Evidence map›Paper›PMID 35350161›Full record

ArticleThe journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG2022

Using A Work System Framework to Investigate Pharmacists' Roles in Cystic Fibrosis Management.

Olufunmilola Abraham, Megan Buechel, Sommer Gay, Lisa Szela, Catherine A Decker, Andrew T Braun

Open access · greenAbstract read
In one paragraph

Article in The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

6 authors at 1 institution in 1 country.

Olufunmilola AbrahamUniversity of Wisconsin-Madison School of Pharmacy, Social and Administrative Sciences Division (OA, MB, SG, LS), Madison, WI.
Megan BuechelUniversity of Wisconsin-Madison School of Pharmacy, Social and Administrative Sciences Division (OA, MB, SG, LS), Madison, WI.
Sommer GayUniversity of Wisconsin-Madison School of Pharmacy, Social and Administrative Sciences Division (OA, MB, SG, LS), Madison, WI.
Lisa SzelaUniversity of Wisconsin-Madison School of Pharmacy, Social and Administrative Sciences Division (OA, MB, SG, LS), Madison, WI.
Catherine A DeckerSchool of Medicine and Public Health, University of Wisconsin-Madison (ATB, CAD), Madison, WI.
Andrew T BraunSchool of Medicine and Public Health, University of Wisconsin-Madison (ATB, CAD), Madison, WI.
University of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCystic fibrosis (CF) is a genetic disease that requires complex, lifelong treatment regimens to maintain health and reduce disease progression. The aims of this study were 1) to gain the perspectives of multiple health professions to understand medication and well-being challenges of people living with CF; and 2) to apply the Systems Engineering Initiative for Patient Safety (SEIPS) model to further identify opportunities for pharmacists to support people with CF.

methodsHealth care professionals were recruited from a Cystic Fibrosis Center in the Midwest, to participate in audio-recorded semistructured interviews. Topics examined during the interviews included medication education for patients as well as experiences with outpatient, specialty, and community pharmacists. The themes assessed during the pharmacist interviews included support for people living with CF, preferences in conducting medication education, and pharmacist-specific counseling. Interview transcripts were thematically analyzed into categories to determine major themes. Prevalent codes were categorized into 5 major themes guided by the SEIPS model. Interrater reliability was strong (kappa = 0.94).

resultsFive major themes were identified: 1) patient tasks; 2) external environment; 3) organizational conditions; 4) patient medication education; and 5) pharmacists' roles and tasks. Professionals identified the importance of the pharmacist on the multidisciplinary CF care team to enhance patient-centered care for people living with CF.

conclusionsThis study highlights health care professionals' views on the unique skillset that pharmacists add to the care team, including a reduction in medication errors, improved adherence, and overall enhanced patient care.

Indexed as

cystic fibrosismultidisciplinary care teampharmacistSEIPS model

Identifiers

PMID35350161
PMCPMC8939272
OpenAlexW4226174472

What OpenQuestion holds

Textmetadata
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.