Evidence map›Paper›PMID 38577740›Full record

GuidelinePediatrics2024

Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID.

Deanna M Green, Thomas Lahiri, Karen S Raraigh, Fadel Ruiz, Jacquelyn Spano, Nicholas Antos, Lynn Bonitz, Lillian Christon, Myrtha Gregoire-Bottex, Jaime E Hale and 20 more

Open access · greenAbstract readPractice GuidelineSystematic Review
In one paragraph

Guideline in Pediatrics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
10.9field-weighted citation impact, top 1% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Guideline
  2. Review
  3. Article
  4. Article
  5. Review
  6. Transforming Care Models in Cystic Fibrosis: A Review.Healthcare (Basel, Switzerland) · 2025
    Review
  7. Article
  8. Article
  9. Cystic Fibrosis Year in Review 2024.Pediatric pulmonology · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
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

30 authors at 20 institutions in 3 countries.

Deanna M Green *Johns Hopkins All Children's Hospital, St Petersburg, Florida.
Thomas LahiriUniversity of Vermont Children's Hospital, Burlington, Vermont.
Karen S RaraighJohns Hopkins University School of Medicine, Baltimore, Maryland.
Fadel RuizBaylor College of Medicine.
Jacquelyn SpanoStanford University School of Medicine, Stanford, California.
Nicholas AntosMedical College of Wisconsin, Children's Wisconsin, Milwaukee, Wisconsin.
Lynn BonitzCohen Children's Medical Center of NY/Northwell Health, New Hyde Park, New York.
Lillian ChristonMedical University of South Carolina, Charleston, South Carolina.
Myrtha Gregoire-BottexAdvanced Pediatric Pulmonology, Pllc, Miramar, Florida.
Jaime E HaleUniversity of Massachusetts Chan Medical School, Worcester, Massachusetts.
Elinor Langfelder-SchwindLenox Hill Hospital/Northwell Health, New York, New York.
Álvaro La Parra PerezJohn B. Goddard School of Business and Economics, Weber State University, Ogden, Utah.
Karen MaguinessRiley Hospital for Children at IU Health, Indianapolis, Indiana.
John MassieUniversity of Melbourne Murdoch Childrens Research Institute, Melbourne, Australia.
Erin McElroy-BarkerRutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey.
Meghan E McGarryUniversity of California San Francisco, San Francisco, California.
Angelique MercierRobert H. Lurie Children's Hospital of Chicago, Northwestern University, Feinberg School of Medicine, Chicago, Illinois.
Anne MunckHospital Necker Enfants malades, AP-HP, Paris, France.
Kathryn E OliverEmory University School of Medicine, Atlanta, Georgia.
Staci SelfUniversity of Alabama at Birmingham, Birmingham, Alabama.
Kathryn SinghUniversity of California, Irvine, Orange, California Miller Children's and Women's Hospital, Long Beach, California.
Michael SmileySaint Louis University, St Louis, Missouri.
Steven SnodgrassPrisma Health Children's Hospital, Greenville, South Carolina.
Audrey TluczekUniversity of Wisconsin-Madison, Madison, Wisconsin.
Pamela TuleyTexas Children's Hospital, Houston, Texas.
Paula LomasThe Cystic Fibrosis Foundation, Bethesda, Maryland.
Elise WongThe Cystic Fibrosis Foundation, Bethesda, Maryland.
Sarah E HempsteadThe Cystic Fibrosis Foundation, Bethesda, Maryland.
Albert FaroThe Cystic Fibrosis Foundation, Bethesda, Maryland.
Clement L Ren *The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Cystic Fibrosis Foundation · USJohns Hopkins University · USNorthwell Health · USBaylor College of Medicine · USChildren's Hospital of Philadelphia · USChildren's Hospital of Wisconsin · USEmory University · USHealth Net · USHôpital Necker-Enfants Malades · FRJohnson University · USMedical University of South Carolina · USMiller Children's & Women's Hospital · USNorthwestern University · USPrisma Health · USRiley Hospital for Children · USSaint Louis University · USStanford University · USTexas Children's Hospital · USUniversity of Alabama at Birmingham · USUniversity of California, San Francisco · US

Funding

Risk Factors For Worse Lung Function In Latinos With Cystic FibrosisK23HL133437 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCGARRY, MEGHAN ELIZABETH · 2018 to 2023
$1.0M
NHLBI NIH HHS K23 HL133437NIMHD NIH HHS L60 MD010865
6 · The paper itself

Abstract

A multidisciplinary committee developed evidence-based guidelines for the management of cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen-positive, inconclusive diagnosis (CRMS/CFSPID). A total of 24 patient, intervention, comparison, and outcome questions were generated based on surveys sent to people with CRMS/CFSPID and clinicians caring for these individuals, previous recommendations, and expert committee input. Four a priori working groups (genetic testing, monitoring, treatment, and psychosocial/communication issues) were used to provide structure to the committee. A systematic review of the evidence was conducted, and found numerous case series and cohort studies, but no randomized clinical trials. A total of 30 recommendations were graded using the US Preventive Services Task Force methodology. Recommendations that received ≥80% consensus among the entire committee were approved. The resulting recommendations were of moderate to low certainty for the majority of the statements because of the low quality of the evidence. Highlights of the recommendations include thorough evaluation with genetic sequencing, deletion/duplication analysis if <2 disease-causing variants were noted in newborn screening; repeat sweat testing until at least age 8 but limiting further laboratory testing, including microbiology, radiology, and pulmonary function testing; minimal use of medications, which when suggested, should lead to shared decision-making with families; and providing communication with emphasis on social determinants of health and shared decision-making to minimize barriers which may affect processing and understanding of this complex designation. Future research will be needed regarding medication use, antibiotic therapy, and the use of chest imaging for monitoring the development of lung disease.

Indexed as

Cystic FibrosisEvidence-Based MedicineCystic Fibrosis Transmembrane Conductance RegulatorGenetic TestingHumansNeonatal ScreeningCystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID38577740
PMCPMC11781860
OpenAlexW4393982752

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.