Healthcare providers' use of a concise summary to prescribe for lactating patients.

Breastfeeding Pregnancy and lactation labeling rule Prescribing information Prescribing/counseling decision making Prescription drug labeling Risk communication

Journal

Research in social & administrative pharmacy : RSAP
ISSN: 1934-8150
Titre abrégé: Res Social Adm Pharm
Pays: United States
ID NLM: 101231974

Informations de publication

Date de publication:
19 Feb 2024
Historique:
received: 18 12 2023
revised: 07 02 2024
accepted: 10 02 2024
medline: 28 2 2024
pubmed: 28 2 2024
entrez: 27 2 2024
Statut: aheadofprint

Résumé

Most breastfeeding individuals take at least one prescription drug, yet limited data from lactation studies are available to inform the safety of these drugs during breastfeeding. As a result, healthcare providers (HCPs) rely on available information about safety of drugs used during pregnancy or on personal experiences to inform prescribing/counseling decisions for breastfeeding individuals. To improve risk communication regarding drugs used during lactation, the U.S. Food and Drug Administration published the Pregnancy and Lactation Labeling Rule (PLLR) in 2015, which added a narrative summary of available risk information to the lactation section of Prescribing Information (PI). Prior studies on labeling in PLLR format revealed that although HCPs found these details valuable, they regarded the narrative as too long to support decision-making during patient encounters. This qualitative study's objective was to assess the utility of adding a concise summary to the Lactation subsection of PI to complement the narrative and succinctly communicate to busy HCPs a drug's risks when used during lactation. The concise summary consisted of a bolded headline, bulleted descriptions of available study findings and potential adverse reactions, and recommendations for risk mitigation. Twenty-five online focus groups were conducted with five segments of HCPs to obtain their feedback on the concise summary and discuss their prescribing/counseling decisions for four fictitious prescription drugs including one vaccine. HCPs utilized the concise summary to make initial prescribing/counseling decisions. Many also used the labeling narrative for a comprehensive benefit-risk assessment. The findings indicate a need to continue to improve communication about safety of drugs used during lactation, and that the concise summary may help facilitate this communication. The study also highlights the need to educate HCPs about PI limitations when clinical data are lacking and the need to encourage clinical studies to be conducted to support actionable recommendations about use of prescription drugs during lactation.

Sections du résumé

BACKGROUND BACKGROUND
Most breastfeeding individuals take at least one prescription drug, yet limited data from lactation studies are available to inform the safety of these drugs during breastfeeding. As a result, healthcare providers (HCPs) rely on available information about safety of drugs used during pregnancy or on personal experiences to inform prescribing/counseling decisions for breastfeeding individuals. To improve risk communication regarding drugs used during lactation, the U.S. Food and Drug Administration published the Pregnancy and Lactation Labeling Rule (PLLR) in 2015, which added a narrative summary of available risk information to the lactation section of Prescribing Information (PI). Prior studies on labeling in PLLR format revealed that although HCPs found these details valuable, they regarded the narrative as too long to support decision-making during patient encounters.
OBJECTIVE OBJECTIVE
This qualitative study's objective was to assess the utility of adding a concise summary to the Lactation subsection of PI to complement the narrative and succinctly communicate to busy HCPs a drug's risks when used during lactation. The concise summary consisted of a bolded headline, bulleted descriptions of available study findings and potential adverse reactions, and recommendations for risk mitigation.
METHODS METHODS
Twenty-five online focus groups were conducted with five segments of HCPs to obtain their feedback on the concise summary and discuss their prescribing/counseling decisions for four fictitious prescription drugs including one vaccine.
RESULTS RESULTS
HCPs utilized the concise summary to make initial prescribing/counseling decisions. Many also used the labeling narrative for a comprehensive benefit-risk assessment.
CONCLUSION CONCLUSIONS
The findings indicate a need to continue to improve communication about safety of drugs used during lactation, and that the concise summary may help facilitate this communication. The study also highlights the need to educate HCPs about PI limitations when clinical data are lacking and the need to encourage clinical studies to be conducted to support actionable recommendations about use of prescription drugs during lactation.

Identifiants

pubmed: 38413289
pii: S1551-7411(24)00051-2
doi: 10.1016/j.sapharm.2024.02.004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Published by Elsevier Inc.

Auteurs

Teresa Koenig (T)

Westat, United States.

Cynthia Robins (C)

Westat, United States.

Paula Darby Lipman (P)

Westat, United States.

Miriam Dinatale (M)

United States Food and Drug Administration, United States. Electronic address: miriam.dinatale@fda.hhs.gov.

Tamara Johnson (T)

United States Food and Drug Administration, United States.

Leyla Sahin (L)

United States Food and Drug Administration, United States.

Catherine Roca (C)

United States Food and Drug Administration, United States.

Jeannie Limpert (J)

United States Food and Drug Administration, United States.

Kristie Baisden (K)

United States Food and Drug Administration, United States.

Yeruk Mulugeta (Y)

United States Food and Drug Administration, United States.

Lynne Yao (L)

United States Food and Drug Administration, United States.

Kerri-Ann Jennings (KA)

United States Food and Drug Administration, United States.

Meghna Alimchandani (M)

United States Food and Drug Administration, United States.

Darcie Everett (D)

United States Food and Drug Administration, United States.

Audrey Gassman (A)

United States Food and Drug Administration, United States.

Christina Chang (C)

United States Food and Drug Administration, United States.

Christopher Ellis (C)

United States Food and Drug Administration, United States.

Elimika Pfuma Fletcher (E)

United States Food and Drug Administration, United States.

Sherbet Samuels (S)

United States Food and Drug Administration, United States.

Classifications MeSH