Evidence map›Paper›PMID 31007939›Full record

ArticleBMC nutrition2019

A Survey Identifying Nutritional Needs in a Contemporary Adult Cystic Fibrosis Cohort.

Siddhartha G Kapnadak, Kathleen J Ramos, Andrea M Lopriore, Christopher H Goss, Moira L Aitken

Abstract read
In one paragraph

Article in BMC nutrition, 2019. 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
–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

1 citing paper in PubMed.

  1. 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

5 authors.

Siddhartha G KapnadakDepartment of Medicine; Division of Pulmonary, Critical Care, and Sleep Medicine, University of Washington School of Medicine, 1959 NE Pacific, Campus Box 356522, Seattle, WA, USA 98195-6522.
Kathleen J RamosDepartment of Medicine; Division of Pulmonary, Critical Care, and Sleep Medicine, University of Washington School of Medicine, 1959 NE Pacific, Campus Box 356522, Seattle, WA, USA 98195-6522.
Andrea M LoprioreDepartment of Nutrition, Division of Pulmonary and Sleep Medicine, University of Washington School of Medicine, 1959 NE Pacific, Campus Box 356522, Seattle, WA, USA 98195-6522.
Christopher H GossDepartment of Medicine; Division of Pulmonary, Critical Care, and Sleep Medicine, University of Washington School of Medicine, 1959 NE Pacific, Campus Box 356522, Seattle, WA, USA 98195-6522.
Moira L AitkenDepartment of Medicine; Division of Pulmonary, Critical Care, and Sleep Medicine, University of Washington School of Medicine, 1959 NE Pacific, Campus Box 356522, Seattle, WA, USA 98195-6522.

Funding

Translational Research Center to Expedite Novel Therapies in Cystic FibrosisP30DK089507 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Christopher Hooper Goss · 2010 to 2026
$21.4M
Predicting survival and planning for lung transplantation in severe cystic fibrosisK23HL138154 · NHLBI · UNIVERSITY OF WASHINGTON · PI RAMOS, KATHLEEN JESSICA · 2017 to 2021
$947k
NHLBI NIH HHS K23 HL138154NIDDK NIH HHS P30 DK089507
6 · The paper itself

Abstract

backgroundCystic fibrosis (CF) is a disease in which nutritional barriers are diverse and common, with malnutrition greatly influencing pulmonary trajectory and overall outcomes. Despite this, the most effective methods to optimize CF nutrition are unknown, and literature describing patients' perspectives on their specific nutritional needs is lacking, particularly in the modern era of CF care. This study aimed to identify the most important nutritional needs and desired health-improvement resources in a contemporary adult CF cohort.

methodsA 14-question investigator-designed survey addressing nutrition concerns, preferred health-improvement resources, and dietary/exercise routines was administered to CF adults. Clinical characteristics and survey responses are presented with descriptive statistics, and responses compared by body mass index (BMI) category (<18.5 kg/m

resultsOf 66 total patients, nine (13.6%) were underweight (BMI <18.5 kg/m

conclusionsWe identified a wide variety of nutritional needs in CF adults, including a high prevalence of overweight status, many patients desiring weight loss, and many seeking financial resources. Our findings support the individualization of modern-day CF nutrition programs and development of online resources, in an effort to address the heterogeneous barriers that exist in the contemporary CF population and improve outcomes in patients with the disease.

Indexed as

body compositionbody mass indexcomplicationsCystic fibrosismalnutritionnutrition assessmentnutrition therapyobesity

Identifiers

PMID31007939
PMCPMC6474380

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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.