TY - JOUR
T1 - A Participatory Framework for Plain Language Clinical Management Guideline Development
AU - Francisco, Rita
AU - Alves, Susana
AU - Gomes, Catarina
AU - Granjo, Pedro
AU - Pascoal, Carlota
AU - Brasil, Sandra
AU - Neves, Alice
AU - Santos, Inês
AU - Miller, Andrea
AU - Krasnewich, Donna
AU - Morava, Eva
AU - Lam, Christina
AU - Jaeken, Jaak
AU - Videira, Paula A.
AU - dos Reis Ferreira, Vanessa
N1 - Funding Information:
info:eu-repo/grantAgreement/FCT/OE/SFRH%2FBD%2F124326%2F2016/PT#
info:eu-repo/grantAgreement/FCT/OE/SFRH%2FBD%2F138647%2F2018/PT#
Sandra Brasil was supported by CDG & Allies—PPAIN funding.
Publisher Copyright:
© 2022 by the authors.
PY - 2022/10/19
Y1 - 2022/10/19
N2 - Background: Clinical management guidelines (CMGs) are decision support tools for patient care used by professionals, patients, and family caregivers. Since clinical experts develop numerous CMGs, their technical language hinders comprehension and access by nonmedical stakeholders. Additionally, the views of affected individuals and their families are often not incorporated into treatment guidelines. We developed an adequate methodology for addressing the needs and preferences of family and professional stakeholders regarding CMGs, a recently developed protocol for managing congenital disorders of glycosylation (CDG), a family of rare metabolic diseases. We used the CDG community and phosphomannomutase 2 (PMM2)-CDG CMGs as a pilot to test and implement our methodology. Results: We listened to 89 PMM2-CDG families and 35 professional stakeholders and quantified their CMG-related needs and preferences through an electronic questionnaire. Most families and professionals rated CMGs as relevant (86.5% and 94.3%, respectively), and valuable (84.3% and 94.3%, respectively) in CDG management. The most identified challenges were the lack of CMG awareness (50.6% of families) and the lack of plain language CMG (39.3% of professionals). Concordantly, among families, the most suggested solution was involving them in CMG development (55.1%), while professionals proposed adapting CMGs to include plain language (71.4%). Based on these results, a participatory framework built upon health literacy principles was created to improve CMG comprehension and accessibility. The outputs are six complementary CMG-related resources differentially adapted to the CDG community’s needs and preferences, with a plain language PMM2-CDG CMG as the primary outcome. Additionally, the participants established a distribution plan to ensure wider access to all resources. Conclusions: This empowering, people-centric methodology accelerates CMG development and accessibility to all stakeholders, ultimately improving the quality of life of individuals living with a specific condition and raising the possibility of application to other clinical guidelines.
AB - Background: Clinical management guidelines (CMGs) are decision support tools for patient care used by professionals, patients, and family caregivers. Since clinical experts develop numerous CMGs, their technical language hinders comprehension and access by nonmedical stakeholders. Additionally, the views of affected individuals and their families are often not incorporated into treatment guidelines. We developed an adequate methodology for addressing the needs and preferences of family and professional stakeholders regarding CMGs, a recently developed protocol for managing congenital disorders of glycosylation (CDG), a family of rare metabolic diseases. We used the CDG community and phosphomannomutase 2 (PMM2)-CDG CMGs as a pilot to test and implement our methodology. Results: We listened to 89 PMM2-CDG families and 35 professional stakeholders and quantified their CMG-related needs and preferences through an electronic questionnaire. Most families and professionals rated CMGs as relevant (86.5% and 94.3%, respectively), and valuable (84.3% and 94.3%, respectively) in CDG management. The most identified challenges were the lack of CMG awareness (50.6% of families) and the lack of plain language CMG (39.3% of professionals). Concordantly, among families, the most suggested solution was involving them in CMG development (55.1%), while professionals proposed adapting CMGs to include plain language (71.4%). Based on these results, a participatory framework built upon health literacy principles was created to improve CMG comprehension and accessibility. The outputs are six complementary CMG-related resources differentially adapted to the CDG community’s needs and preferences, with a plain language PMM2-CDG CMG as the primary outcome. Additionally, the participants established a distribution plan to ensure wider access to all resources. Conclusions: This empowering, people-centric methodology accelerates CMG development and accessibility to all stakeholders, ultimately improving the quality of life of individuals living with a specific condition and raising the possibility of application to other clinical guidelines.
KW - clinical management guidelines
KW - congenital disorders of glycosylation (CDG)
KW - health literacy
KW - participatory medicine
KW - people-centric
KW - plain language
KW - PMM2-CDG
KW - rare diseases
UR - http://www.scopus.com/inward/record.url?scp=85140907901&partnerID=8YFLogxK
U2 - 10.3390/ijerph192013506
DO - 10.3390/ijerph192013506
M3 - Article
C2 - 36294089
AN - SCOPUS:85140907901
SN - 1661-7827
VL - 19
JO - International Journal of Environmental Research and Public Health
JF - International Journal of Environmental Research and Public Health
IS - 20
M1 - 13506
ER -