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Cochrane Database of Systematic Reviews

Strategies for identifying familial hypercholesterolaemia in non‐specialist clinical settings

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Information

DOI:
https://doi.org/10.1002/14651858.CD012985Copy DOI
Database:
  1. Cochrane Database of Systematic Reviews
Version published:
  1. 20 March 2018see what's new
Type:
  1. Intervention
Stage:
  1. Protocol
Cochrane Editorial Group:
  1. Cochrane Cystic Fibrosis and Genetic Disorders Group

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

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Authors

  • Nadeem Qureshi

    Division of Primary Care, School of Medicine, University of Nottingham, Nottingham, UK

  • Stephen F Weng

    Division of Primary Care, School of Medicine, University of Nottingham, Nottingham, UK

  • Jennifer A Tranter

    Correspondence to: Division of Primary Care, University of Nottingham, Nottingham, UK

    [email protected]

  • Maria L Da Silva

    Division of Primary Care, University of Nottingham, Nottingham, UK

  • Joe Kai

    Division of Primary Care, School of Medicine, University of Nottingham, Nottingham, UK

  • Jo Leonardi‐Bee

    Division of Epidemiology and Public Health, The University of Nottingham, Nottingham, UK

Contributions of authors

Roles and Responsibilities

Protocol stage: (draft the protocol): NQ, JK, SW, J LB, JT, MD

Review stage: (select studies for inclusion): NQ, JT, MD, J LB

Review stage: (data extraction): SW, JT, MD, J LB

Review stage: JT, MD (contact authors for additional information)

Review stage: (enter data into ReVMan) JT, SW

Review stage: (carry out analysis) NQ, SW, J LB

Review stage: (interpretation of data) NQ, SW, JK, J LB

Review stage: (writing the final review) NQ, JK, SW, J LB, JT, MD

Update stage: (update the review) NQ, SW, JT

Sources of support

Internal sources

  • No sources of support supplied

External sources

  • National Institute for Health Research, UK.

    This systematic review was supported by the National Institute for Health Research, via Cochrane Infrastructure funding to the Cochrane Cystic Fibrosis and Genetic Disorders Group.

  • Nottingham City Clinical Commissioning Group, UK.

Declarations of interest

All authors: none known.

Acknowledgements

The authors would like to thank the Nottingham City Clinical Commissioning Group for commissioning and funding this review as part of a programme grant development award. The authors would also like to thank Dr Christopher Respinger for his contribution to the drafting of the section of the review: why it is important to do this review.

This project was supported by the National Institute for Health Research, via Cochrane Infrastructure funding to the Cochrane Cystic Fibrosis and Genetic Disorders Group. The views and opinions expressed therein are those of the authors and do not necessarily reflect those of the Systematic Reviews Programme, NIHR, NHS or the Department of Health.

Version history

Published

Title

Stage

Authors

Version

2021 Oct 07

Strategies for screening for familial hypercholesterolaemia in primary care and other community settings

Review

Nadeem Qureshi, Maria Luisa R Da Silva, Hasidah Abdul-Hamid, Stephen F Weng, Joe Kai, Jo Leonardi-Bee

https://doi.org/10.1002/14651858.CD012985.pub2

2018 Mar 20

Strategies for identifying familial hypercholesterolaemia in non‐specialist clinical settings

Protocol

Nadeem Qureshi, Stephen F Weng, Jennifer A Tranter, Maria L Da Silva, Joe Kai, Jo Leonardi‐Bee

https://doi.org/10.1002/14651858.CD012985

Keywords

MeSH

Medical Subject Headings Check Words

Humans;

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.