Evidence map›Paper›PMID 35070791›Full record

ArticleCardiovascular diagnosis and therapy2021

Sacubitril/valsartan in everyday clinical practice: an observational study based on the experience of a heart failure clinic.

Joana Cabral, Henrique Vasconcelos, Paulo Maia-Araújo, Emília Moreira, Manuel Campelo, Sandra Amorim, Alexandra Sousa, Brenda Moura, Roberto Pinto, Camila Dias and 1 more

Open access · diamondAbstract read
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Article in Cardiovascular diagnosis and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 11 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

11 authors at 4 institutions in 1 country.

Joana CabralFaculty of Medicine, University of Porto, Porto, Portugal.
Henrique VasconcelosFaculty of Medicine, University of Porto, Porto, Portugal.
Paulo Maia-AraújoCINTESIS-Center for Health Technology and Services Research, Porto, Portugal.
Emília MoreiraCINTESIS-Center for Health Technology and Services Research, Porto, Portugal.
Manuel CampeloCINTESIS-Center for Health Technology and Services Research, Porto, Portugal.
Sandra AmorimCINTESIS-Center for Health Technology and Services Research, Porto, Portugal.
Alexandra SousaCINTESIS-Center for Health Technology and Services Research, Porto, Portugal.
Brenda MouraCINTESIS-Center for Health Technology and Services Research, Porto, Portugal.
Roberto PintoDepartment of Cardiology, Centro Hospitalar Universitário de São João, Porto, Portugal.
Camila DiasDepartment of Medicine, Faculty of Medicine, University of Porto, Porto, Portugal.
José Silva-CardosoCINTESIS-Center for Health Technology and Services Research, Porto, Portugal.
Universidade do Porto · PTCentre for Health Technology and Services Research · PTHospital das Forças ArmadasHospital de São João · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeart failure (HF) is a growing public health problem. Sacubitril/valsartan is now recommended to be used in persistently symptomatic patients with left ventricular ejection fraction (LVEF) <40%, replacing angiotensin-converting enzyme inhibitors (ACEis)/angiotensin receptor blockers (ARBs). In the present study, we aimed to characterise the challenges of sacubitril/valsartan use in everyday clinical practice.

methodsWe assessed the medical records of patients with HF and reduced ejection fraction eligible for sacubitril/valsartan attending a HF clinic at a Portuguese University Hospital during 2018 (n=152). The number of eligible patients receiving the drug and the reasons for not prescribing sacubitril/valsartan were evaluated. Additionally, we assessed the tolerability of maximal doses of sacubitril/valsartan. New York Heart Association functional class (NYHA class) and LVEF before and after up-titration to maximal tolerated sacubitril/valsartan dose were compared. Median follow-up was 41 months.

resultsOf the 152 included patients, 75 (49%) were prescribed the drug. The two main reasons for non-prescription were patient financial barriers (31%) and hypotension (27%). Only 33% of patients on sacubitril/valsartan did reach maximal dose. Hypotension was the main limiting factor for dose optimisation. Duration of sacubitril/valsartan treatment showed a positive association with LVEF improvement during follow-up (6.6% absolute LVEF increase/year). NYHA functional class improved significantly from baseline through the end of follow-up.

conclusionsIn every-day clinical practice, although sacubitril/valsartan was associated with a marked improvement in NYHA class and in LVEF, important financial and clinical barriers to the implementation of this therapy were identified.

Indexed as

financial barriersheart failure (HF)neurohormonal modulationreal-life practiceSacubitril/valsartan

Identifiers

PMID35070791
PMCPMC8748480
OpenAlexW3213620301

What OpenQuestion holds

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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.