Evidence map›Paper›PMID 38569478›Full record

ArticleDigestive diseases (Basel, Switzerland)2024

Improved Nutritional Outcomes and Gastrointestinal Symptoms in Adult Cystic Fibrosis Patients Treated with Elexacaftor/Tezacaftor/Ivacaftor.

Nela Stastna, Lumir Kunovsky, Michal Svoboda, Eva Pokojova, Lukas Homola, Miriam Mala, Zaneta Gracova, Barbora Jerabkova, Jana Skrickova, Jan Trna

Open access · hybridAbstract read
In one paragraph

Article in Digestive diseases (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
10.1field-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

11 citing papers in PubMed, 24 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Nela StastnaDepartment of Pneumology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czechia.
Lumir KunovskyFaculty of Medicine, Masaryk University, Brno, Czechia.
Michal SvobodaFaculty of Medicine, Masaryk University, Brno, Czechia.
Eva PokojovaFaculty of Medicine, Masaryk University, Brno, Czechia.
Lukas HomolaFaculty of Medicine, Masaryk University, Brno, Czechia.
Miriam MalaFaculty of Medicine, Masaryk University, Brno, Czechia.
Zaneta GracovaDepartment of Children's Infectious Diseases, University Hospital Brno, Brno, Czechia.
Barbora JerabkovaDepartment of Children's Infectious Diseases, University Hospital Brno, Brno, Czechia.
Jana SkrickovaFaculty of Medicine, Masaryk University, Brno, Czechia.
Jan TrnaFaculty of Medicine, Masaryk University, Brno, Czechia.
Masaryk University · CZUniversity Hospital Brno · CZCharles University · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCystic fibrosis transmembrane conductance regulator modulator therapy improves nutritional status and quality of life. Clinical trials have shown pancreatic insufficiency conversion, mostly in pediatric patients treated with ivacaftor. Studies with elexacaftor/tezacaftor/ivacaftor (ETI) in older patients have not suggested restoration of exocrine pancreas function, but quality data in adults are lacking. Our aim was to show the effect of ETI in adults with cystic fibrosis (CF) on nutritional status and digestive function. We hypothesized improvement of nutritional parameters and gastrointestinal symptoms, reduction of pancreatic enzyme replacement therapy, but uncertain improvement in exocrine pancreatic function.

methodsWe prospectively enrolled adults with CF treated with ETI from August 2021 to June 2022. We measured anthropometric parameters, laboratory nutritional markers, change of fecal elastase, pancreatic enzymes replacement therapy needs, and gastrointestinal symptoms.

resultsIn the cohort of 29 patients (mean age 29.1 years), 82.8% suffered exocrine pancreatic insufficiency. After ETI, mean BMI increased by 1.20 kg/m2 (p < 0.001), mean body weight by 3.51 kg (p < 0.001), albumin by 2.81 g/L, and prealbumin by 0.06 (both p < 0.001). Only 1 patient, initially pancreatic insufficient (4.5%, p < 0.001), developed pancreatic sufficiency, indicated by increased fecal elastase from 45 μg/g to 442.1 μg/g. Mean change in lipase substitution decreased by 1,969 units/kg/day (p < 0.001) and stools frequency by 1.18 per day (p < 0.001).

conclusionOur data suggest increased nutritional parameters, lower pancreatic substitution requirements, and improved defecation in adult CF patients on ETI. Improvement in exocrine pancreatic function might be mutation-specific and needs further study.

Indexed as

Cystic FibrosisDrug CombinationsExocrine Pancreatic InsufficiencyIndolesNutritional StatusAdultAminophenolsBenzodioxolesFemaleGastrointestinal DiseasesHumansMalePancreatic ElastaseProspective StudiesPyrazolesPyridinesAminophenolsBenzodioxolesDrug Combinationselexacaftorelexacaftor, ivacaftor, tezacaftor drug combinationIndolesPancreatic ElastasePyrazolesPyridinesPyrrolidinesQuinolinesQuinolonesCystic fibrosisElexacaftor/tezacaftor/ivacaftorExocrine pancreas functionNutritionPancreatic enzyme replacement therapy

Identifiers

PMID38569478
PMCPMC11250406
OpenAlexW4394766685

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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.