Guidelines or Other Guidance Documents for Rare Diseases in the Netherlands: When and Where to Invest (Effort, Time and Money)?

ABSTRACT Introduction Developing Clinical Practice Guidelines (CPGs) is resource‐intensive, making it essential to prioritise those CPG projects that are most needed. One of the rules pertains to prevalence, which excludes virtually all guideline development for rare diseases. Still, guidance is needed for their management. We discuss considerations pertaining to the decision to develop a CPG or another type of guidance document for a rare disease. Methods Using a consensus‐based approach, an expert group developed a decision support flowchart to decide about the development of a clinical practice guideline or an alternative type of guidance document for rare diseases. An expert group of three guideline methodologists, a paediatrician, and two quality of care policy officers drafted an initial flowchart. The flowchart was reviewed and refined through three rounds of steering committee discussions in different settings, after which final adaptations were made. Results The flowchart serves as a support tool to consider whether a CPG is the most suitable type of guidance document for addressing clinical challenges in a particular rare disease. Several alternatives may be more appropriate than developing a CPG, such as a local protocol, a care pathway, a didactic paper, or adolopment or adaptation of an international CPG illustrated by three conditions. Discussion The proposed flowchart provides a framework to consider all relevant aspects around the choice for development of a guidance document or CPG. Although it results from the Dutch national situation and the rare disease field, it may also be applied in other countries and for more prevalent diseases. We encourage external validation and, if necessary, refinement of the flowchart. It supports strategic decision‐making, ensuring that the efforts and resources needed for the development of CPGs or other guidance documents are focused on areas where they will have the greatest impact on medical specialist care.

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Publication Details

Journal
Clinical and Public Health Guidelines
Published
2026-05-12
DOI
https://doi.org/10.1002/gin2.70070
Primary Topic
Clinical practice guidelines implementation
Type
article
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article

Guidelines or Other Guidance Documents for Rare Diseases in the Netherlands: When and Where to Invest (Effort, Time and Money)?

Marieke Hermsen, Charlotte M.W. Gaasterland, Iméze J. Hieltjes, Ilse van Herk et al.
Clinical and Public Health Guidelines
Clinical practice guidelines implementation
article

Guidelines or Other Guidance Documents for Rare Diseases in the Netherlands: When and Where to Invest (Effort, Time and Money)?

Marieke Hermsen, Charlotte M.W. Gaasterland, Iméze J. Hieltjes, Ilse van Herk, Johanna H. van der Lee, Anne Marie van Wermeskerken
article en

Abstract

ABSTRACT Introduction Developing Clinical Practice Guidelines (CPGs) is resource‐intensive, making it essential to prioritise those CPG projects that are most needed. One of the rules pertains to prevalence, which excludes virtually all guideline development for rare diseases. Still, guidance is needed for their management. We discuss considerations pertaining to the decision to develop a CPG or another type of guidance document for a rare disease. Methods Using a consensus‐based approach, an expert group developed a decision support flowchart to decide about the development of a clinical practice guideline or an alternative type of guidance document for rare diseases. An expert group of three guideline methodologists, a paediatrician, and two quality of care policy officers drafted an initial flowchart. The flowchart was reviewed and refined through three rounds of steering committee discussions in different settings, after which final adaptations were made. Results The flowchart serves as a support tool to consider whether a CPG is the most suitable type of guidance document for addressing clinical challenges in a particular rare disease. Several alternatives may be more appropriate than developing a CPG, such as a local protocol, a care pathway, a didactic paper, or adolopment or adaptation of an international CPG illustrated by three conditions. Discussion The proposed flowchart provides a framework to consider all relevant aspects around the choice for development of a guidance document or CPG. Although it results from the Dutch national situation and the rare disease field, it may also be applied in other countries and for more prevalent diseases. We encourage external validation and, if necessary, refinement of the flowchart. It supports strategic decision‐making, ensuring that the efforts and resources needed for the development of CPGs or other guidance documents are focused on areas where they will have the greatest impact on medical specialist care.

Clinical and Public Health GuidelinesVol. 3(3)
Leiden University Medical Center (NL), Royal Dutch Pharmacists Association (NL), Emma Kinderziekenhuis (NL), Nederlandse Vereniging voor Kindergeneeskunde (NL), Flevoziekenhuis (NL), Dutch Hospital Association (NL)
Partnerships for the goals
Openalex Percentile: Top 5%
Clinical practice guidelines implementation
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