Systematic review of the guidelines for retinopathy of prematurity

Author:

Kościółek Michał123ORCID,Kisielewska Weronika34ORCID,Ćwiklik-Wierzbowska Marlena5ORCID,Wierzbowski Piotr6ORCID,Gilbert Clare7

Affiliation:

1. University Clinical Center of the Medical University of Warsaw Central Clinical Hospital, Warsaw, Poland

2. Warsaw Genomics, Warsaw, Poland

3. Students’ Scientific Group “Lens”, Department of Ophthalmology, Medical University of Warsaw, Warsaw, Poland

4. Faculty of Medicine, Medical University of Warsaw, Warsaw, Poland

5. Military Institute of Medicine, Warsaw, Poland

6. Department of Internal Medicine and Endocrinology, University Clinical Center of the Medical University of Warsaw Central Clinical Hospital, Warsaw, Poland

7. Department of Clinical Research, London School of Hygiene & Tropical Medicine, London, UK

Abstract

As the characteristics of preterm infants with retinopathy of prematurity (ROP) vary, depending on the quality of neonatal care they received, universal screening criteria for ROP are not possible. The purpose of this study was to compare ROP guidelines for those planning to develop guidelines, particularly in resource-poor settings. A systematic review was undertaken of PubMed, Embase and guidelines registers to identify national or international policy statements or guidelines in English, issued or operational in 2010–2021. Bibliographies of two publications were also reviewed. The searches identified 633, 1081 and 317 records, respectively, and 157 records were retrieved from other sources. 23 publications were included in the analysis. Most included documents defined cut-offs for screening as <32 weeks gestational age (GA) or ≤1500g birth weight (BW). The highest values were in the Philippines (<35 weeks GA; <2000g) and India (≤34 weeks GA; <2000g). The lowest were in high-income countries, i.e. the United States of America (≤32 weeks for GA) and New Zealand (<1250g for BW). Most guidelines included additional risk factors to consider. The most frequent indication for when screening should start was a combination of GA and chronological age. All but one document defined when screening could stop. There was general consensus on the indications, timing and methods of treatment. Indications for anti-VEGF therapy varied between countries. Guidelines were identified for a limited number of countries with none from low-income settings. Variation in the indications for screening reflects the varying exposure to risk factors in different settings.

Publisher

SAGE Publications

Subject

Ophthalmology,General Medicine

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