Evidence map›Paper›PMID 37640492›Full record

ArticleGlobal health, science and practice2023

Digitalizing Clinical Guidelines: Experiences in the Development of Clinical Decision Support Algorithms for Management of Childhood Illness in Resource-Constrained Settings.

Fenella Beynon, Frédérique Guérin, Riccardo Lampariello, Torsten Schmitz, Rainer Tan, Natschja Ratanaprayul, Tigest Tamrat, Karell G Pellé, Gaud Catho, Kristina Keitel and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Global health, science and practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
6.8field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 10 institutions in 4 countries.

Fenella BeynonSwiss Tropical and Public Health Institute, Basel, Switzerland.
Frédérique GuérinGeneva Science-Policy Interface, University of Geneva, Switzerland.
Riccardo LamparielloTerre des Hommes, Lausanne, Switzerland.
Torsten SchmitzSwiss Tropical and Public Health Institute, Basel, Switzerland.
Rainer TanSwiss Tropical and Public Health Institute, Basel, Switzerland.
Natschja RatanaprayulDepartment of Digital Health and Innovations, World Health Organization, Geneva, Switzerland.
Tigest TamratUNDP/UNFPA/UNICEF/World Bank Special Program of Research, Development and Research Training in Human Reproduction (HRP), Department of Sexual and Reproductive Health and Research, World Health Organization, Geneva, Switzerland.
Karell G PelléFIND, Geneva, Switzerland.
Gaud CathoDivision of Infectious Diseases, Geneva University Hospital and Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Kristina KeitelSwiss Tropical and Public Health Institute, Basel, Switzerland.
Irene MasanjaIfakara Health Institute, Dar es Salaam, Tanzania.
Clotilde Rambaud-AlthausMédecins Sans Frontières Switzerland, Operational Center Geneva, Geneva, Switzerland.
University of Basel · CHUniversity of Geneva · CHD-Tree International · USFIND · CHIfakara Health Institute · TZMédecins Sans Frontières · CHSwiss Tropical and Public Health Institute · CHUniversity Hospital of Bern · CHWorld Health Organization · CHWorld Health Organization - Pakistan · PK

Funding

World Health Organization 001
6 · The paper itself

Abstract

Clinical decision support systems (CDSSs) can strengthen the quality of integrated management of childhood illness (IMCI) in resource-constrained settings. Several IMCI-related CDSSs have been developed and implemented in recent years. Yet, despite having a shared starting point, the IMCI-related CDSSs are markedly varied due to the need for interpretation when translating narrative guidelines into decision logic combined with considerations of context and design choices. Between October 2019 and April 2021, we conducted a comparative analysis of 4 IMCI-related CDSSs. The extent of adaptations to IMCI varied, but common themes emerged. Scope was extended to cover a broader range of conditions. Content was added or modified to enhance precision, align with new evidence, and support rational resource use. Structure was modified to increase efficiency, improve usability, and prioritize care for severely ill children. The multistakeholder development processes involved syntheses of recommendations from existing guidelines and literature; creation and validation of clinical algorithms; and iterative development, implementation, and evaluation. The common themes surrounding adaptations of IMCI guidance highlight the complexities of digitalizing evidence-based recommendations and reinforce the rationale for leveraging standards for CDSS development, such as the World Health Organization's SMART Guidelines. Implementation through multistakeholder dialogue is critical to ensure CDSSs can effectively and equitably improve quality of care for children in resource-constrained settings.

Indexed as

Decision Support Systems, ClinicalIchthyosiform Erythroderma, CongenitalLipid Metabolism, Inborn ErrorsAlgorithmsChildHumans

Identifiers

PMID37640492
PMCPMC10461705
OpenAlexW4385356748

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.