Availability, scope and quality of monkeypox clinical management guidelines globally: a systematic review.


Journal

BMJ global health
ISSN: 2059-7908
Titre abrégé: BMJ Glob Health
Pays: England
ID NLM: 101685275

Informations de publication

Date de publication:
08 2022
Historique:
received: 08 06 2022
accepted: 07 07 2022
entrez: 16 8 2022
pubmed: 17 8 2022
medline: 19 8 2022
Statut: ppublish

Résumé

Monkeypox (MPX) is an important human Orthopoxvirus infection. There has been an increase in MPX cases and outbreaks in endemic and non-endemic regions in recent decades. We appraised the availability, scope, quality and inclusivity of clinical management guidelines for MPX globally. For this systematic review, we searched six databases from inception until 14 October 2021, augmented by a grey literature search until 17 May 2022. MPX guidelines providing treatment and supportive care recommendations were included, with no exclusions for language. Two reviewers assessed the guidelines. Quality was assessed using the Appraisal of Guidelines for Research and Evaluation II tool. Of 2026 records screened, 14 guidelines were included. Overall, most guidelines were of low-quality with a median score of 2 out of 7 (range: 1-7), lacked detail and covered a narrow range of topics. Most guidelines focused on adults, five (36%) provided some advice for children, three (21%) for pregnant women and three (21%) for people living with HIV. Treatment guidance was mostly limited to advice on antivirals; seven guidelines advised cidofovir (four specified for severe MPX only); 29% (4/14) tecovirimat, and 7% (1/14) brincidofovir. Only one guideline provided recommendations on supportive care and treatment of complications. All guidelines recommended vaccination as post-exposure prophylaxis (PEP). Three guidelines advised on vaccinia immune globulin as PEP for severe cases in people with immunosuppression. Our results highlight a lack of evidence-based clinical management guidelines for MPX globally. There is a clear and urgent need for research into treatment and prophylaxis including for different risk populations. The current outbreak provides an opportunity to accelerate this research through coordinated high-quality studies. New evidence should be incorporated into globally accessible guidelines, to benefit patient and epidemic outcomes. A 'living guideline' framework is recommended. CRD42020167361.

Sections du résumé

BACKGROUND
Monkeypox (MPX) is an important human Orthopoxvirus infection. There has been an increase in MPX cases and outbreaks in endemic and non-endemic regions in recent decades. We appraised the availability, scope, quality and inclusivity of clinical management guidelines for MPX globally.
METHODS
For this systematic review, we searched six databases from inception until 14 October 2021, augmented by a grey literature search until 17 May 2022. MPX guidelines providing treatment and supportive care recommendations were included, with no exclusions for language. Two reviewers assessed the guidelines. Quality was assessed using the Appraisal of Guidelines for Research and Evaluation II tool.
RESULTS
Of 2026 records screened, 14 guidelines were included. Overall, most guidelines were of low-quality with a median score of 2 out of 7 (range: 1-7), lacked detail and covered a narrow range of topics. Most guidelines focused on adults, five (36%) provided some advice for children, three (21%) for pregnant women and three (21%) for people living with HIV. Treatment guidance was mostly limited to advice on antivirals; seven guidelines advised cidofovir (four specified for severe MPX only); 29% (4/14) tecovirimat, and 7% (1/14) brincidofovir. Only one guideline provided recommendations on supportive care and treatment of complications. All guidelines recommended vaccination as post-exposure prophylaxis (PEP). Three guidelines advised on vaccinia immune globulin as PEP for severe cases in people with immunosuppression.
CONCLUSION
Our results highlight a lack of evidence-based clinical management guidelines for MPX globally. There is a clear and urgent need for research into treatment and prophylaxis including for different risk populations. The current outbreak provides an opportunity to accelerate this research through coordinated high-quality studies. New evidence should be incorporated into globally accessible guidelines, to benefit patient and epidemic outcomes. A 'living guideline' framework is recommended.
PROSPERO REGISTRATION NUMBER
CRD42020167361.

Identifiants

pubmed: 35973747
pii: bmjgh-2022-009838
doi: 10.1136/bmjgh-2022-009838
pmc: PMC9472169
pii:
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S019987/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T001151/1
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: PH is a senior research advisor and HG is a research manager at the Wellcome Trust, which provided part of the funding for this work, but neither had a role in data collection, analysis nor interpretation of the findings. The funders had a role in writing the report but do not stand to materially benefit from the work. Wellcome supports a range of research funding activities including awards made to International Severe Acute Respiratory and Emerging Infection Consortium.

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Auteurs

Eika Webb (E)

Liverpool School of Tropical Medicine, Liverpool, Liverpool, UK.

Ishmeala Rigby (I)

ISARIC Global Support Centre, Pandemic Sciences Institute, University of Oxford, Oxford, Oxfordshire, UK.

Melina Michelen (M)

ISARIC Global Support Centre, Pandemic Sciences Institute, University of Oxford, Oxford, Oxfordshire, UK.

Andrew Dagens (A)

ISARIC Global Support Centre, Pandemic Sciences Institute, University of Oxford, Oxford, Oxfordshire, UK.

Vincent Cheng (V)

Bristol Medical School, Unversity of Bristol, Bristol, UK.

Amanda M Rojek (AM)

ISARIC Global Support Centre, Pandemic Sciences Institute, University of Oxford, Oxford, Oxfordshire, UK.
Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Dania Dahmash (D)

ISARIC Global Support Centre, Pandemic Sciences Institute, University of Oxford, Oxford, Oxfordshire, UK.

Susan Khader (S)

GloPID-R, University of Oxford, Oxford, Oxfordshire, UK.

Keerti Gedela (K)

Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Alice Norton (A)

GloPID-R, University of Oxford, Oxford, Oxfordshire, UK.

Muge Cevik (M)

Divison of Infection and Global Health Research, School of Medicine, University of St. Andrews, St Andrews, UK.

Erhui Cai (E)

ISARIC Global Support Centre, Pandemic Sciences Institute, University of Oxford, Oxford, Oxfordshire, UK.

Eli Harriss (E)

Bodleian Health Care Libraries, University of Oxford, Oxford, UK.

Samuel Lipworth (S)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Robert Nartowski (R)

ISARIC Global Support Centre, Pandemic Sciences Institute, University of Oxford, Oxford, Oxfordshire, UK.

Helen Groves (H)

Wellcome Trust, London, London, UK.

Peter Hart (P)

Wellcome Trust, London, London, UK.

Lucille Blumberg (L)

National Institute for Communicable Diseases, Johannesburg, South Africa.

Tom Fletcher (T)

Liverpool School of Tropical Medicine, Liverpool, Liverpool, UK.

Shevin T Jacob (ST)

Liverpool School of Tropical Medicine, Liverpool, Liverpool, UK.

Louise Sigfrid (L)

ISARIC Global Support Centre, Pandemic Sciences Institute, University of Oxford, Oxford, Oxfordshire, UK louise.sigfrid@gmail.com.
GloPID-R, University of Oxford, Oxford, Oxfordshire, UK.

Peter W Horby (PW)

ISARIC Global Support Centre, Pandemic Sciences Institute, University of Oxford, Oxford, Oxfordshire, UK.

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