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Cochrane Database of Systematic Reviews

Anestésicos tópicos para el control del dolor durante la reparación de laceraciones dérmicas

Información

DOI:
https://doi.org/10.1002/14651858.CD005364.pub3Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 22 febrero 2017see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Anestesia

Copyright:
  1. Copyright © 2017 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Autores

  • Baraa O Tayeb

    Correspondencia a: Pain Research, Education and Policy (PREP) Program, Department of Public Health and Community Medicine, Tufts University School of Medicine, Boston, USA

    [email protected]

    [email protected]

    College of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia

  • Anthony Eidelman

    Department of Neurosurgery, Division of Neuromedicine Pain, University of Rochester, Rochester, USA

  • Cristy L Eidelman

    Department of Clinical Pharmacology,Toxicology, and Individualized Pediatric Therapeutics, Children’s Mercy Hospital, Kansas City, USA

  • Ewan D McNicol

    Pain Research, Education and Policy (PREP) Program, Department of Public Health and Community Medicine, Tufts University School of Medicine, Boston, USA

    Department of Anesthesiology and Perioperative Medicine, Tufts Medical Center, Boston, USA

    Department of Pharmacy, Tufts Medical Center, Boston, USA

  • Daniel B Carr

    Pain Research, Education and Policy (PREP) Program, Department of Public Health and Community Medicine, Tufts University School of Medicine, Boston, USA

    Department of Anesthesiology, Tufts Medical Center, Boston, USA

Contributions of authors

Conceiving the review: Daniel Carr (DC).
Co‐ordinating the original review and the 2011 update review: Anthony Eidelman(AE) and DC.

Co‐ordinating the current 2016 updated review: DC and Baraa Tayeb (BT).
Undertaking manual searches: BT.
Screening search results: BT, DC, AE, Cristy Eidelman (CE) and Ewan McNicol (EM).
Organizing retrieval of papers: BT.
Screening retrieved papers against inclusion criteria: BT, AE, CE and EM.
Appraising the quality of papers: DC, AE, CE, BT and EM.
Abstracting data from papers: DC, AE, CE, BT and EM.
Writing to authors of papers for additional information: AE and BT.
Providing additional data about papers: BT and AE.
Obtaining and screening data from unpublished studies: AE.
Managing data for the review: BT and EM.
Entering data into Review Manager and reviewing entered data (RevMan 5.3): BT and CE.
Analysing RevMan 5.3 statistical data: BT.
Performing other statistical analyses not using RevMan 5.3: BT, AE, CE and EM.
Interpreting data: AE, CE, EM, BT and DC.
Performing statistical analysis: BT and EM.
Writing the review: BT, EM, CE, AE and DC.
Securing funding for the original review: DC.
Performing previous work that served as the foundation of the present study: EM, CE, AE and DC.
Serving as guarantor for the review (one review author): BT.
Taking responsibility for reading and checking the review before submission: BT, EM, DC and CE.

Sources of support

Internal sources

  • None, Other.

External sources

  • No sources of support supplied

Declarations of interest

Baraa O Tayeb: none known.

Anthony Eidelman: none known.

Cristy L Eidelman: none known.

Ewan D McNicol: none known.

Daniel B Carr has served as an officer, committee member and lecturer for various professional organizations and community medical centres. None of these activities involved topical application of local anaesthetics. He had patents issued (2012 to 2016) that reflected his work before joining Javelin/Hospira. These patents relate to multi‐valent (e.g. opioid‐tachykinin) peptides. None of them relate to topical local anaesthetics applied for any purpose, nor does Dr. Carr have any financial interest in these or any other patents.

Acknowledgements

We would like to thank Jane Cracknell, Managing Editor of the Cochrane Anaesthesia, Critical and Emergency Care Collaborative Review Group, for help and editorial advice provided during preparation of this update of the systematic review. We also acknowledge the efforts of Karen Hovhannisyan in assisting with the literature search .

We would like to thank Mathew Zacharias, Marialena Trivella, Ronan O’Sullivan, Stephen Priestley, Sujesh Bansal and Nete Villebro for their help and editorial advice in the past, Dr Joseph Lau for providing advice on statistics, and Dr Mukhtar Zaidi for providing pharmacological consultation.

Version history

Published

Title

Stage

Authors

Version

2017 Feb 22

Topical anaesthetics for pain control during repair of dermal laceration

Review

Baraa O Tayeb, Anthony Eidelman, Cristy L Eidelman, Ewan D McNicol, Daniel B Carr

https://doi.org/10.1002/14651858.CD005364.pub3

2011 Jun 15

Topical anaesthetics for pain control during repair of dermal laceration

Review

Baraa O Tayeb, Anthony Eidelman, Cristy L Eidelman, Ewan D McNicol, Daniel B Carr

https://doi.org/10.1002/14651858.CD005364.pub2

2005 Jul 20

Topical anaesthetics for repair of dermal laceration

Protocol

Anthony Eidelman, Jocelyn Weiss, Ikay K Enu, Joseph Lau, Ewan D McNicol, Daniel B Carr

https://doi.org/10.1002/14651858.CD005364

Differences between protocol and review

We made the following changes to the published protocol (Eidelman 2005a).

  1. We have changed the title from "Topical anaesthetics for repair of torn skin" to "Topical anaesthetics for pain control during repair of dermal laceration" for clarity.

  2. The name of co‐review author Cristy L Baldwin has been changed to Cristy L Eidelman.

  3. We have rephrased review objectives for clarity and simplification.

  4. We have rephrased review outcomes for clarity and simplification.

  5. We have updated methods and data collection on the basis of updated Cochrane standards.

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.

Flow diagram.
Figuras y tablas -
Figure 1

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.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 3

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Comparison 1 Topical prilocaine‐phenylephrine (PP) versus topical tetracaine‐epinephrine‐cocaine (TAC), Outcome 1 Patient self‐reported VAS (0‐100 mm) pain scores.
Figuras y tablas -
Analysis 1.1

Comparison 1 Topical prilocaine‐phenylephrine (PP) versus topical tetracaine‐epinephrine‐cocaine (TAC), Outcome 1 Patient self‐reported VAS (0‐100 mm) pain scores.

Summary of findings for the main comparison. Primary outcome: topical local anaesthetics compared with infiltrated local anaesthetics or other topical agents for repair of dermal lacerations

Pain control using topical local anaesthetics compared with infiltrated local anaesthetics or other topical agents for pain control during repair of dermal lacerations

Patient or population: adults and paediatric patients with dermal laceration

Settings: any medical setting

Intervention: topical local anaesthetics for pain control during repair of dermal laceration

Comparison: infiltrated local anaesthetics or other topical agents for pain control during repair of dermal lacerations

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

(Infiltrated local anaesthetics or other topical agents)

(Topical local anaesthetics)

Pain intensity measures

Cocaine‐containing topical anaesthetics vs infiltrated local anaesthetics

See comment

See comment

Not estimable

1006
(6 studies)

⊕⊕⊝⊝
Lowa

Unable to mathematically combine results because of heterogeneity of outcome measures

Pain intensity measures

Comparisons between different cocaine‐containing topical anaesthetics

See comment

See comment

Not estimable

530
(4 studies)

⊕⊕⊝⊝
Lowb

Unable to mathematically combine results because each topical anaesthetic comparison was limited to a single study

Pain intensity measures

Cocaine‐free topical anaesthetics compared with infiltrated local anaesthetics

See comment

See comment

Not estimable

543
(6 studies)

⊕⊕⊝⊝
Lowc

Unable to mathematically combine results because of heterogeneity of outcome measures

Pain intensity measures

Cocaine‐fee topical anaesthetics compared with cocaine‐containing topical anaesthetics

See comment

See comment

Not estimable

1231
(11 studies)

⊕⊕⊝⊝
Lowd

Two of the 11 trials studied a common topical anaesthetic and could be mathematically combined.

Pain intensity measures

Comparisons between different cocaine‐free topical anaesthetics

See comment

See comment

Not estimable

656
(5 studies)

⊕⊕⊝⊝
Lowe

Trials could not be mathematically combined because each study compared a different cocaine‐free topical anaesthetic.

Anaesthetic‐related adverse effects

Study population

RR 0

(0 to 0)

1686
(11 studies)

1 per 1000

0 per 1000
(0 to 0)

Medium‐risk population

*The basis for the assumed risk (e.g. median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on 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.

aEach of the trials had high risk of bias in multiple domains or unclear risk of bias in three domains.

bTwo of the four trials had at least one domain that was at high risk of bias.

cTwo of the trials had unclear risk of bias in multiple domains, and the other two studies had high risk of bias in two domains.

dSix of the studies had high risk of bias for at least one domain, and the other five studies had unclear risk of bias for one or more domains.

eEach of the five trials had unclear risk of bias in one or more domains. However, no trials contained any domains that were clearly at high risk

Figuras y tablas -
Summary of findings for the main comparison. Primary outcome: topical local anaesthetics compared with infiltrated local anaesthetics or other topical agents for repair of dermal lacerations
Summary of findings 2. Primary outcome subanalysis: pain intensity measures of topical prilocaine‐phenylephrine (PP) and topical tetracaine‐epinephrine‐cocaine (TAC)

Primary outcome subanalysis: pain intensity measures of topical prilocaine‐phenylephrine (PP) and topical tetracaine‐epinephrine‐cocaine (TAC)

Patient or population: treatment repair of dermal laceration

Setting: any medical setting
Intervention: topical prilocaine‐phenylephrine (PP)
Comparison: topical tetracaine‐epinephrine‐cocaine (TAC)

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with topical tetracaine‐epinephrine‐cocaine (TAC)

Risk with topical prilocaine‐phenylephrine (PP)

Participant self‐reported VAS (0‐100 mm) pain scores

Mean participant self‐reported VAS (0‐100 mm) pain score was 0.

Mean participant self‐reported VAS (0‐100 mm) pain scores in the intervention group was 5.59.

240
(2 studies)

Lowa

5.59 (95% CI for effect estimate, 2.16 to 13.35)

*Risk in the intervention group (and its 95% confidence interval) is based on assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; OR: odds ratio; RR: risk ratio.

GRADE Working Group grades of evidence.
High quality: We are very confident that the true effect lies close to the estimate of effect.
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of effect but may be substantially different.
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of effect.
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

aEach of the trials had unclear risk of bias in one or more domains. However, no trials included any domains that were clearly at high risk.

Figuras y tablas -
Summary of findings 2. Primary outcome subanalysis: pain intensity measures of topical prilocaine‐phenylephrine (PP) and topical tetracaine‐epinephrine‐cocaine (TAC)
Table 1. Cocaine‐containing topical anaesthetics versus infiltrated local anaesthetics

Study

Anaesthetics

Participant self‐reported pain scores

Secondary outcome measures

Incidence of anaesthetic toxicity

Anderson 1990

Topical tetracaine‐epinephrine‐cocaine (TAC) vs infiltrated lidocaine

None

1) Adequate initial anaesthesia (TAC = 89% vs infiltrated local anaesthetic = 79%; P = non‐significant)
2) Physician compliance scale(1 = complete compliance to 4 = continuous resistance) (mean score ± SD: TAC = 1.25 ± 0.57 vs infiltrated local anaesthetic = 1.94 ± 1.12; P < 0.002)
3) Requirement for supplemental lidocaine infiltration (topical TAC = 18% vs infiltrated local anaesthetic = 23%; P = non‐significant)

Not reported

Hegenbarth 1990

Topical TAC vs infiltrated lidocaine

None

1) Adequate initial anaesthesia for facial and scalp lacerations (topical TAC = 81% vs infiltrated local anaesthetic = 87%; P = 0.005). Adequate initial anaesthesia for extremity and trunk wounds (topical TAC = 43% vs infiltrated local anaesthetic = 89%; P < 0.0001)

0/467

Pryor 1980

Topical TAC vs infiltrated lidocaine

None

1) Verbal rating of anaesthetic efficacy (complete: TAC = 84% vs infiltrated local anaesthetic = 88%; P = not reported)
2) Anaesthetic acceptability: Participants 17 years or younger preferred topical TAC (P < 0.005); results showed no differences between the 2 anaesthetic groups among participants older than 17 years of age

Not reported

Smith 1996

Topical TAC vs infiltrated lidocaine

Patient‐reported VAS (100 mm) pain scores (mean scores: topical TAC = 12.0 vs infiltrated local anaesthetic = 26.3; P = NS)

1) Observer‐reported VAS pain scores
2) Observer‐reported Likert pain scores
3) Oberver‐rated Restrained Infants and Children Disress Rating Scale
4). Suture technician‐rated anaesthetic effectiveness

Not reported

Smith 1997a

Topical TAC vs infiltrated lidocaine

None

1) Observer‐reported VAS pain scores (suture technicians, research assistants, videotape reviewers)

2) Observer‐reported Lickert (1‐7) pain scores (parents, suture technicians)

3) Requirement for supplemental lidocaine infiltration

(See Characteristics of included studies for data.)

Not reported

Kendall 1996

Topical (epinephrine‐cocaine) AC vs infiltrated lidocaine

The study pooled patient‐reported VAS and Wong‐Baker Faces pain scores (mean score: topical AC = 4.50 vs infiltrated local anaesthetic = 4.40; P = NS)

1) Physician‐rated VAS pain scores
2) Parent‐rated VAS scores
3) Parents' rating of overall acceptability of procedure

0/107

AC: epinephrine (adrenaline) and cocaine; BN: bupivacaine‐noradrenaline; BP: blood pressure; cm: centimetre; c/w:compared with; ED: emergency department; EMLA: Eutectic Mixture of Local Anesthetics (lidocaine and prilocaine); EN: etidocaine‐noradrenaline; LAT: lidocaine, epinephrine and tetracaine (same as LET); LE: lidocaine and epinephrine; LET: same as LAT; LG: local gel; LI: local infiltration; MAC: bupivacaine 0.5%, epinephrine 1:2000, cocaine 10.0%; mm: milli‐metre; MN: mepivacaine‐noradrenaline; PN: prilocaine‐noradrenaline; N: number; NS: not significant; P = P value; PP: prilocaine, phenylephrine; RCT: randomized controlled trial; RICDRS: Restrained Infants and Children Distress Rating Scale; SD: standard deviation; SE: standard error; TA: tetracaine and epinephrine; TAC: tetracaine, epinephrine and cocaine; TLP: tetracaine, lidocaine and phenylephrine; TP: tetracaine and phenylephrine; VAS: visual analogue scale; vs: versus; w/w: weight per weight.

Figuras y tablas -
Table 1. Cocaine‐containing topical anaesthetics versus infiltrated local anaesthetics
Table 2. Comparisons between different cocaine‐containing topical anaesthetics

Study

Topical Anaesthetics

Patient self‐reported pain scores

Secondary outcome measures

Incidence anaesthetic toxicity

Kuhn 1996

Bupivacaine‐adrenaline‐cocaine (MAC) vs tetracaine‐epinephrine‐cocaine (TAC)

1) In children < 12 years of age: Wong‐Baker Faces (1‐9) Scale (mean score ± SD: topical MAC = 2.35 ± .50 vs topical TAC = 2.46 ± 2.34; P = 0.96)

2) Participants 12 years of age or older: VAS (100 mm) pain scale (mean score ± SD: topical MAC = 6.9 ± 10.9 vs topical TAC = 12.0 ± 14.5; P = 0.16)

1) Adequacy of initial anaesthesia

2) Participant preference for topical anaesthesia in the future

0/180

Bonadio 1990

TAC vs adrenaline‐cocaine (AC)

None

1) Physician calculated total number of 'sutures eliciting pain' (topical AC = 7/103 (4%) vs topical TAC = 7/151 (7%); P = not reported)

0/55

Ernst 1990

TAC vs cocaine (C)

None

1) Incidence of 'poor anaesthesia' (topical cocaine = 20% vs topical TAC = 12%; P = not reported)

2) Physician numerical rating of anaesthetic effectiveness (0 = least effective to 10 = most effective) (mean scores ± SD: topical cocaine = 6.44 ± 3.48 vs topical TAC = 7.74 ± 3.03; P = 0.005)

0/139

Vinci 1996

TAC (two different strengths) vs tetracaine‐cocaine (TC)

None

Topical TAC 1 vs topical TC:
1) Complete anaesthesia (TAC 1 = 73% vs TC = 28%; P < 0.001)

2) Requirement for second dose of topical anaesthetic (TAC 1 = 30% vs topical TC = 66%; P < 0.003)

3) Requirement for supplemental lidocaine infiltration (TAC 1 = 6% vs topical TC = 9%; P = not reported)

Topical TAC 2 vs topical TC:
1) Complete anaesthesia (TAC 2 = 63% vs TC = 28%; P < 0.001)

2) Requirement for second dose of topical anaesthetic (TAC 2 = 46% vs TC = 66%; P < 0.003)

3) Requirement for supplemental lidocaine infiltration (TAC 2 = 2% vs TC = 9%; P = not reported)

1/156 (erythematous rash 1 day after application of standard topical TAC)

Figuras y tablas -
Table 2. Comparisons between different cocaine‐containing topical anaesthetics
Table 3. Cocaine‐free topical anaesthetics versus infiltrated local anaesthetics

Study

Anaesthetics

Participant self‐reported pain scores

Secondary outcome measures

Incidence of anaesthetic toxicity

Ernst 1997

Topical lidocaine‐epinephrine‐tetracaine (LAT) vs infiltrated lidocaine

VAS (100 mm) pain scores (median values: topical LAT = 0 vs infiltrated local anaesthetic = 0; P = 0.48)

1) Physician‐rated VAS pain scores

2) Requirement for supplemental lidocaine infiltration

3) Percentage of painful sutures

Not reported

Gaufberg 2007

Topical lidocaine‐epinephrine (LE) vs infiltrated lidocaine

VAS (100 mm) pain scores (mean score ± SD: topical TLE = 0.16 ± 0.46 vs infiltrated lidocaine = 0.20 ± 0.49; P = 0.59)

1) Amount of lidocaine required (mg)

2) Total number of topical anaesthetic applications

Not reported

Smith 1996

Topical bupivacaine‐norepinephrine (BN), topical etidocaine‐norepinephrine (EN), topical mepivacaine‐norepinephrine (MN) and topical prilocaine‐norepinephrine (PN) vs infiltrated lidocaine

VAS (100 mm) pain scores (mean scores: BN = 18.3, EN = 46.5, MN = 27.0, PN = 36.0 vs infiltrated anaesthetic = 26.3, standard deviations not reported)

(no significant difference between any of the cocaine‐free topical agents and infiltrated lidocaine)

1) Observer‐reported VAS pain scores

2) Observer‐reported Likert pain scores

3) Oberver‐rated Restrained Infants and Children Disress Rating Scale

4) Suture technician‐rated anaesthetic effectiveness

Not reported

Smith 1997a

Topical mepivacaine‐norepinephrine (MN) vs infiltrated lidocaine

None

1) Observer‐reported VAS pain scale scores

2) Observer‐reported Lickert pain scores

3) Requirement for supplemental lidocaine infiltration

(See characteristics of included studies for data)

Not reported

Jenkins 2014

Topical anaesthetic putty (containing 4.94% w/w lidocaine hydrochloride, equivalent to 4% w/w lidocaine base) vs lidocaine infiltration (1% w/v)

Mean pain score was 0.78 + 1.12 (SD) after lidocaine infiltration, 1.49 + 1.76 after topical anaesthetic putty.

1) Need for rescue anaesthesia

2) Wound evaluation score 7‐10 days after treatment

3) Wound infection

4) Wound dehiscence

5) Adverse effects (inflamed wound or resuturing).

No anaesthetic toxicity reported

Lee 2013

Topical anaesthetic lidocaine, adrenaline and tetracaine (LAT) (4% lidocaine, 1:2 000 adrenaline, 1% tetracaine) vs lidocaine infiltration. Dosage of neither group was reported.

LAT gel group reported mean (± SE) pain intensity of 2.5 (0.52) vs 2.6 (0.58) for the lidocaine infiltration group. Pain during LAT application was 1.5 (0.40) vs 2.6 (0.58) during lidocaine infiltration (P ≤ 0.01).

1) Pain score by parents or clinicians (intended to be gathered for children < 10 years old but such data were not reported)

2) Wound complications

(infection, dehiscence,

missing sutures)

None reported

AC: epinephrine (adrenaline) and cocaine; BN: bupivacaine‐noradrenaline; BP: blood pressure; cm: centimetre; c/w: compared with; ED: emergency department; EMLA: Eutectic Mixture of Local Anesthetics (lidocaine and prilocaine); EN: etidocaine‐noradrenaline; LAT: lidocaine, epinephrine and tetracaine (same as LET); LE: lidocaine and epinephrine; LET: same as LAT; LG: local gel; LI: local infiltration; MAC: bupivacaine 0.5%, epinephrine 1:2000, cocaine 10.0%; mm: milli‐metre; MN: mepivacaine‐noradrenaline; PN: prilocaine‐noradrenaline; N: number; NS: not significant; P = P value; PP: prilocaine, phenylephrine; RCT: randomized controlled trial; RICDRS: Restrained Infants and Children Distress Rating Scale; SD: standard deviation; SE: standard error; TA: tetracaine and epinephrine; TAC: tetracaine, epinephrine and cocaine; TLP: tetracaine, lidocaine and phenylephrine; TP: tetracaine and phenylephrine; VAS: visual analogue scale; vs: versus; w/w: weight per weight.

Figuras y tablas -
Table 3. Cocaine‐free topical anaesthetics versus infiltrated local anaesthetics
Table 4. Cocaine‐free topical anaesthetics versus cocaine‐containing topical anaesthetics

Study

Topical anaesthetics

Participant self‐reported pain scores

Secondary outcome measures

Incidence of anaesthetic toxicity

Smith 1996

Bupivacaine‐norepinephrine (BN), etidocaine‐norepinephrine (EN), mepivacaine‐norepinephrine (MN) and prilocaine‐norepinephrine (PN) vs tetracaine‐epinephrine‐cocaine (TAC)

Participant‐reported VAS (100 mm) pain scores (mean scores: BN = 18.3, EN = 46.5, MN, PN = 36.0 vs TAC = 12.0, standard deviations not reported)

(TAC significantly outperformed EN; no significant differences between any other groups)

1) Observer‐reported VAS and Likert pain scale scores

2) Observer‐rated Restrained Infants and Children Disress Rating Scale

3) Suture technician‐rated anaesthetic effectiveness

Not reported

Smith 1997a

Mepivacaine‐norepinephrine (MN) vs
TAC

None

1) Observer‐reported VAS pain scores (suture technicians, research assistants, videotape reviewers)

2) Observer‐reported Lickert (1‐7) pain scores (parents, suture technicians)

3) Requirement for supplemental lidocaine infiltration

(See Characteristics of included studies for data.)

Not reported

Smith 1997b

Prilocaine‐phenylephrine (PP),
tetracaine‐phenylephrine (TP) and
tetracaine‐lidocaine‐phenylephrine (TLP) vs TAC

VAS (100 mm) pain scores (mean score ± SD: PP = 29.0 ± 43.4, TP = 24.2 ± 37.2, TLP = 30.6 ± 40.3 vs TAC = 17.6 ± 34.1 (no significant differences between groups; P = 0.5)

1) Oberver‐reported VAS (100 mm) pain scores

2) Oberver‐reported Likert (1‐7) pain scores

3) Suture technicians‐rated anaesthetic effectiveness

Not reported

Smith 1998a

Prilocaine‐phenylephrine (PP) and bupivacaine‐phenylephrine (BP) vs TAC

VAS (100 mm) pain scores (mean score ± SD: PP = 21.0 ± 28.0 and BP = 41.0 ± 35.0 vs TAC = 18.0 ± 24.0) (no differences reported between groups; P = 0.07)

Observer‐reported VAS pain scores (suture technicians, research assistants and parents)

Not reported

Ernst 1995a

LAT vs TAC

Modified multi‐dimensional pain scale (0‐10) (mean ranked sum: LAT = 49.0 vs TAC = 46.9; P = 0.71)

1) Physician‐rated modified multi‐dimensional pain scale (0‐10)

2) Percentage of sutures causing pain

3) Requirement for supplemental lidocaine infiltration

0/95

Ernst 1995b

LAT vs TAC

VAS (100 mm) pain scores (mean ranked sum: LET = 45.3 vs TAC = 50.8; P = 0.27)

1) Physician‐reported VAS scores

2) Percentage of sutures causing pain

Not reported

Schilling 1995

LAT vs TAC

None

1) Adequacy of initial anaesthesia (LAT = 74.4% vs TAC = 79.5%; P = 0.46)

2) Anaesthetic effectiveness (complete anaesthesia: LAT = 82.4% vs topical TAC = 75.9%; P = 0.18)

0/151

Zempsky 1997

Lidocaine‐prilocaine (EMLA) vs TAC

VAS (100 mm) pain scores (mean score ± SD: EMLA = 46.0 ± 26.0 vs TAC = 40.0 ± 25.0; P = 0.50)

1) Observer‐rated VAS pain scores

2) Requirement for supplemental lidocaine infiltration

Not reported

Blackburn 1995

Lidocaine‐epinephrine (LE) vs TAC

Faces pain scale (1‐9) scores (mean score ± SD: LE = 3.29 ± 1.92 vs TAC = 2.66 ± 1.78; P = 0.33)

Requirement for supplemental lidocaine infiltration

0/35

Schaffer 1985

Tetracaine‐epinephrine (TA) vs TAC

None

1) Physician‐rating of anaesthetic effectiveness (complete anaesthesia: TA = 47.1% vs TAC = 75%' P < 0.05)

2) Requirement for rescue lidocaine infiltration (TA = 27.5% vs TAC = 8.9%; P = 0.01)

0/107

White 1986

Tetracaine (T) vs TAC

Numerical pain scale (0‐10) score (mean scores: tetracaine = 5.6 vs TAC = 3.53; P < 0.05; standard deviations not reported)

Requirement for supplemental lidocaine infiltration

Not reported

AC: epinephrine (adrenaline) and cocaine; BN: bupivacaine‐noradrenaline; BP: blood pressure; cm: centimetre; c/w: compared with; ED: emergency department; EMLA: Eutectic Mixture of Local Anesthetics (lidocaine and prilocaine); EN: etidocaine‐noradrenaline; LAT: lidocaine, epinephrine and tetracaine (same as LET); LE: lidocaine and epinephrine; LET: same as LAT; LG: local gel; LI: local infiltration; MAC: bupivacaine 0.5%, epinephrine 1:2000, cocaine 10.0%; mm: milli‐metre; MN: mepivacaine‐noradrenaline; PN: prilocaine‐noradrenaline; N: number; NS: not significant; P = P value; PP: prilocaine, phenylephrine; RCT: randomized controlled trial; RICDRS: Restrained Infants and Children Distress Rating Scale; SD: standard deviation; SE: standard error; TA: tetracaine and epinephrine; TAC: tetracaine, epinephrine and cocaine; TLP: tetracaine, lidocaine and phenylephrine; TP: tetracaine and phenylephrine; VAS: visual analogue scale; vs: versus; w/w: weight per weight

Figuras y tablas -
Table 4. Cocaine‐free topical anaesthetics versus cocaine‐containing topical anaesthetics
Table 5. Comparisons between different cocaine‐free topical anaesthetics

Study

Topical anaesthetics

Participant self‐reported pain scores

Secondary outcome measures

Incidence of anaesthetic toxicity

Smith 1996

Bupivacaine‐norepinephrine (BN) vs etidocaine‐norepinephrine (EN) vs mepivacaine‐norepinephrine (MN) vs prilocaine‐norepinephrine (PN)

Patient‐reported VAS (100 mm) pain scores (mean scores: topical BN = 18.3 vs topical EN = 46.5 vs topical MN = 27.0 vs topical PN = 36.0) (no significant differences between any cocaine‐free topical groups)

1) Observer‐reported VAS and Likert pain scale scores

2) Observer‐rated Restrained Infants and Children Disress Rating Scale

3) Suture technician‐rated anaesthetic effectiveness

Not reported

Smith 1997b

Prilocaine‐phenylephrine (PP) vs
tetracaine‐phenylephrine (TP) vs
tetracaine‐lidocaine‐phenylephrine (TLP)

VAS (100 mm) pain scores (mean score ± SD: PP = 29.0 ± 43.4 vs TP = 24.2 ± 37.2 vs TLP = 30.6 ± 40.3) (no significant differences between groups; P = 0.5)

1) Oberver‐reported VAS (100 mm) pain scores

2) Oberver‐reported Likert (1‐7) pain scores

3) Suture technicians rated anaesthetic effectiveness

Not reported

Smith 1998a

Prilocaine‐phenylephrine (PP) vs bupivacaine‐phenylephrine (BP)

VAS (100 mm) pain scores (mean score ± SD: topical PP = 21.0 ± 28.0 vs topical BP = 41.0 ± 35.0; P = 0.07)

Observer‐reported VAS pain scores (suture technicians, research assistants and parents)

Not reported

Krief 2002

Lidocaine‐prilocaine (EMLA) vs lidocaine‐epinephrine‐tetracaine (LAT)

VAS (100 mm) pain scores were not significantly different between the 2 groups (mean pain scores not provided; P > 0.05).

1) Observer‐reported VAS pain scores (legal guardian and physician)

2) Requirement for supplemental lidocaine infiltration

Not reported

Resch 1998

Topical LAT gel vs LAT solution

None

1) Adequacy of initial anaesthesia (adequate anaesthesia: LAT solution = 84% vs LAT gel = 82%; P > 0.05)

2) Effectiveness of anaesthesia (complete anaesthesia: LAT solution = 76% vs LAT gel = 85%; P = 0.007)

0/194

AC: epinephrine (adrenaline) and cocaine; BN: bupivacaine‐noradrenaline; BP: blood pressure; cm: centimetre; c/w: compared with; ED: emergency department; EMLA: Eutectic Mixture of Local Anesthetics (lidocaine and prilocaine); EN: etidocaine‐noradrenaline; LAT: lidocaine, epinephrine and tetracaine (same as LET); LE: lidocaine and epinephrine; LET: same as LAT; LG: local gel; LI: local infiltration; MAC: bupivacaine 0.5%, epinephrine 1:2000, cocaine 10.0%; mm: milli‐metre; MN: mepivacaine‐noradrenaline; PN: prilocaine‐noradrenaline; N: number; NS: not significant; P = P value; PP: prilocaine, phenylephrine; RCT: randomized controlled trial; RICDRS: Restrained Infants and Children Distress Rating Scale; SD: standard deviation; SE: standard error; TA: tetracaine and epinephrine; TAC: tetracaine, epinephrine and cocaine; TLP: tetracaine, lidocaine and phenylephrine; TP: tetracaine and phenylephrine; VAS: visual analogue scale; vs: versus; w/w: weight per weight

Figuras y tablas -
Table 5. Comparisons between different cocaine‐free topical anaesthetics
Comparison 1. Topical prilocaine‐phenylephrine (PP) versus topical tetracaine‐epinephrine‐cocaine (TAC)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Patient self‐reported VAS (0‐100 mm) pain scores Show forest plot

2

240

Mean Difference (IV, Random, 95% CI)

5.59 [‐2.16, 13.35]

Figuras y tablas -
Comparison 1. Topical prilocaine‐phenylephrine (PP) versus topical tetracaine‐epinephrine‐cocaine (TAC)