Evidence map›Paper›PMID 39070454›Full record

ArticleCureus2024

Sacubitril/Valsartan Improves Cardiac Function in Dialysis Patients.

Zaher Armaly, Amer Saffouri, Habib Kordahji, Munir Hamzeh, Elias Bishouty, Narmin Matar, Maha Zaher, Adel Jabbour, Dahud Qarawani

Abstract read
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

  1. Pooled it
  2. Article
  3. 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

9 authors.

Zaher ArmalyNephrology, Edinburgh Medical Missionary Society (EMMS) Nazareth Hospital, Nazareth, ISR.
Amer SaffouriInternal Medicine, Edinburgh Medical Missionary Society (EMMS) Nazareth Hospital, Nazareth, ISR.
Habib KordahjiCardiology, Clalit Health Services, Nazareth, ISR.
Munir HamzehNephrology, Edinburgh Medical Missionary Society (EMMS) Nazareth Hospital, Nazareth, ISR.
Elias BishoutySurgery, Carmel Medical Center, Haifa, ISR.
Narmin MatarNephrology, Edinburgh Medical Missionary Society (EMMS) Nazareth Hospital, Nazareth, ISR.
Maha ZaherNephrology, Edinburgh Medical Missionary Society (EMMS) Nazareth Hospital, Nazareth, ISR.
Adel JabbourBiomedical Laboratory, Edinburgh Medical Missionary Society (EMMS) Nazareth Hospital, Nazareth, ISR.
Dahud QarawaniCardiology, Edinburgh Medical Missionary Society (EMMS) Nazareth Hospital, Nazareth, ISR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heart failure (HF) is characterized by the activation of adverse neurohormonal systems and a high mortality rate. Noteworthy, HF is a well-known complication of chronic kidney disease (CKD), especially in end-stage kidney disease (ESKD), where dialysis patients are seven to eight times more likely to encounter cardiac arrest than the general population. Therefore, it is important to develop efficient treatments to improve cardiac function in dialysis patients and eventually reduce the cardiovascular death toll. Sacubitril/valsartan (Sac/Val) is a dual inhibitor/blocker of the neprilysin and angiotensin II receptors, which exert cardioprotective effects among patients with heart failure with reduced ejection fraction (HFrEF) and heart failure with preserved EF (HFpEF). Unfortunately, the drug is not approved for subjects with advanced CKD or dialysis patients due to safety concerns. The current study examined the cardiac effects of Sac/Val in HD patients. Administration of Sac/Val (100-400 mg/day) to 12 hemodialysis (HD) patients with HFrEF for six months gradually improved ejection fraction (EF) independently of morphological changes in cardiac geometry, as assessed by echocardiography (ECHO), and hemodynamic alterations. Interestingly, the Cardiomyopathy Questionnaire (Kansas City KCCQ-12) revealed that quality of life significantly improved after Sac/Val treatment. No major adverse effects were reported in the present study, supporting the safety of Sac/Val at least in these patients and for the applied follow-up period. Collectively, these findings support the use of Sac/Val as a cardioprotective agent in both HD and peritoneal dialysis (PD) patients. Yet, a more comprehensive study is required to establish these findings and to extend the follow-up period for 12 months in order to solidify these encouraging results.

Indexed as

dialysisend-stage renal disease (esrd)heart failure with reduced ejection fractionheath-related quality of lifesacubitril/valsartan

Identifiers

PMID39070454
PMCPMC11283675

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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.