1

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 1 Clincal failure.

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 20.2

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 2 Radiological failure.

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 20.3

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 3 Pain.

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 4 Soft tissue pathology.
Figuras y tablas -
Analysis 20.4

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 4 Soft tissue pathology.

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 5 Pathologic mobility.
Figuras y tablas -
Analysis 20.5

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 5 Pathologic mobility.

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 6 Pathological radiolucency.
Figuras y tablas -
Analysis 20.6

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 6 Pathological radiolucency.

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 7 Pathological root resorption.
Figuras y tablas -
Analysis 20.7

Comparison 20 Metapex pulpectomy versus Endoflas pulpectomy, Outcome 7 Pathological root resorption.

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 21.1

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 1 Clinical failure.

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 21.2

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 2 Radiological failure.

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 3 Overall failure.
Figuras y tablas -
Analysis 21.3

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 3 Overall failure.

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 4 Pain.
Figuras y tablas -
Analysis 21.4

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 4 Pain.

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 5 Pathological mobility.
Figuras y tablas -
Analysis 21.5

Comparison 21 Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy, Outcome 5 Pathological mobility.

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 1 Clinical failure.
Figuras y tablas -
Analysis 22.1

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 1 Clinical failure.

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 2 Radiological failure.
Figuras y tablas -
Analysis 22.2

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 2 Radiological failure.

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 3 Pain.
Figuras y tablas -
Analysis 22.3

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 3 Pain.

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 4 Pathologic mobility.
Figuras y tablas -
Analysis 22.4

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 4 Pathologic mobility.

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 5 Pathologic radiolucency.
Figuras y tablas -
Analysis 22.5

Comparison 22 Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy, Outcome 5 Pathologic radiolucency.

Summary of findings for the main comparison. Pulpotomy compared with pulpotomy using alternative medicament/technique for extensive decay in primary teeth

Pulpotomy compared with pulpotomy using alternative medicament/technique for extensive decay in primary teeth

Population: children with extensive decay in primary teeth

Settings: primary care

Intervention: pulpotomy with one type of medicament

Comparison: pulpotomy using alternative medicament or different technique

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Experimental

MTA versus formocresol

Clinical failure

(12 months)

28 per 1000

8.6 per 1000 (2.8 per 1000 to 26.0 per 1000)

RR 0.31 (0.10 to 0.93)

740

(12 studies)

⊕⊕⊕⊝
moderate1

Failure rate less than 3% across both the MTA and formocresol treatment groups. Seven of the 12 studies had no failures at 12 months.

No evidence of a difference in clinical failure at 6 months or 24 months

Radiological failure

(12 months)

50 per 1000

20.5 per 1000 (9.5 per 1000 to 44.5 per 1000)

RR 0.41 (0.19 to 0.89)

740 (12 studies)

⊕⊕⊕⊝
moderate1

Failure rate 5% across formocresol treatment groups and 2.1% across MTA treatment groups. Five of the 12 studies had no failures at 12 months.

Results similar at 6 and 24 months

MTA versus calcium hydroxide

Clinical failure (12 months)

14 per 1000

2.2 per 1000 (0.02 per 1000 to 9.8 per 1000)

RR 0.16 (0.04 to 0.70)

150 (4 studies)

⊕⊕⊕⊝
moderate1

Results similar at 24 months.

No evidence of a difference in clinical failure at 6 months

Radiological failure

(12 months)

351 per 1000

42.1 per 1000 (14 per 1000 to 126.4 per 1000)

RR 0.12 (0.04 to 0.36)

150 (4 studies)

⊕⊕⊝⊝
low2

Results similar at 6 and 24 months

Calcium hydroxide versus formocresol

Clinical failure (12 months)

115 per 1000

215 per 1000 (140.3 per 1000 to 332.4 per 1000)

RR 1.87 (1.22 to 2.89)

332 (6 studies)

⊕⊕⊕⊝
moderate1

Results similar at 6 months

No evidence of a difference in clinical failure at 24 months

Radiological failure (12 months)

253 per 1000

470.6 per 1000 (359.3 per 1000 to 617.3 per 1000)

RR 1.86 (1.42 to 2.44)

332 (6 studies)

⊕⊕⊕⊝
moderate1

Results similar at 6 and 24 months

Other comparisons assessed in more than one trial that had treatment failures

Clinical failure (at six, 12 and 24 months)

The quality of the evidence waslow for 4 comparisons3: laser versus ferric sulphate; Biodentine versus MTA; ferric sulphate versus formocresol; electrosurgery versus ferric sulphate; calcium hydroxide versus ferric sulphate.

The quality of the evidence was very low for 5 comparisons: NaOCl versus ferric sulphate4; laser versus electrosurgery4; MTA versus ferric sulphate5; ABS versus ferric sulphate6; EMD versus formocresol7.

Radiological failure (at six, 12 and 24 months)

The quality of the evidence waslow for 8 comparisons: NaOCl versus ferric sulphate2; MTA versus ferric sulphate3; Biodentine versus MTA3; ferric sulphate versus formocresol3; laser versus ferric sulphate3; electrosurgery versus ferric sulphate3; ABS versus ferric sulphate3; laser versus electrosurgery3; calcium hydroxide versus ferric sulphate (favouring ferric sulphate)3.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1. Downgraded 1 level due to high risk of bias
2. Downgraded 1 level due to high risk of bias and 1 level due to substantial inconsistency
3. Downgraded 1 level due to high risk of bias and 1 level due to imprecision
4. Downgraded 1 level due to high risk of bias and 2 levels due to imprecision
5. Downgraded 1 level due to high risk of bias, 1 level due to moderate inconsistency and 1 level due to imprecision
6. Downgraded 1 level due to high risk of bias and 2 levels due to very serious imprecision
7. Downgraded 1 level due to high risk of bias, 1 level due to substantial inconsistency and 1 level due to imprecision

Figuras y tablas -
Summary of findings for the main comparison. Pulpotomy compared with pulpotomy using alternative medicament/technique for extensive decay in primary teeth
Summary of findings 2. Pulpectomy compared with pulpectomy using alternative medicament for extensive decay in primary teeth

Pulpectomy compared with pulpectomy using alternative medicament for extensive decay in primary teeth

Population: children with extensive decay in primary teeth

Settings: primary care

Intervention: pulpectomy with 1 type of medicament

Comparison: pulpectomy using alternative medicament

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

Number of Participants
(studies)

Quality of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Experimental

Endoflas versus ZOE

Clinical failure (6 months)

128 per 1000

33.3 per 1000 (6.4 per 1000 to 192 per 1000)

RR 0.26 (0.05 to 1.50)

80 (2 studies)

⊕⊕⊕⊝
moderate1

One trial assessed failure at 12 months: RR 1.00, 95% 0.07 to 14.55

Radiological failure (6 months)

128 per 1000

33.3 per 1000 (6.4 per 1000 to 192 per 1000)

RR 0.26 (0.05 to 1.50)

80 (2 studies)

⊕⊕⊕⊝
moderate1

Metapex versus ZOE

Clinical failure (12 months)

97 per 1000

68.9 per 1000 (14.6 per 1000 to 323 per 1000)

RR 0.71 (0.15 to 3.33)

62 (2 studies)

⊕⊕⊕⊝
moderate1

Results similar at 6 months

Radiological failure (12 months)

129 per 1000

129 per 1000 (40 per 1000 to 421.8 per 1000)

RR 1.00 (0.31 to 3.27)

62 (2 studies)

⊕⊕⊕⊝
moderate1

Results similar at 6 months

Other comparisons assessed in more than one trial that had treatment failures

Clinical failure

The quality of the evidence was rated as low for 1 comparison: Vitapex versus ZOE (favouring ZOE)2

Radiological failure

The quality of the evidence was rated as low for 2 comparisons: Vitapex versus ZOE2 (favouring ZOE); calcium hydroxide versus ZOE3

1. Downgraded 1 level due to imprecision
2. Downgraded 2 levels due to very substantial inconsistency
3. Downgraded 1 level due to substantial inconsistency and 1 level due to imprecision

Figuras y tablas -
Summary of findings 2. Pulpectomy compared with pulpectomy using alternative medicament for extensive decay in primary teeth
Summary of findings 3. Direct pulp capping compared with direct pulp capping using alternative medicament for extensive decay in primary teeth

Direct pulp capping compared with direct pulp capping using alternative medicament for extensive decay in primary teeth

Population: children with extensive decay in primary teeth

Settings: primary care

Intervention: direct pulp capping with 1 type of medicament

Comparison: direct pulp capping using alternative medicament

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Experimental

Seven trials evaluated 22 comparisons of different medicaments for direct pulp capping. Each comparison was assessed by a single trial.

There were no clinical or radiological failures in two comparisons: acetone‐based total‐etch adhesive versus calcium hydroxide; MTA versus calcium hydroxide.

Clinical failure (at six, 12 and 24 months)

The quality of the evidence was assessed as low for 5 comparisons1: calcium hydroxide versus formocresol (favouring formocrescol), MTA versus 3Mix and MTA versus simvastatin (favouring MTA), 3Mix versus 3Mixtatin and 3Mixtatin versus simvastatin (favouring 3Mixtatin).

The quality of the evidence was rated as very low for all other comparisons.2

Radiological failure (at six, 12 and 24 months)

The quality of the evidence was rated as low for 1 comparison: calcium hydroxide versus formocresol1 (favouring formocresol).

The quality of the evidence was rated as very low for all other comparisons.2

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1. Downgraded 1 level due to risk of bias and 1 level due to imprecision
2. Downgraded 1 level due to risk of bias and 2 levels due to severe imprecision

Figuras y tablas -
Summary of findings 3. Direct pulp capping compared with direct pulp capping using alternative medicament for extensive decay in primary teeth
Table 1. Pulpotomy (FS + MTA) versus pulpotomy (MTA)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Pain

mean 22

1

Not estimable*

Soft tissue pathology

mean 22

1

Not estimable*

Pathological mobility

mean 22

1

Not estimable*

Pathological radiolucency

mean 22

1

3.46 (0.17 to 70.69)

Pathological root resorption

mean 22

1

2.75 (0.82 to 9.29)

Pulp canal obliteration

mean 22

1

0.83 (0.51 to 1.33)

*due to lack of events

Abbreviations ‐ CI: confidence interval; FS: ferric sulphate; MTA: mineral trioxide aggregate

Figuras y tablas -
Table 1. Pulpotomy (FS + MTA) versus pulpotomy (MTA)
Table 2. Pulpotomy (CEM cement) versus pulpotomy (MTA)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6, 12 and 18

1

Not estimable*

Radiological failure

6

1

Not estimable*

12

1

0.33 (0.04 to 2.94)

18

1

0.33 (0.04 to 2.94)

Pathological root resorption

6

1

Not estimable*

12

1

0.33 (0.04 to 2.94)

18

1

0.33 (0.04 to 2.94)

*due to lack of events

Abbreviations ‐ CEM: calcium‐enriched mixture; CI: confidence interval; MTA: mineral trioxide aggregate

Figuras y tablas -
Table 2. Pulpotomy (CEM cement) versus pulpotomy (MTA)
Table 3. Pulpotomy (MTA) versus pulpotomy (NaOCl)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6 and 12

1

Not estimable*

24

1

0.33 (0.01, 7.81)

Radiological failure

6 and 12

1

0.14 (0.01, 2.63)

24

1

0.33 (0.04, 2.99)

Overall failure

24

1

0.33 (0.04, 2.99)

Pain

6, 12 and 24 months

1

Not estimable*

Soft tissue pathology

6 and 12

1

Not estimable*

24

1

0.33 (0.01, 7.81)

Pathologic mobility

6, 12 and 24 months

1

Not estimable*

Pathologic radiolucency

6, 12 and 24 months

1

Not estimable*

Pathologicroot resorption

6 and 12

1

0.14 (0.01, 2.63)

24

1

0.33 (0.04, 2.99)

*due to lack of events

Abbreviations ‐ CI: confidence interval; MTA: mineral trioxide aggregate; NaOCl: sodium hypochlorite

Figuras y tablas -
Table 3. Pulpotomy (MTA) versus pulpotomy (NaOCl)
Table 4. Pulpotomy (MTA) versus pulpotomy (CH+NaOCl)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6 and 12

1

Not estimable*

Radiological failure

6

1

Not estimable*

12

1

0.09 (0.01, 1.58)

Soft tissue pathology

6 and 12

1

Not estimable*

Pathologic mobility

6 and 12

1

Not estimable*

Adjacent tissue inflammation

6 and 12

1

Not estimable*

Pathologic radiolucency

6

1

Not estimable*

12

1

0.14 (0.01, 2.66)

Pathologicroot resorption

6

1

Not estimable*

12

1

0.14 (0.01, 2.66)

Pulp canal obliteration

6

1

Not estimable*

12

1

0.44 (0.15, 1.29)

*due to lack of events

Abbreviations ‐ CI: confidence interval; MTA: mineral trioxide aggregate; CH: calcium hydroxyde; NaOCl; sodium hypochlorite

Figuras y tablas -
Table 4. Pulpotomy (MTA) versus pulpotomy (CH+NaOCl)
Table 5. Pulpotomy (MTA + NaOCl) versus pulpotomy (CH + NaOCl)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6 and 12

1

Not estimable*

Radiological failure

6

1

Not estimable*

12

1

0.20 (0.02, 1.61)

Soft tissue pathology

6 and 12

1

Not estimable*

Pathologic mobility

6 and 12

1

Not estimable*

Adjacent tissue inflammation

6 and 12

1

Not estimable*

Pathologic radiolucency

6

1

Not estimable*

12

1

0.14 (0.01, 2.66)

Pathologic root resorption

6

1

Not estimable*

12

1

0.33 (0.04, 3.03)

Pulp canal obliteration

6

1

Not estimable*

12

1

0.67 (0.27, 1.65)

*due to lack of events

Abbreviations ‐ CI: confidence interval; MTA: mineral trioxide aggregate; NaOCl; sodium hypochlorite; CH: calcium hydroxyde.

Figuras y tablas -
Table 5. Pulpotomy (MTA + NaOCl) versus pulpotomy (CH + NaOCl)
Table 6. Pulpotomy (MTA) versus pulpotomy (2% buffered glutaraldehyde)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Pain

6

1

0.06 (0.00, 0.98)

Soft tissue pathology

6

1

0.08 (0.00, 1.31)

Pathologic mobility

6

1

0.06 (0.00, 0.98)

Pathologic radiolucency

6

1

0.03 (0.00, 0.55)

Pathologic root resorption

6

1

0.05 (0.00, 0.78)

Pulp canal obliteration

6

1

0.11 (0.01, 1.98)

*due to lack of events

Abbreviations ‐ CI: confidence interval; MTA: mineral trioxide aggregate.

Figuras y tablas -
Table 6. Pulpotomy (MTA) versus pulpotomy (2% buffered glutaraldehyde)
Table 7. Pulpotomy (MTA) versus pulpotomy (ZOE)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

Not estimable*

24

1

0.20 (0.03 to 1.59)

Radiological failure

6

1

0.33 (0.01 to 7.81)

12

1

0.20 (0.01 to 3.97)

24

1

0.10 (0.01 to 0.72)

Overall failure

6

1

0.33 (0.01 to 7.81)

12

1

0.20 (0.01 to 3.97)

24

1

0.13 (0.02 to 0.93)

Pain

6

1

Not estimable*

12

1

Not estimable*

24

1

3.00 (0.13 to 70.30)

Pathological radiolucency

6

1

Not estimable*

12

1

Not estimable*

24

1

3.00 (0.13 to 70.30)

Pathological root resorption

6

1

0.33 (0.01 to 7.81)

12

1

0.33 (0.01 to 7.81)

24

1

0.08 (0.00 to 1.30)

Pulp canal obliteration

6

1

Not estimable*

12

1

3.00 (0.13 to 70.30)

24

1

11.0 (0.64 to 188.96)

Physiological root resorption

6

1

Not estimable*

12

1

Not estimable*

24

1

0.20 (0.01 to 3.97)

*due to lack of events

Abbreviations ‐ CI: confidence interval; MTA: mineral trioxide aggregate; ZOE: zinc oxide and eugenol

Figuras y tablas -
Table 7. Pulpotomy (MTA) versus pulpotomy (ZOE)
Table 8. Pulpotomy (diode laser + MTA) versus pulpotomy (FC + ZOE)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

15.7

1

Not estimable*

Radiological failure

15.7

1

4.00 (0.48 to 33.42)

Overall failure

15.7

1

2.00 (0.40 to 9.99)

Pathological radiolucency

15.7

1

3.00 (0.33 to 26.99)

Pathological root resorption

15.7

1

1.50 (0.27 to 8.25)

*due to lack of events

Abbreviations ‐ CI: confidence interval; FC: formocresol; MTA: mineral trioxide aggregate; ZOE: zinc oxide and eugenol

Figuras y tablas -
Table 8. Pulpotomy (diode laser + MTA) versus pulpotomy (FC + ZOE)
Table 9. Pulpotomy (MTA) versus pulpotomy (EMD)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6, 12 and 24

1

0.14 (0.01, 2.67)

Radiological failure

24

1

0.29 (0.06, 1.28)

Overall failure

6, 12 and 24

1

0.14 (0.01, 2.67)

Pain

6, 12 and 24

1

0.33 (0.01, 7.91)

Soft tissue pathology

6, 12 and 24

1

0.20 (0.01, 4.02)

Pathologic mobility

6, 12 and 24

1

0.20 (0.01, 4.02)

Pathologic radiolucency

24

1

0.40 (0.08, 1.93)

Pathologic root resorption

24

1

0.20 (0.01, 4.02)

Abbreviations ‐ CI: confidence interval; MTA: mineral trioxide aggregate; EMD: enamel matrix derivative

Figuras y tablas -
Table 9. Pulpotomy (MTA) versus pulpotomy (EMD)
Table 10. Pulpotomy (Tempophore) versus pulpotomy (MTA)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6 and 12

1

3.21 (0.14, 75.68)

Radiological failure

6

1

9.64 (0.54, 171.09)

12

1

2.69 (0.57, 12.70)

Pathological radiolucency

6

1

3.21 (0.14, 75.68)

12

1

2.15 (0.43, 10.79)

Pathological root resorption

6

1

6.44 (0.83, 50.11)

12

1

4.30 (1.00, 18.47)

Pulp canal obliteration

6

1

3.76 (0.85, 16.54)

12

1

1.61 (0.78, 3.33)

Dentine bridge formation

6

1

0.15 (0.01, 2.83)

12

1

0.07 (0.00, 1.19)

Abbreviation: CI: confidence interval

Figuras y tablas -
Table 10. Pulpotomy (Tempophore) versus pulpotomy (MTA)
Table 11. Pulpotomy (MTA) versus pulpotomy (MTA + NaOCl)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6 and 12

1

Not estimable*

Radiological failure

6 and 12

1

0.33 (0.01, 7.88)

Soft tissue pathology

6 and 12

1

Not estimable*

Pathologic mobility

6 and 12

1

Not estimable*

Adjacent tissue inflammation

6 and 12

1

Not estimable*

Pathologic radiolucency

6 and 12

1

Not estimable*

Pathologic root resorption

6 and 12

1

0.33 (0.01, 7.88)

Pulp canal obliteration

6

1

Not estimable*

12

1

0.67 (0.21, 2.13)

* due to lack of events

Abbreviations ‐ CI: confidence interval; MTA: mineral trioxide aggregate; NaOCl; sodium hypochlorite.

Figuras y tablas -
Table 11. Pulpotomy (MTA) versus pulpotomy (MTA + NaOCl)
Table 12. Pulpotomy (ProRoot MTA) versus pulpotomy (OrthoMTA)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

0.33 (0.01, 7.98)

Radiological failure

6

1

1.00 (0.06, 15.52)

12

1

0.50 (0.05, 5.33)

Pain

6 and 12

1

Not estimable*

Soft tissue pathology

6

1

Not estimable*

12

1

0.33 (0.01, 7.98)

Pathologic mobility

6 and 12

1

Not estimable*

Pathologic radiolucency

6

1

0.33 (0.01, 7.98)

12

1

0.20 (0.01, 4.06)

Pathologic root resorption

6

1

3.00 (0.13, 71.82)

12

1

1.00 (0.06, 15.52)

*due to lack of events

Abbreviation: CI: confidence interval.

Figuras y tablas -
Table 12. Pulpotomy (ProRoot MTA) versus pulpotomy (OrthoMTA)
Table 13. Pulpotomy (ProRoot MTA) versus pulpotomy (RetroMTA)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6 and 12

1

Not estimable*

Radiological failure

6 and 12

1

0.35 (0.04, 3.22)

Pain

6 and 12

1

Not estimable*

Soft tissue pathology

6 and 12

1

Not estimable*

Pathologic mobility

6 and 12

1

Not estimable*

Pathologic radiolucency

6 and 12

1

0.35 (0.01, 8.32)

Pathologic root resorption

6 and 12

1

0.35 (0.04, 3.22)

*due to lack of events

Abbreviation: CI: confidence interval.

Figuras y tablas -
Table 13. Pulpotomy (ProRoot MTA) versus pulpotomy (RetroMTA)
Table 14. Pulpotomy (OrthoMTA) versus pulpotomy (RetroMTA)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

3.13 (0.13, 74.85)

Radiological failure

6

1

0.35 (0.04, 3.22)

12

1

0.70 (0.12, 3.98)

Pain

6 and 12

1

Not estimable*

Soft tissue pathology

6

1

Not estimable*

12

1

3.13 (0.13, 74.85)

Pathologic mobility

6 and 12

1

Not estimable*

Pathologic radiolucency

6

1

1.04 (0.07, 16.19)

12

1

2.09 (0.20, 22.24)

Pathologic root resorption

6

1

0.15 (0.01, 2.81)

12

1

0.35 (0.04, 3.22)

*due to lack of events

Abbreviation: CI: confidence interval.

Figuras y tablas -
Table 14. Pulpotomy (OrthoMTA) versus pulpotomy (RetroMTA)
Table 15. Pulpotomy (CH) versus pulpotomy (PC)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

5.00 (0.26, 96.13)

12 and 24

1

13.00 (0.80, 212.02)

Radiological failure

6

1

13.00 (0.80, 212.02)

12

1

17.00 (1.07 to 270.41)

24

1

21.00 (1.34 to 328.86)

Soft tissue pathology

6

1

5.00 (0.26, 96.13)

12 and 24

1

13.00 (0.80, 212.02)

Pathologic mobility

6

1

5.00 (0.26, 96.13)

12 and 24

1

13.00 (0.80, 212.02)

Adjacent tissue inflammation

6, 12 and 24

1

Not estimable *

Pathologic radiolucency

6

1

13.00 (0.80, 212.02)

12

1

17.00 (1.07 to 270.41)

24

1

21.00 (1.34 to 328.86)

Pathologic root resorption

6

1

13.00 (0.80, 212.02)

12

1

17.00 (1.07 to 270.41)

24

1

21.00 (1.34 to 328.86)

Dentine bridge formation

6, 12 and 24

1

0.50 (0.11 to 2.33)

*due to lack of events

Abbreviations ‐ CI: confidence interval; CH: calcium hydroxide; PC: Portland cement.

Figuras y tablas -
Table 15. Pulpotomy (CH) versus pulpotomy (PC)
Table 16. Pulpotomy (CH) versus pulpotomy (MTA + NaOCl)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

3.00 (0.13, 70.92)

Radiological failure

6

1

5.00 (0.62, 40.36)

12

1

8.00 (1.06, 60.21)

Soft tissue pathology

6

1

Not estimable*

12

1

3.00 (0.13, 70.92)

Pathologic mobility

6 and 12

1

Not estimable*

Adjacent tissue inflammation

6 and 12

1

Not estimable*

Pathologic radiolucency

6

1

Not estimable*

12

1

15.00 (0.89, 251.77)

Pathologic root resorption

6

1

Not estimable*

12

17.00 (1.02, 282.30)

Pulp canal obliteration

6

1

Not estimable*

12

1

1.33 (0.52, 3.39)

*due to lack of events

Abbreviations ‐ CI: confidence interval; CH: calcium hydroxyde; MTA: mineral trioxide aggregate; NaOCl; sodium hypochlorite.

Figuras y tablas -
Table 16. Pulpotomy (CH) versus pulpotomy (MTA + NaOCl)
Table 17. Pulpotomy (Er:YAG laser) versus pulpotomy (CH)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

0.31 (0.01 to 7.48)

12

1

0.94 (0.60 to 14.52)

24

1

0.62 (0.11 to 3.56)

Radiological failure

12

1

0.56 (0.14 to 2.21)

24

1

0.31 (0.11 to 0.90)

Overall failure

12

1

0.56 (0.14 to 2.21)

24

1

0.31 (0.11 to 0.90)

Pain

6, 12 and 24

1

Not estimable*

Soft tissue pathology

6, 12 and 24

1

Not estimable*

Pathological mobility

6, 12 and 24

1

Not estimable*

Pathological radiolucency

12

1

0.31 (0.01 to 7.48)

24

1

0.62 (0.11 to 3.56)

Pathological root resorption

12

1

0.94 (0.60 to 14.52)

24

1

0.62 (0.11 to 3.56)

*due to lack of events

Abbreviations ‐ CI: confidence interval; Er:YAG: erbium:yttrium‐aluminium garnet; CH: calcium hydroxide.

Figuras y tablas -
Table 17. Pulpotomy (Er:YAG laser) versus pulpotomy (CH)
Table 18. Pulpotomy (CH/iodoform) versus pulpotomy (CH)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

1.41 (0.77 to 2.58)

12

1

1.13 (0.82 to 1.54)

Radiological failure

6

1

1.33 (0.89 to 2.00)

12

1

1.17 (0.87 to 1.59)

Pain

6

1

1.72 (0.45 to 6.61)

12

1

1.03 (0.33 to 3.23)

Soft tissue pathology

6

1

1.55 (0.28 to 8.65)

12

1

1.03 (0.22 to 4.74)

Pathological radiolucency

6 and 12

1

5.15 (0.26 to 103.31)

Pathological root resorption

6

1

1.72 (0.45 to 6.61)

12

1

1.29 (0.38 to 4.37)

CI: confidence interval; CH: calcium hydroxide.

Figuras y tablas -
Table 18. Pulpotomy (CH/iodoform) versus pulpotomy (CH)
Table 19. Pulpotomy (CH + NaOCl) versus pulpotomy (CH)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

0.33 (0.01, 7.88)

Radiological failure

6

1

0.09 (0.01, 1.58)

12

1

0.63 (0.23, 1.70)

Soft tissue pathology

6

1

Not estimable*

12

1

0.33 (0.01, 7.88)

Pathologic mobility

6 and 12

1

Not estimable*

Adjacent tissue inflammation

6 and 12

1

Not estimable*

Pathologic radiolucency

6

1

Not estimable*

12

1

0.43 (0.12, 1.51)

Pathologic root resorption

6

1

Not estimable*

12

0.38 (0.11, 1.28)

Pulp canal obliteration

6

1

Not estimable*

12

1

1.13 (0.50, 2.53)

*due to lack of events

Abbreviations ‐ CI: confidence interval; CH: calcium hydroxide; NaOCl: sodium hypochlorite.

Figuras y tablas -
Table 19. Pulpotomy (CH + NaOCl) versus pulpotomy (CH)
Table 20. Pulpotomy (FS) versus pulpotomy (buffered glutaraldehyde)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Pain

6

1

0.25 (0.06, 1.08)

Soft tissue pathology

6

1

0.33 (0.07, 1.52)

Pathologic mobility

6

1

0.75 (0.30, 1.90)

Pathologic radiolucency

6

1

1.14 (0.69, 1.90)

Pathologic root resorption

6

1

1.20 (0.61, 2.34)

Pulp canal obliteration

6

1

0.11 (0.01, 1.98)

*due to lack of events

Abbreviations ‐ CI: confidence interval; FS: ferric sulfate.

Figuras y tablas -
Table 20. Pulpotomy (FS) versus pulpotomy (buffered glutaraldehyde)
Table 21. Pulpotomy (FS) versus pulpotomy (ZOE)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6 and 12

1

Not estimable*

24

1

1.20 (0.42 to 3.43)

Radiological failure

6

1

0.33 (0.01 to 7.81)

12

1

0.20 (0.01 to 3.97)

24

1

0.60 (0.26 to 1.40)

Overall failure

6

1

0.33 (0.01 to 7.81)

12

1

0.20 (0.01 to 3.97)

24

1

0.38 (0.11 to 1.25)

Pain

6, 12 and 24

1

Not estimable*

Pathological radiolucency

6, 12 and 24

1

Not estimable*

Pathological root resorption

6

1

0.33 (0.01 to 7.81)

12

1

0.33 (0.01 to 7.81)

24

1

0.17 (0.02 to 1.29)

Physiological root resorption

6 and 12

1

Not estimable*

24

1

1.50 (0.27 to 8.22)

Pulp canal obliteration

6, 12 and 24

1

Not estimable*

*due to lack of events

Abbreviations ‐ CI: confidence interval; FS: ferric sulphate; ZOE: zinc oxide and eugenol

Figuras y tablas -
Table 21. Pulpotomy (FS) versus pulpotomy (ZOE)
Table 22. Pulpotomy (Er:YAG laser) versus pulpotomy (FS)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

3.19 (0.13 to 76.37)

24

1

5.31 (0.26 to 107.86)

Radiological failure

12

1

0.46 (0.13 to 1.66)

24

1

0.61 (0.19 to 1.94)

Overall failure

12

1

0.46 (0.13 to 1.66)

24

1

0.61 (0.19 to 1.94)

Pain

6, 12 and 24

1

Not estimable*

Soft tissue pathology

6, 12 and 24

1

Not estimable*

Pathological mobility

6, 12 and 24

1

Not estimable*

Pathological radiolucency

12

1

0.15 (0.01 to 2.86)

24

1

0.71 (0.12 to 4.06)

Pathological root resorption

12

1

0.53 (0.05 to 5.67)

24

1

1.06 (0.16 to 7.25)

*due to lack of events

Abbreviations ‐ CI: confidence interval; Er:YAG: erbium:yttrium‐aluminium garnet; FS: ferric sulphate

Figuras y tablas -
Table 22. Pulpotomy (Er:YAG laser) versus pulpotomy (FS)
Table 23. Pulpotomy (FS + MTA) versus pulpotomy (FS)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Pain

mean 22

1

0.25 (0.01 to 6.08)

Soft tissue pathology

mean 22

1

0.25 (0.01 to 6.08)

Pathological mobility

mean 22

1

0.15 (0.01 to 3.09)

Adjacent tissue inflammation

mean 22

1

0.25 (0.01 to 6.08)

Pathological radiolucency

mean 22

1

0.29 (0.01 to 6.92)

Pathological root resorption

mean 22

1

0.60 (0.31 to 1.19)

Pulp canal obliteration

mean 22

1

1.39 (0.78 to 2.49)

CI: confidence interval; FS: ferric sulphate; MTA: mineral trioxide aggregate

Figuras y tablas -
Table 23. Pulpotomy (FS + MTA) versus pulpotomy (FS)
Table 24. Pulpotomy (PC) versus pulpotomy (FC)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6, 12 and 24

1

2.00 (0.19, 21.06)

Radiological failure

24

1

0.80 (0.23, 2.73)

Overall failure

6, 12 and 24

1

2.00 (0.19, 21.06)

Pain

6, 12 and 24

1

1.00 (0.07, 15.36)

Soft tissue pathology

6, 12 and 24

1

2.00 (0.19, 21.06)

Pathologic mobility

6, 12 and 24

1

3.00 (0.13, 71.22)

Pathologic radiolucency

24

1

1.00 (0.22, 4.62)

Pathologic root resorption

24

1

0.50 (0.05, 5.27)

Abbreviations ‐ CI: confidence interval; PC: Portland cement; FC: formocresol

Figuras y tablas -
Table 24. Pulpotomy (PC) versus pulpotomy (FC)
Table 25. Pulpotomy (PC) versus pulpotomy (EMD)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6, 12 and 24

1

0.67 (0.12, 3.75)

Radiological failure

24

1

0.57 (0.18, 1.78)

Overall failure

6, 12 and 24

1

0.67 (0.12, 3.75)

Pain

6, 12 and 24

1

1.00 (0.07, 15.36)

Soft tissue pathology

6, 12 and 24

1

1.00 (0.15, 6.71)

Pathologic mobility

6, 12 and 24

1

0.50 (0.05, 5.27)

Pathologic radiolucency

24

1

0.60 (0.16, 2.32)

Pathologic root resorption

24

1

0.50 (0.05, 5.27)

*due to lack of events

Abbreviations ‐ CI: confidence interval; PC: Portland cement; EMD: enamel matrix derivative

Figuras y tablas -
Table 25. Pulpotomy (PC) versus pulpotomy (EMD)
Table 26. Pulpotomy (glutaraldehyde + CH) versus pulpotomy (glutaraldehyde + ZOE)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

12

1

2.90 (0.32 to 26.38)

Radiological failure

12

1

1.11 (0.46 to 2.67)

Pain

12

1

Not estimable*

Pathological radiolucency

12

1

0.97 (0.39 to 2.43)

Pathological root resorption

12

1

0.97 (0.15 to 6.44)

*due to lack of events

Abbreviations ‐ CH: calcium hydroxide; CI: confidence interval; ZOE: zinc oxide and eugenol

Figuras y tablas -
Table 26. Pulpotomy (glutaraldehyde + CH) versus pulpotomy (glutaraldehyde + ZOE)
Table 27. Pulpotomy (electrofulguration + CH) versus pulpotomy (electrofulguration + ZOE)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

0.83 (0.26, 2.73)

Radiological failure

6

1

0.94 (0.47, 1.88)

Overall failure

6

1

0.94 (0.47, 1.88)

Pain

6

1

Not estimable*

Soft tissue pathology

6

1

0.83 (0.26, 2.73)

Pathologic mobility

6

1

Not estimable*

Pathologic radiolucency

6

1

1.04 (0.43, 2.51)

Pathologic root resorption

6

1

0.75 (0.28, 2.02)

Pulp canal obliteration

6

1

1.04 (0.16, 6.80)

*due to lack of events

Abbreviations ‐ CI: confidence interval; CH: calcium hydroxide; ZOE: zinc oxide eugenol

Figuras y tablas -
Table 27. Pulpotomy (electrofulguration + CH) versus pulpotomy (electrofulguration + ZOE)
Table 28. Pulpotomy (electrosurgery) versus pulpotomy (FC)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

9

1

3.00 (0.13 to 71.22)

Radiological failure

9

1

5.00 (0.62 to 40.64)

Pain

6

1

Not estimable*

Soft tissue pathology

6

1

3.00 (0.13 to 71.22)

Pathological mobility

6

1

Not estimable*

Pathological radiolucency

6

1

5.00 (0.25 to 100.54)

Pathological root resorption

6

1

5.00 (0.25 to 100.54)

*due to lack of events

Abbreviations ‐ CI: confidence interval; FC: formocresol

Figuras y tablas -
Table 28. Pulpotomy (electrosurgery) versus pulpotomy (FC)
Table 29. Pulpotomy (Biodentine) versus pulpotomy (Tempophore)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6 and 12

1

1.08 (0.07, 16.36)

Radiological failure

6 and 12

1

0.54 (0.11, 2.70)

Pathological radiolucency

6

1

2.16 (0.21, 22.38)

12

1

0.54 (0.11, 2.70)

Pathological root resorption

6

1

0.36 (0.08, 1.62)

12

1

0.31 (0.07, 1.35)

Pulp canal obliteration

6

1

1.39 (0.61, 3.17)

12

1

1.08 (0.60, 1.94)

Dentine bridge formation

6

1

Not estimable*

12

1

11.85 (0.69, 203.86)

*due to lack of events

Abbreviations ‐ CI: confidence interval

Figuras y tablas -
Table 29. Pulpotomy (Biodentine) versus pulpotomy (Tempophore)
Table 30. Pulpotomy (CH/iodoform) versus pulpotomy (FC)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

16.41 (2.30 to 117.26)

12

1

9.11 (3.04 to 27.31)

Radiological failure

6

1

24.06 (3.44 to 168.43)

12

1

9.11 (3.04 to 27.31)

Pain

6

1

5.47 (0.67 to 44.34)

12

1

5.47 (0.67 to 44.34)

Soft tissue pathology

6

1

7.64 (0.41 to 142.35)

12

1

7.64 (0.41 to 142.35)

Pathological radiolucency

6

1

2.19 (0.21 to 22.99)

12

1

2.19 (0.21 to 22.99)

Pathological root resorption

6

1

12.00 (0.69 to 208.77)

12

1

5.47 (0.67 to 44.34)

Abbreviations ‐ CH: calcium hydroxide; CI: confidence interval; FC: formocresol

Figuras y tablas -
Table 30. Pulpotomy (CH/iodoform) versus pulpotomy (FC)
Table 31. Pulpotomy (ZOE) versus pulpotomy (FC)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

Not estimable*

24

1

0.83 (0.29 to 2.38)

Radiological failure

6

1

3.00 (0.13 to 70.30)

12

1

5.00 (0.25 to 99.17)

24

1

1.67 (0.71 to 3.89)

Overall failure

6

1

3.00 (0.13 to 70.30)

12

1

5.00 (0.25 to 99.17)

24

1

2.67 (0.80 to 8.90)

Pain

6, 12 and 24

1

Not estimable*

Pathological radiolucency

6, 12 and 24

1

Not estimable*

Pathological root resorption

6

1

3.00 (0.13 to 70.30)

12

1

3.00 (0.13 to 70.30)

24

1

6.00 (0.78 to 46.29)

Pulp canal obliteration

6

1

Not estimable*

12

1

0.20 (0.01 to 3.97)

24

1

0.20 (0.01 to 3.97)

Physiological root resorption

6

1

Not estimable*

12

1

Not estimable*

24

1

2.00 (0.19 to 20.67)

*due to lack of events

Abbreviations ‐ CI: confidence interval; FC: formocresol; ZOE: zinc oxide and eugenol

Figuras y tablas -
Table 31. Pulpotomy (ZOE) versus pulpotomy (FC)
Table 32. Pulpotomy (Er:YAG laser) versus pulpotomy (FC)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

3.19 (0.13 to 76.37)

24

1

2.13 (0.20 to 22.70)

Radiological failure

6

1

Not estimable*

12

1

1.60 (0.28 to 9.13)

24

1

1.06 (0.28 to 4.01)

Overall failure

6

1

Not estimable*

12

1

1.60 (0.28 to 9.13)

24

1

1.06 (0.28 to 4.01)

Pain

6, 12 and 24

1

Not estimable*

Soft tissue pathology

6

1

Not estimable*

12

1

Not estimable*

24

1

0.35 (0.01 to 8.49)

Pathological mobility

6, 12 and 24

1

Not estimable*

Pathological radiolucency

6

1

Not estimable*

12

1

0.21 (0.01 to 4.31)

24

1

1.06 (0.16 to 7.25)

Pathological root resorption

6

1

Not estimable*

12

1

3.19 (0.13 to 76.37)

24

1

1.06 (0.16 to 7.25)

*due to lack of events

Abbreviations ‐ CI: confidence interval; Er:YAG: erbium:yttrium‐aluminium garnet; FC: formocresol

Figuras y tablas -
Table 32. Pulpotomy (Er:YAG laser) versus pulpotomy (FC)
Table 33. Pulpotomy (diode laser) versus pulpotomy (FC)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

0.33 (0.01, 7.95)

Radiological failure

6

1

1.67 (0.43, 6.51)

12

1

2.00 (0.75, 5.33)

*due to lack of events

Abbreviations ‐ CI: confidence interval; FC: formocresol.

Figuras y tablas -
Table 33. Pulpotomy (diode laser) versus pulpotomy (FC)
Table 34. Pulpotomy (ABS) versus pulpotomy (FC)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6 and 12

1

0.33 (0.01, 7.58)

24

1

1.00 (0.16, 6.20)

Radiological failure

6 and 12

1

1.00 (0.16, 6.20)

24

1

0.67 (0.13, 3.44)

Pain

6 and 12

1

0.33 (0.01, 7.58)

24

1

1.00 (0.16, 6.20)

Soft tissue pathology

6, 12 and 24 months

1

0.33 (0.01, 7.58)

Pathologic mobility

6, 12 and 24 months

1

0.33 (0.01, 7.58)

Pathological radiolucency

6 and 12

1

Not estimable*

Pathological root resorption

6 and 12

1

1.00 (0.16, 6.20)

24

1

0.67 (0.13, 3.44)

*due to lack of events

Abbreviation ‐ CI: confidence interval

Figuras y tablas -
Table 34. Pulpotomy (ABS) versus pulpotomy (FC)
Table 35. Pulpectomy (Sealapex) versus pulpectomy (CH)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

1.00 (0.07 to 14.90)

12

1

0.50 (0.10 to 2.43)

Radiological failure

6 and 12

1

0.50 (0.10 to 2.43)

Pain

6 and 12

1

1.00 (0.07 to 14.90)

Pathological mobility

6 and 12

1

1.00 (0.07 to 14.90)

Pathological radiolucency

6 and 12

1

0.20 (0.01 to 3.92)

Pathological root resorption

6 and 12

1

5.00 (0.26 to 98.00)

Filling material anomaly

6 and 12

1

Not estimable*

*due to lack of events

Abbreviations ‐ CI: confidence interval; Sealapex: eugenol‐free CH; CH: calcium hydroxide.

Figuras y tablas -
Table 35. Pulpectomy (Sealapex) versus pulpectomy (CH)
Table 36. Pulpectomy (Vitapex) versus pulpectomy (CH)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

0.33 (0.01 to 7.72)

12

1

0.11 (0.01 to 1.94)

Radiological failure

6 and 12

1

0.11 (0.01 to 1.94)

Pain

6 and 12

1

0.33 (0.01 to 7.72)

Pathological mobility

6 and 12

1

0.33 (0.01 to 7.72)

Pathological radiolucency

6 and 12

1

0.20 (0.01 to 3.92)

Pathological root resorption

6 and 12

1

Not estimable*

Filling material anomaly

6 and 12

1

3.00 (0.13 to 69.52)

*due to lack of events

Abbreviations ‐ CI: confidence interval; Vitapex: CH/iodoform; CH: calcium hydroxide.

Figuras y tablas -
Table 36. Pulpectomy (Vitapex) versus pulpectomy (CH)
Table 37. Pulpectomy (Vitapex) versus pulpectomy (Sealapex)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

0.33 (0.01 to 7.72)

12

1

0.20 (0.01 to 3.92)

Radiological failure

6 and 12

1

0.20 (0.01 to 3.92)

Pain

6 and 12

1

0.33 (0.01 to 7.72)

Pathological mobility

6 and 12

1

0.33 (0.01 to 7.72)

Pathological radiolucency

6 and 12

1

Not estimable*

Pathological root resorption

6 and 12

1

0.20 (0.01 to 3.92)

Filling material anomaly

6 and 12

1

3.00 (0.13 to 69.52)

*due to lack of events

Abbreviations ‐ CI: confidence interval; Vitapex: CH/iodoform; CH: calcium hydroxide; Sealapex: eugenol‐free CH.

Figuras y tablas -
Table 37. Pulpectomy (Vitapex) versus pulpectomy (Sealapex)
Table 38. Pulpectomy (Vitapex) versus pulpectomy (3Mix)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

1.0 (0.07 to 15.12)

Radiological failure

6

1

1.25 (0.38 to 4.12)

12

1

1.83 (0.80 to 4.19)

Pain

6

1

Not estimable*

12

1

3.00 (0.13 to 70.30)

Soft tissue pathology

6

1

Not estimable*

12

1

1.0 (0.07 to 15.12)

Pathological mobility

6 and 12

1

Not estimable*

Pathological radiolucency

6

1

1.50 (0.27 to 8.22)

12

1

2.75 (1.01 to 7.48)

Pathological root resorption

6 and 12

1

0.20 (0.01 to 3.97)

Pulp canal obliteration

6

1

Not estimable*

12

1

0.20 (0.01 to 3.97)

*due to lack of events

Abbreviations ‐ CI: confidence interval; Vitapex: CH/iodoform; CH: calcium hydroxide; 3Mix: ciprofloxacin + metronidazole + minocycline.

Figuras y tablas -
Table 38. Pulpectomy (Vitapex) versus pulpectomy (3Mix)
Table 39. Pulpectomy (Vitapex) versus pulpectomy (MPRCF)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12

1

21.79 (1.32, 360.78)

Radiological failure

6

1

6.63 (0.35, 125.41)

12

1

42.63 (2.65, 685.54)

*due to lack of events

Abbreviations ‐ CI: confidence interval; Vitapex: CH/iodoform; MPRCF: ZOE (zinc oxide eugenol), calcium hydroxide, iodoform.

Figuras y tablas -
Table 39. Pulpectomy (Vitapex) versus pulpectomy (MPRCF)
Table 40. Pulpotomy (FS) versus pulpectomy (Sedanol)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Pain

24

1

1.80 (0.07 to 43.88)

Soft tissue pathology

24

1

4.21 (0.22 to 80.70)

Pathological radiolucency

24

1

0.60 (0.25 to 1.46)

Pathological root resorption

24

1

21.04 (1.28 to 346.39)

Pulp canal obliteration

24

1

27.05 (1.66 to 441.49)

Abbreviations ‐ CI: confidence interval; FS: ferric sulphate; Sedanol=ZOE: zinc oxide and eugenol.

Figuras y tablas -
Table 40. Pulpotomy (FS) versus pulpectomy (Sedanol)
Table 41. Pulpotomy (3Mix) versus pulpectomy (3Mix)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

3.00 (0.13, 70.83)

12

1

5.00 (0.25, 99.95)

Pain

6

1

3.00 (0.13, 70.83)

12

1

5.00 (0.25, 99.95)

Soft tissue pathology

6

1

Not estimable*

12

1

3.00 (0.13, 70.83)

Pathologic mobility

6 and 12

1

3.00 (0.13, 70.83)

Pathologic radiolucency

6

1

23.00 (1.42, 373.46)

12

1

11.00 (0.64, 190.53)

*due to lack events

Abbreviations ‐ CI: confidence interval; 3Mix: ciprofloxacin + metronidazole + minocycline.

Figuras y tablas -
Table 41. Pulpotomy (3Mix) versus pulpectomy (3Mix)
Table 42. Direct pulp capping (CH) versus direct pulp capping (FC)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

24

1

3.83 (1.68 to 8.74)

Radiological failure

24

1

3.11 (1.61 to 6.02)

Pain

6

1

7.00 (0.37 to 132.66)

12

1

9.00 (0.50 to 163.59)

24

1

4.00 (0.89 to 18.06)

Soft tissue pathology

6

1

7.00 (0.37 to 132.66)

12

1

2.5 (0.50 to 12.39)

24

1

1.8 (0.64 to 5.06)

Pathological radiolucency

6

1

Not estimable*

12

1

4.00 (0.46 to 34.75)

24

1

5.00 (1.14 to 21.86)

Pathological root resorption

6

1

Not estimable*

12

1

3.33 (0.96 to 11.51)

24

1

2.00 (0.87 to 4.60)

*due to lack of events

Abbreviations ‐ CH: calcium hydroxide; CI: confidence interval; FC: formocresol.

Figuras y tablas -
Table 42. Direct pulp capping (CH) versus direct pulp capping (FC)
Table 43. Direct pulp capping (total‐etching with 36% phosphoric acid + acetone‐based total‐etch adhesive) versus direct pulp capping (CH)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Radiological failure

6

1

Not estimable*

12

1

3.00 (0.13 to 69.52)

24

1

7.00 (0.38 to 127.33)

Pain

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pathological radiolucency

6

1

Not estimable*

12

1

3.00 (0.13 to 69.52)

24

1

7.00 (0.38 to 127.33)

Pathological root resorption

6, 12 and 24

1

Not estimable*

*due to lack of events

Abbreviations ‐ CH: calcium hydroxide; CI: confidence interval

Figuras y tablas -
Table 43. Direct pulp capping (total‐etching with 36% phosphoric acid + acetone‐based total‐etch adhesive) versus direct pulp capping (CH)
Table 44. Direct pulp capping (self etch adhesive system + acetone‐based total‐etch adhesive) versus direct pulp capping (CH)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6, 12 and 24

1

3.00 (0.13 to 69.52)

Radiological failure

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pain

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pathological radiolucency

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pathological root resorption

6, 12 and 24

1

Not estimable*

*due to lack of events

Abbreviations ‐ CH: calcium hydroxide; CI: confidence interval

Figuras y tablas -
Table 44. Direct pulp capping (self etch adhesive system + acetone‐based total‐etch adhesive) versus direct pulp capping (CH)
Table 45. Direct pulp capping (total‐etching with 36% phosphoric acid + acetone‐based total‐etch adhesive) versus direct pulp capping (acetone‐based total‐etch adhesive)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Radiological failure

6 and 12

1

3.00 (0.13 to 69.52)

24

1

7.00 (0.38 to 127.33)

Pain

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pathological radiolucency

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pathological root resorption

6, 12 and 24

1

Not estimable*

*due to lack of events

Abbreviation ‐ CI: confidence interval.

Figuras y tablas -
Table 45. Direct pulp capping (total‐etching with 36% phosphoric acid + acetone‐based total‐etch adhesive) versus direct pulp capping (acetone‐based total‐etch adhesive)
Table 46. Direct pulp capping (self etch adhesive system + acetone‐based total‐etch adhesive) versus direct pulp capping (acetone‐based total‐etch adhesive)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6, 12 and 24

1

3.00 (0.13 to 69.52)

Radiological failure

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pain

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pathological radiolucency

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pathological root resorption

6, 12 and 24

1

Not estimable*

*due to lack of events

Abbreviation ‐ CI: confidence interval

Figuras y tablas -
Table 46. Direct pulp capping (self etch adhesive system + acetone‐based total‐etch adhesive) versus direct pulp capping (acetone‐based total‐etch adhesive)
Table 47. Direct pulp capping (total‐etching with 36% phosphoric acid + acetone‐based total‐etch adhesive) versus direct pulp capping (non‐rinse conditioner + acetone‐based total‐etch adhesive)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Radiological failure

6

1

Not estimable*

12

1

3.00 (0.13 to 69.52)

24

1

7.00 (0.38 to 127.33)

Pain

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pathological radiolucency

6

1

Not estimable*

12

1

3.00 (0.13 to 69.52)

24

1

7.00 (0.38 to 127.33)

Pathological root resorption

6, 12 and 24

1

Not estimable*

*due to lack of events

Abbreviations ‐ CI: confidence interval.

Figuras y tablas -
Table 47. Direct pulp capping (total‐etching with 36% phosphoric acid + acetone‐based total‐etch adhesive) versus direct pulp capping (non‐rinse conditioner + acetone‐based total‐etch adhesive)
Table 48. Direct pulp capping (self etch adhesive system + acetone‐based total‐etch adhesive) versus direct pulp capping (non‐rinse conditioner + acetone‐based total‐etch adhesive)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6, 12 and 24

1

3.00 (0.13 to 69.52)

Radiological failure

6

1

Not estimable*

12 and 24

1

1.00 (0.07 to 14.90)

Pain

6

1

Not estimable*

12 and 24

1

3.00 (0.13 to 69.52)

Pathological radiolucency

6

1

Not estimable*

12 and 24

1

1.00 (0.07 to 14.90)

Pathological root resorption

6, 12 and 24

1

Not estimable*

*due to lack of events

Abbreviation ‐ CI: confidence interval.

Figuras y tablas -
Table 48. Direct pulp capping (self etch adhesive system + acetone‐based total‐etch adhesive) versus direct pulp capping (non‐rinse conditioner + acetone‐based total‐etch adhesive)
Table 49. Direct pulp capping (self etch adhesive system + acetone‐based total‐etch adhesive) versus direct pulp capping (total‐etching with 36% phosphoric acid + acetone‐based total‐etch adhesive)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

6

1

3.00 (0.13 to 69.52)

12 and 24

1

1.00 (0.07 to 14.90)

Radiological failure

6

1

0.33 (0.01 to 7.72)

12

1

1.00 (0.07 to 14.90)

24

1

0.33 (0.04 to 2.94)

Pain

6

1

Not estimable*

12

1

3.00 (0.13 to 69.52)

24

1

1.00 (0.07 to 14.90)

Pathological radiolucency

6

1

Not estimable*

12

1

1.00 (0.07 to 14.90)

24

1

0.33 (0.04 to 2.94)

Pathological root resorption

6, 12 and 24

1

Not estimable*

*due to lack of events

Abbreviation ‐ CI: confidence interval.

Figuras y tablas -
Table 49. Direct pulp capping (self etch adhesive system + acetone‐based total‐etch adhesive) versus direct pulp capping (total‐etching with 36% phosphoric acid + acetone‐based total‐etch adhesive)
Table 50. Direct pulp capping (Dycal) versus direct pulp capping (Dentogen)

Outcome

Time point (months)

No. of studies

Risk ratio (95% CI)

Clinical failure

1, 3, 6

1

5.00 (0.26, 98.00)

9

1

7.00 (0.38, 127.32)

12

1

4.00 (0.49, 32.72)

Radiological failure

1, 3, 6

1

5.00 (0.26, 98.00)

9

1

3.00 (0.34, 26.45)

12

1

1.67 (0.46, 6.06)

Pain

1, 3, 6, 9

1

Not estimable*

12

1

3.00 (0.13, 69.52)

Soft tissue pathology

1, 3, 6, 9

1

5.00 (0.26, 98.00)

12

1

2.00 (0.20, 20.33)

Pathologic mobility

1, 3, 6, 9

1

5.00 (0.26, 98.00)

12

1

2.00 (0.20, 20.33)

Pathologic radiolucency

1, 3, 6

1

5.00 (0.26, 98.00)

9

1

3.00 (0.34, 26.45)

12

1

1.33 (0.34, 5.21)

Pathologic root resorption

1, 3, 6

1

5.00 (0.26, 98.00)

9

1

2.00 (0.20, 20.33)

12

1.33 (0.34, 5.21)

*due to lack of events

Abbreviation ‐ CI: confidence interval.

Figuras y tablas -
Table 50. Direct pulp capping (Dycal) versus direct pulp capping (Dentogen)
Comparison 1. Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

14

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

13

1048

Risk Ratio (M‐H, Fixed, 95% CI)

0.37 [0.07, 1.89]

1.2 12 months

12

740

Risk Ratio (M‐H, Fixed, 95% CI)

0.31 [0.10, 0.93]

1.3 24 months

9

548

Risk Ratio (M‐H, Fixed, 95% CI)

0.47 [0.18, 1.19]

2 Radiological failure Show forest plot

13

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

12

922

Risk Ratio (M‐H, Fixed, 95% CI)

0.38 [0.17, 0.86]

2.2 12 months

12

740

Risk Ratio (M‐H, Fixed, 95% CI)

0.41 [0.19, 0.89]

2.3 24 months

9

548

Risk Ratio (M‐H, Fixed, 95% CI)

0.42 [0.22, 0.80]

3 Overall failure Show forest plot

7

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

6

328

Risk Ratio (M‐H, Fixed, 95% CI)

0.23 [0.04, 1.32]

3.2 12 months

6

328

Risk Ratio (M‐H, Fixed, 95% CI)

0.48 [0.17, 1.36]

3.3 24 months

7

368

Risk Ratio (M‐H, Fixed, 95% CI)

0.50 [0.25, 1.01]

4 Pain Show forest plot

7

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

6

390

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

4.2 12 months

6

410

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.03, 2.18]

4.3 24 months

4

290

Risk Ratio (M‐H, Fixed, 95% CI)

0.71 [0.14, 3.56]

5 Soft tissue pathology Show forest plot

8

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

7

410

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

5.2 12 months

7

430

Risk Ratio (M‐H, Fixed, 95% CI)

0.22 [0.05, 1.01]

5.3 24 months

5

310

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.04, 3.10]

6 Pathological mobility Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

5

250

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.2 12 months

4

200

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.97]

6.3 24 months

3

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7 Pathological radiolucency Show forest plot

14

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

13

1010

Risk Ratio (M‐H, Fixed, 95% CI)

0.54 [0.27, 1.08]

7.2 12 months

11

652

Risk Ratio (M‐H, Fixed, 95% CI)

0.43 [0.19, 0.98]

7.3 24 months

8

460

Risk Ratio (M‐H, Fixed, 95% CI)

0.55 [0.25, 1.22]

8 Pathological root resorption Show forest plot

12

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

8.1 6 months

11

866

Risk Ratio (M‐H, Fixed, 95% CI)

0.47 [0.18, 1.21]

8.2 12 months

9

508

Risk Ratio (M‐H, Fixed, 95% CI)

0.26 [0.07, 1.03]

8.3 24 months

6

338

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.08, 0.81]

9 Pulp canal obliteration Show forest plot

9

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

9.1 6 months

9

712

Risk Ratio (M‐H, Fixed, 95% CI)

1.52 [1.00, 2.30]

9.2 12 months

7

410

Risk Ratio (M‐H, Fixed, 95% CI)

1.70 [0.81, 3.57]

9.3 24 months

6

338

Risk Ratio (M‐H, Fixed, 95% CI)

2.05 [1.07, 3.94]

10 Dentin bridge formation Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

10.1 6 months

3

322

Risk Ratio (M‐H, Fixed, 95% CI)

18.16 [3.63, 90.91]

10.2 12 months

2

70

Risk Ratio (M‐H, Fixed, 95% CI)

6.0 [0.76, 47.22]

10.3 24 months

2

70

Risk Ratio (M‐H, Fixed, 95% CI)

6.0 [0.76, 47.22]

11 Physiological root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

11.1 6 months

2

170

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

11.2 12 months

2

170

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

11.3 24 months

2

170

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.81]

Figuras y tablas -
Comparison 1. Mineral trioxide aggregate (MTA) pulpotomy versus full strength or 1:5 diluted formocresol pulpotomy
Comparison 2. Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

7

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

6

538

Risk Ratio (M‐H, Fixed, 95% CI)

0.70 [0.09, 5.64]

1.2 12 months

5

432

Risk Ratio (M‐H, Fixed, 95% CI)

0.45 [0.12, 1.68]

1.3 24 months

3

290

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.04, 3.14]

2 Radiological failure Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

4

362

Risk Ratio (M‐H, Fixed, 95% CI)

0.29 [0.05, 1.79]

2.2 12 months

5

432

Risk Ratio (M‐H, Fixed, 95% CI)

0.28 [0.08, 0.98]

2.3 24 months

3

290

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.06, 0.67]

3 Pain Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

3.2 12 months

3

260

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.03, 2.18]

3.3 24 months

2

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.04, 3.14]

4 Soft tissue pathology Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

4.2 12 months

3

260

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.03, 2.18]

4.3 24 months

2

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

5 Pathological radiolucency Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

4

388

Risk Ratio (M‐H, Fixed, 95% CI)

0.16 [0.01, 2.95]

5.2 12 months

4

332

Risk Ratio (M‐H, Fixed, 95% CI)

0.61 [0.16, 2.38]

5.3 24 months

2

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.45 [0.11, 1.95]

6 Pathological root resorption Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

3

316

Risk Ratio (M‐H, Fixed, 95% CI)

0.11 [0.01, 1.95]

6.2 12 months

3

260

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

6.3 24 months

2

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.13 [0.02, 0.98]

7 Pulp canal obliteration Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

2

192

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.2 12 months

2

192

Risk Ratio (M‐H, Fixed, 95% CI)

12.76 [0.79, 206.70]

Figuras y tablas -
Comparison 2. Mineral trioxide aggregate (MTA) pulpotomy versus full strength formocresol pulpotomy
Comparison 3. Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

8

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

8

560

Risk Ratio (M‐H, Fixed, 95% CI)

0.16 [0.01, 3.06]

1.2 12 months

7

308

Risk Ratio (M‐H, Fixed, 95% CI)

0.16 [0.02, 1.28]

1.3 24 months

6

258

Risk Ratio (M‐H, Fixed, 95% CI)

0.51 [0.18, 1.42]

2 Radiological failure Show forest plot

8

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

8

560

Risk Ratio (M‐H, Fixed, 95% CI)

0.41 [0.17, 1.03]

2.2 12 months

7

308

Risk Ratio (M‐H, Fixed, 95% CI)

0.56 [0.20, 1.53]

2.3 24 months

6

258

Risk Ratio (M‐H, Fixed, 95% CI)

0.67 [0.31, 1.46]

3 Pain Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

4

200

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.2 12 months

3

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.3 24 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

3.0 [0.13, 70.30]

4 Soft tissue pathology Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

5

220

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.2 12 months

4

170

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.02, 1.65]

4.3 24 months

3

120

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.72]

5 Pathological mobility Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

4

180

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.97]

5.3 24 months

2

80

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Pathological radiolucency Show forest plot

9

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

9

622

Risk Ratio (M‐H, Fixed, 95% CI)

0.61 [0.30, 1.27]

6.2 12 months

7

320

Risk Ratio (M‐H, Fixed, 95% CI)

0.36 [0.13, 1.02]

6.3 24 months

6

270

Risk Ratio (M‐H, Fixed, 95% CI)

0.6 [0.23, 1.57]

7 Pathological root resorption Show forest plot

8

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

8

550

Risk Ratio (M‐H, Fixed, 95% CI)

0.70 [0.24, 1.99]

7.2 12 months

6

248

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.05, 1.14]

7.3 24 months

4

148

Risk Ratio (M‐H, Fixed, 95% CI)

0.43 [0.10, 1.92]

8 Pulp canal obliteration Show forest plot

7

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

8.1 6 months

7

520

Risk Ratio (M‐H, Fixed, 95% CI)

1.52 [1.00, 2.30]

8.2 12 months

5

218

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.44, 2.26]

8.3 24 months

5

218

Risk Ratio (M‐H, Fixed, 95% CI)

1.97 [0.99, 3.89]

Figuras y tablas -
Comparison 3. Mineral trioxide aggregate (MTA) pulpotomy versus 1:5 diluted formocresol pulpotomy
Comparison 4. Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

4

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.08 [0.00, 1.31]

1.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.97]

1.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.52 [0.20, 1.39]

2 Radiological failure Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

4

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.06 [0.01, 0.40]

2.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.71 [0.15, 3.44]

2.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.58 [0.25, 1.36]

3 Overall failure Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

4

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.06 [0.01, 0.40]

3.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.71 [0.15, 3.44]

3.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.78 [0.32, 1.89]

4 Pain Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

3

160

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 4.00]

4.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Soft tissue pathology Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 4.00]

6 Pathologic mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.08 [0.00, 1.31]

7 Pathologic radiolucency Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

3

160

Risk Ratio (M‐H, Fixed, 95% CI)

0.03 [0.00, 0.48]

7.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.81]

7.3 24 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.97]

8 Pathological root resorption Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

8.1 6 months

4

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.07 [0.01, 0.53]

8.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.97]

8.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.56 [0.12, 2.51]

9 Pulp canal obliteration Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

9.1 6 months

3

140

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

9.2 12 months

2

80

Risk Ratio (M‐H, Fixed, 95% CI)

3.0 [0.13, 70.30]

9.3 24 months

2

80

Risk Ratio (M‐H, Fixed, 95% CI)

1.57 [0.47, 5.27]

Figuras y tablas -
Comparison 4. Mineral trioxide aggregate (MTA) pulpotomy versus ferric sulphate (FS) pulpotomy
Comparison 5. Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

4

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.85]

1.2 12 months

4

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.16 [0.04, 0.70]

1.3 24 months

5

284

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.12, 0.52]

2 Radiological failure Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

4

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.08 [0.02, 0.41]

2.2 12 months

4

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.12 [0.04, 0.36]

2.3 24 months

5

284

Risk Ratio (M‐H, Fixed, 95% CI)

0.14 [0.08, 0.26]

3 Overall failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

68

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.92]

3.2 12 months

2

68

Risk Ratio (M‐H, Fixed, 95% CI)

0.34 [0.10, 1.19]

3.3 24 months

2

68

Risk Ratio (M‐H, Fixed, 95% CI)

0.42 [0.18, 0.95]

4 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 24 months

2

196

Risk Ratio (M‐H, Fixed, 95% CI)

0.41 [0.09, 1.73]

5 Soft tissue pathology Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

3

122

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.02, 1.62]

5.2 12 months

3

122

Risk Ratio (M‐H, Fixed, 95% CI)

0.12 [0.02, 0.62]

5.3 24 months

4

256

Risk Ratio (M‐H, Fixed, 95% CI)

0.17 [0.06, 0.47]

6 Pathological mobility Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

3

122

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.02, 1.62]

6.2 12 months

3

122

Risk Ratio (M‐H, Fixed, 95% CI)

0.09 [0.01, 0.66]

6.3 24 months

4

256

Risk Ratio (M‐H, Fixed, 95% CI)

0.09 [0.01, 0.66]

7 Pathological radiolucency Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

4

162

Risk Ratio (M‐H, Fixed, 95% CI)

0.10 [0.02, 0.50]

7.2 12 months

4

162

Risk Ratio (M‐H, Fixed, 95% CI)

0.14 [0.04, 0.47]

7.3 24 months

5

296

Risk Ratio (M‐H, Fixed, 95% CI)

0.08 [0.03, 0.22]

8 Pathological root resorption Show forest plot

6

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

8.1 6 months

5

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.10 [0.02, 0.39]

8.2 12 months

5

190

Risk Ratio (M‐H, Fixed, 95% CI)

0.07 [0.02, 0.29]

8.3 24 months

6

324

Risk Ratio (M‐H, Fixed, 95% CI)

0.08 [0.03, 0.18]

9 Pulp canal obliteration Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

9.1 6 months

3

120

Risk Ratio (M‐H, Fixed, 95% CI)

7.77 [1.56, 38.69]

9.2 12 months

3

120

Risk Ratio (M‐H, Fixed, 95% CI)

2.01 [0.97, 4.17]

9.3 24 months

4

254

Risk Ratio (M‐H, Fixed, 95% CI)

2.05 [1.01, 4.19]

10 Dentin bridge formation Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

10.1 6 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.05, 0.84]

10.2 12 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

0.8 [0.37, 1.74]

10.3 24 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

0.8 [0.37, 1.74]

Figuras y tablas -
Comparison 5. Mineral trioxide aggregate (MTA) pulpotomy versus calcium hydroxide pulpotomy
Comparison 6. Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 4.02]

1.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 4.02]

1.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 4.02]

2 Radiological failure Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.5 [0.10, 2.56]

3 Pain Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

3.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

3.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

4 Soft tissue pathology Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 4.02]

4.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 4.02]

4.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 4.02]

5 Pathologic mobility Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

5.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

5.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

6 Pathological radiolucency Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.67 [0.12, 3.75]

7 Pathological root resorption Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.2 12 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.3 24 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.91]

8 Pulp canal obliteration Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

8.1 6 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

0.73 [0.49, 1.08]

8.2 12 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

0.83 [0.60, 1.14]

8.3 24 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

0.96 [0.71, 1.29]

9 Dentin bridge formation Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

9.1 6 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

0.56 [0.13, 2.43]

9.2 12 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

1.5 [0.61, 3.71]

9.3 24 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

1.5 [0.61, 3.71]

Figuras y tablas -
Comparison 6. Mineral trioxide aggregate (MTA) pulpotomy versus Portland cement pulpotomy
Comparison 7. Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

4

234

Risk Ratio (M‐H, Fixed, 95% CI)

1.72 [0.42, 6.99]

1.2 12 months

2

144

Risk Ratio (M‐H, Fixed, 95% CI)

0.75 [0.16, 3.62]

2 Radiological failure Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

4

234

Risk Ratio (M‐H, Fixed, 95% CI)

2.40 [0.65, 8.84]

2.2 12 months

2

144

Risk Ratio (M‐H, Fixed, 95% CI)

1.08 [0.22, 5.27]

3 Pain Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

3

180

Risk Ratio (M‐H, Fixed, 95% CI)

5.0 [0.26, 98.00]

4 Soft tissue pathology Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

3

180

Risk Ratio (M‐H, Fixed, 95% CI)

5.0 [0.26, 98.00]

5 Pathologic mobility Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

3

180

Risk Ratio (M‐H, Fixed, 95% CI)

5.0 [0.26, 98.00]

6 Pathological radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

2

144

Risk Ratio (M‐H, Fixed, 95% CI)

3.46 [0.15, 81.36]

6.2 12 months

2

144

Risk Ratio (M‐H, Fixed, 95% CI)

1.09 [0.19, 6.27]

7 Pathological root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

2

144

Risk Ratio (M‐H, Fixed, 95% CI)

2.32 [0.22, 24.09]

7.2 12 months

2

144

Risk Ratio (M‐H, Fixed, 95% CI)

1.12 [0.30, 4.19]

Figuras y tablas -
Comparison 7. Biodentine pulpotomy versus Mineral trioxide aggregate (MTA) pulpotomy
Comparison 8. Calcium hydroxide pulpotomy versus formocresol pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

6

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

6

332

Risk Ratio (M‐H, Fixed, 95% CI)

1.98 [1.17, 3.37]

1.2 12 months

6

332

Risk Ratio (M‐H, Fixed, 95% CI)

1.87 [1.22, 2.89]

1.3 24 months

3

150

Risk Ratio (M‐H, Fixed, 95% CI)

2.18 [0.78, 6.11]

2 Radiological failure Show forest plot

6

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

4

154

Risk Ratio (M‐H, Fixed, 95% CI)

15.48 [3.86, 62.06]

2.2 12 months

6

332

Risk Ratio (M‐H, Fixed, 95% CI)

1.86 [1.42, 2.44]

2.3 24 months

3

150

Risk Ratio (M‐H, Fixed, 95% CI)

3.63 [1.73, 7.61]

3 Overall failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 12 months

2

120

Risk Ratio (M‐H, Fixed, 95% CI)

2.41 [0.80, 7.21]

3.2 24 months

2

120

Risk Ratio (M‐H, Fixed, 95% CI)

2.93 [1.35, 6.34]

4 Pain Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

4

276

Risk Ratio (M‐H, Fixed, 95% CI)

3.18 [0.35, 29.08]

4.2 12 months

4

276

Risk Ratio (M‐H, Fixed, 95% CI)

6.30 [1.15, 34.40]

5 Soft tissue pathology Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

5

306

Risk Ratio (M‐H, Fixed, 95% CI)

5.14 [0.63, 42.25]

5.2 12 months

5

306

Risk Ratio (M‐H, Fixed, 95% CI)

6.77 [1.23, 37.10]

5.3 24 months

2

124

Risk Ratio (M‐H, Fixed, 95% CI)

2.64 [0.51, 13.55]

6 Pathological mobility Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

4

238

Risk Ratio (M‐H, Fixed, 95% CI)

1.21 [0.18, 8.19]

6.2 12 months

4

238

Risk Ratio (M‐H, Fixed, 95% CI)

1.14 [0.40, 3.31]

6.3 24 months

2

124

Risk Ratio (M‐H, Fixed, 95% CI)

9.0 [0.53, 153.79]

7 Pathological radiolucency Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

3

128

Risk Ratio (M‐H, Fixed, 95% CI)

3.78 [0.64, 22.17]

7.2 12 months

5

306

Risk Ratio (M‐H, Fixed, 95% CI)

1.90 [0.67, 5.40]

7.3 24 months

2

124

Risk Ratio (M‐H, Fixed, 95% CI)

3.24 [0.79, 13.28]

8 Pathological root resorption Show forest plot

6

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

8.1 6 months

4

154

Risk Ratio (M‐H, Fixed, 95% CI)

11.87 [2.33, 60.40]

8.2 12 months

6

332

Risk Ratio (M‐H, Fixed, 95% CI)

6.25 [2.04, 19.14]

8.3 24 months

3

150

Risk Ratio (M‐H, Fixed, 95% CI)

4.59 [1.33, 15.81]

9 Pulp canal obliteration Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

9.1 6 months

2

56

Risk Ratio (M‐H, Fixed, 95% CI)

4.0 [0.47, 33.75]

9.2 12 months

3

140

Risk Ratio (M‐H, Fixed, 95% CI)

2.68 [0.91, 7.95]

10 Dentin bridge formation Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

10.1 6 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

13.0 [1.81, 93.60]

10.2 12 months

2

60

Risk Ratio (M‐H, Fixed, 95% CI)

14.0 [1.95, 100.26]

Figuras y tablas -
Comparison 8. Calcium hydroxide pulpotomy versus formocresol pulpotomy
Comparison 9. Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

122

Risk Ratio (M‐H, Fixed, 95% CI)

3.4 [0.14, 81.38]

1.2 12 months

2

122

Risk Ratio (M‐H, Fixed, 95% CI)

3.41 [0.37, 31.61]

1.3 24 months

2

122

Risk Ratio (M‐H, Fixed, 95% CI)

3.44 [0.90, 13.18]

2 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 12 months

2

122

Risk Ratio (M‐H, Fixed, 95% CI)

1.28 [0.53, 3.13]

2.2 24 months

2

122

Risk Ratio (M‐H, Fixed, 95% CI)

1.97 [1.04, 3.75]

3 Overall failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 12 months

2

122

Risk Ratio (M‐H, Fixed, 95% CI)

1.28 [0.53, 3.13]

3.2 24 months

2

122

Risk Ratio (M‐H, Fixed, 95% CI)

1.97 [1.04, 3.75]

4 Pathological root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 12 months

2

122

Risk Ratio (M‐H, Fixed, 95% CI)

0.57 [0.05, 6.05]

4.2 24 months

2

122

Risk Ratio (M‐H, Fixed, 95% CI)

2.29 [0.60, 8.66]

Figuras y tablas -
Comparison 9. Calcium hydroxide pulpotomy versus ferric sulphate pulpotomy
Comparison 10. Ferric sulphate pulpotomy versus formocresol pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

7

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

7

394

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.15, 6.87]

1.2 12 months

7

394

Risk Ratio (M‐H, Fixed, 95% CI)

1.38 [0.45, 4.27]

1.3 24 months

5

258

Risk Ratio (M‐H, Fixed, 95% CI)

0.83 [0.40, 1.70]

2 Radiological failure Show forest plot

7

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

6

294

Risk Ratio (M‐H, Fixed, 95% CI)

0.79 [0.32, 1.92]

2.2 12 months

7

394

Risk Ratio (M‐H, Fixed, 95% CI)

1.33 [0.73, 2.42]

2.3 24 months

5

258

Risk Ratio (M‐H, Fixed, 95% CI)

1.26 [0.71, 2.24]

3 Overall failure Show forest plot

5

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

4

184

Risk Ratio (M‐H, Fixed, 95% CI)

0.53 [0.12, 2.37]

3.2 12 months

5

284

Risk Ratio (M‐H, Fixed, 95% CI)

1.16 [0.51, 2.64]

3.3 24 months

4

228

Risk Ratio (M‐H, Fixed, 95% CI)

1.49 [0.74, 3.01]

4 Pain Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

4

230

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.58]

4.2 12 months

4

230

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.58]

4.3 24 months

4

230

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.85]

5 Pathological radiolucency Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 12 months

4

230

Risk Ratio (M‐H, Fixed, 95% CI)

1.8 [0.40, 8.17]

5.2 24 months

4

230

Risk Ratio (M‐H, Fixed, 95% CI)

2.2 [0.51, 9.50]

6 Pathological root resorption Show forest plot

6

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

5

214

Risk Ratio (M‐H, Fixed, 95% CI)

0.67 [0.12, 3.84]

6.2 12 months

6

314

Risk Ratio (M‐H, Fixed, 95% CI)

1.64 [0.53, 5.08]

6.3 24 months

5

258

Risk Ratio (M‐H, Fixed, 95% CI)

1.21 [0.50, 2.96]

7 Pulp canal obliteration Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

3

134

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.2 12 months

3

134

Risk Ratio (M‐H, Fixed, 95% CI)

0.94 [0.54, 1.64]

7.3 24 months

2

78

Risk Ratio (M‐H, Fixed, 95% CI)

1.24 [0.28, 5.54]

Figuras y tablas -
Comparison 10. Ferric sulphate pulpotomy versus formocresol pulpotomy
Comparison 11. Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 12 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

4.39 [0.22, 87.82]

2 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.55 [0.22, 1.39]

2.2 12 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.42 [0.17, 1.02]

3 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.2 12 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Soft tissue pathology Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.2 12 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.29 [0.01, 6.91]

5 Adjacent tissue inflammation Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.2 12 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.31 [0.03, 2.91]

6 Pathologic mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.2 12 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7 Pathologic radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.88 [0.06, 13.35]

7.2 12 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.56 [0.07, 4.17]

8 Pathologic root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

8.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.51 [0.18, 1.42]

8.2 12 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

0.38 [0.15, 1.01]

Figuras y tablas -
Comparison 11. Sodium hypochlorite (NaOCl) pulpotomy versus ferric sulfate (FS) pulpotomy
Comparison 12. Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.23 [0.04, 1.30]

1.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.02, 1.62]

2 Radiological failure Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

3

130

Risk Ratio (M‐H, Fixed, 95% CI)

0.89 [0.38, 2.12]

2.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.91 [0.44, 1.92]

3 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.03, 1.60]

4 Pathological radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.03, 2.08]

5 Pathological root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

1.5 [0.29, 7.73]

Figuras y tablas -
Comparison 12. Diode laser pulpotomy versus ferric sulfate (FS) pulpotomy
Comparison 13. Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.56 [0.13, 2.34]

2 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

1.25 [0.38, 4.12]

3 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.56 [0.13, 2.34]

4 Pathological mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Pathological root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

2.2 [0.54, 8.88]

6 Pulp canal obliteration Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figuras y tablas -
Comparison 13. Electrosurgery pulpotomy versus ferric sulfate (FS) pulpotomy
Comparison 14. Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

1.25 [0.37, 4.27]

2 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.16, 6.20]

2.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.88 [0.34, 2.23]

3 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.15, 6.71]

4 Soft tissue pathology Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

1.5 [0.27, 8.43]

5 Pathologic mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Pathologic radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.67 [0.12, 3.75]

7 Pathologic root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

5.0 [0.26, 96.13]

7.2 12 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.31, 3.23]

Figuras y tablas -
Comparison 14. Ankaferd Blood Stopper (ABS) versus Ferric Sulfate (FS) pulpotomy
Comparison 15. Diode laser pulpotomy versus electrosurgery pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.70]

2 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.64 [0.19, 2.18]

3 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.2 [0.01, 3.70]

4 Pathological mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Pathological radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Pathological root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.64 [0.19, 2.18]

7 Pulp canal obliteration Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figuras y tablas -
Comparison 15. Diode laser pulpotomy versus electrosurgery pulpotomy
Comparison 16. Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 12 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

1.29 [0.33, 5.08]

2.2 12 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

1.86 [0.52, 6.59]

3 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.2 12 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Soft tissue pathology Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.2 12 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Pathologic mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.2 12 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Pathologic radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.2 12 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7 Pathologic root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

1.29 [0.33, 5.08]

7.2 12 months

2

150

Risk Ratio (M‐H, Fixed, 95% CI)

1.86 [0.52, 6.59]

Figuras y tablas -
Comparison 16. Sodium hypochlorite (NaOCl) pulpotomy versus 1:5 diluted formocresol pulpotomy
Comparison 17. Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.8 [0.23, 2.83]

2 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

0.4 [0.08, 1.92]

3 Soft tissue pathology Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

2.0 [0.19, 21.06]

4 Pathologic mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

5.0 [0.26, 96.13]

Figuras y tablas -
Comparison 17. Enamel matrix derivative (EMD) pulpotomy versus formocresol pulpotomy
Comparison 18. Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

2.5 [0.50, 12.50]

2 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.14, 6.90]

3 Pathological mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.14, 6.90]

4 Pathological radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

110

Risk Ratio (M‐H, Fixed, 95% CI)

1.5 [0.26, 8.72]

5 Pathological radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.03, 2.08]

Figuras y tablas -
Comparison 18. Calcium hydroxide pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy
Comparison 19. Metapex versus zinc oxide eugenol (ZOE) pulpectomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

62

Risk Ratio (M‐H, Fixed, 95% CI)

0.6 [0.08, 4.29]

1.2 12 months

2

62

Risk Ratio (M‐H, Fixed, 95% CI)

0.71 [0.15, 3.33]

2 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

62

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.31, 3.27]

2.2 12 months

2

62

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.31, 3.27]

Figuras y tablas -
Comparison 19. Metapex versus zinc oxide eugenol (ZOE) pulpectomy
Comparison 20. Metapex pulpectomy versus Endoflas pulpectomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clincal failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

92

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.58]

2 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

92

Risk Ratio (M‐H, Fixed, 95% CI)

2.02 [0.79, 5.15]

3 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

92

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.58]

4 Soft tissue pathology Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

92

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.58]

5 Pathologic mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

92

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Pathological radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

6.1 6 months

2

92

Risk Ratio (M‐H, Fixed, 95% CI)

2.02 [0.79, 5.15]

7 Pathological root resorption Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

7.1 6 months

2

92

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figuras y tablas -
Comparison 20. Metapex pulpectomy versus Endoflas pulpectomy
Comparison 21. Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

4

287

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.84]

1.2 12 months

4

287

Risk Ratio (M‐H, Fixed, 95% CI)

4.75 [1.21, 18.55]

2 Radiological failure Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

4

287

Risk Ratio (M‐H, Fixed, 95% CI)

2.36 [0.86, 6.50]

2.2 12 months

4

287

Risk Ratio (M‐H, Fixed, 95% CI)

6.56 [2.58, 16.67]

3 Overall failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

140

Risk Ratio (M‐H, Fixed, 95% CI)

1.89 [0.63, 5.66]

3.2 12 months

2

140

Risk Ratio (M‐H, Fixed, 95% CI)

2.56 [0.89, 7.32]

4 Pain Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

3

180

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.2 12 months

3

180

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Pathological mobility Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

3

180

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.01, 7.84]

5.2 12 months

3

180

Risk Ratio (M‐H, Fixed, 95% CI)

1.0 [0.07, 15.18]

Figuras y tablas -
Comparison 21. Vitapex pulpectomy versus zinc oxide and eugenol (ZOE) pulpectomy
Comparison 22. Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Clinical failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 6 months

2

80

Risk Ratio (M‐H, Fixed, 95% CI)

0.26 [0.05, 1.50]

2 Radiological failure Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 6 months

2

80

Risk Ratio (M‐H, Fixed, 95% CI)

0.26 [0.05, 1.50]

3 Pain Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

3.1 6 months

2

80

Risk Ratio (M‐H, Fixed, 95% CI)

0.26 [0.05, 1.50]

4 Pathologic mobility Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

4.1 6 months

2

80

Risk Ratio (M‐H, Fixed, 95% CI)

0.16 [0.02, 1.25]

5 Pathologic radiolucency Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

5.1 6 months

2

80

Risk Ratio (M‐H, Fixed, 95% CI)

0.64 [0.11, 3.63]

Figuras y tablas -
Comparison 22. Endoflas pulpectomy versus zinc oxide eugenol (ZOE) pulpectomy