Evidence map›Paper›PMID 24415776›Full record

ArticleBMJ quality & safety2014

Improving transition from paediatric to adult cystic fibrosis care: programme implementation and evaluation.

Megumi J Okumura, Thida Ong, Diana Dawson, Dennis Nielson, Nancy Lewis, Martha Richards, Claire D Brindis, Mary Ellen Kleinhenz

Abstract read
In one paragraph

Article in BMJ quality & safety, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Transition Care in Cystic Fibrosis.Indian journal of pediatrics · 2023
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Managing the transition from paediatric to adult care for HIV, Kenya.Bulletin of the World Health Organization · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cystic fibrosis.Nature reviews. Disease primers · 2015
    Review
  20. 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

8 authors.

Megumi J OkumuraDivision of General Pediatrics, University of California, , San Francisco, California, USA.
Thida Ong
Diana Dawson
Dennis Nielson
Nancy Lewis
Martha Richards
Claire D Brindis
Mary Ellen Kleinhenz

Funding

SynthesisP30DK072517 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CIL, ONUR · 2005 to 2022
$18.1M
Barriers & Facilitators to Health Care: Transitioning Youth with Special NeedsK08HS017716 · AHRQ · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI OKUMURA, MEGUMI J · 2008 to 2012
$683k
AHRQ HHS K08 HS017716AHRQ HHS K08HS017716-01NIDDK NIH HHS P30 DK072517
6 · The paper itself

Abstract

backgroundThe paradigm of cystic fibrosis (CF) care has changed as effective therapies extend the lives of patients well into adulthood. Preparing for and maintaining high quality CF care into the adult healthcare setting is critical for prolonged survival. Unfortunately, this transfer process from the paediatric to the adult CF centre is met with a variety of challenges. OBJECTIVE AND

methodsThe objective of this quality improvement (QI) project was to develop, implement and evaluate a theory-based programme for transition from paediatric to adult CF care. In a multi-phase process, the paediatric and adult programmes developed a transition curriculum, addressed care standards and standardised patient transfer protocols. We evaluated the impact of this process through staff surveys, review of field notes from QI meetings, tracking transfers and responses of patients to the Transition Readiness Assessment Questionnaire (TRAQ) at the start of the programme and 18 months after initiation.

resultsThe collaboration between the paediatric and adult teams continued through quarterly meetings over the past 4 years. This has provided a forum that sustained our transition programme, harmonised care across CF centres and addressed other needs of our CF centre. Discussion of transition with families in the paediatric centre increased twofold (35% to 73% p<0.001), and resulted in a trend towards improved patient TRAQ self-advocacy scores and decreased in-hospital transfer.

conclusionsWe successfully created a curriculum and process for transition from paediatric to adult CF care at our centres. This collaboration shapes the communication between our paediatric and adult CF care teams and enables ongoing feedback among patients, families and providers. The impact of our transition programme on long-term patient morbidity will require future evaluation.

Indexed as

Quality of Health CareAdolescentAdultChildChild, PreschoolCystic FibrosisHumansPatient CarePatient Care TeamProgram DevelopmentProgram EvaluationQuality ImprovementTransition to Adult CareUnited StatesYoung AdultPatient EducationQuality ImprovementTransitions in Care

Identifiers

PMID24415776
PMCPMC4449274

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Registered trials

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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.