Evidence map›Paper›PMID 38550516›Full record

ArticleFrontiers in cardiovascular medicine2024

The "arrhythmic" presentation of peripartum cardiomyopathy: case series and critical review of the literature.

Giovanni Peretto, Emanuele Micaglio, Giuseppe Ciconte, Marianna Maia, Martina Luzzi, Marianna Cariello, Adele Gabriella Rosa Bonfanti, Davide Lazzeroni, Luigi Anastasia, Paolo Cavoretto and 3 more

Abstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2024. 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
–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

4 citing papers in PubMed.

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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

13 authors.

Giovanni Peretto *Cardiac Electrophysiology and Clinical Arrhythmology Department, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Emanuele Micaglio *Department of Cardiac Electrophysiology and Clinical Arrhythmology, IRCCS Policlinico San Donato, Milan, Italy.
Giuseppe CiconteSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Marianna MaiaSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Martina LuzziSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Marianna CarielloSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Adele Gabriella Rosa BonfantiSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Davide LazzeroniDepartment of Cardiology, IRCCS Fondazione Don Carlo Gnocchi, Parma, Italy.
Luigi AnastasiaSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Paolo CavorettoSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Alaide ChieffoSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Paolo Della BellaCardiac Electrophysiology and Clinical Arrhythmology Department, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Carlo PapponeSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripartum Cardiomyopathy (PPCM) is a polymorphic myocardial disease occurring late during pregnancy or early after delivery. While reduced systolic function and heart failure (HF) symptoms have been widely described, there is still a lack of reports about the arrhythmic manifestations of the disease. Most importantly, a broad range of unidentified pre-existing conditions, which may be missed by general practitioners and gynecologists, must be considered in differential diagnosis. The issue is relevant since some arrhythmias are associated to sudden cardiac death occurring in young patients, and the overall risk does not cease during the early postpartum period. This is why multimodality diagnostic workup and multidisciplinary management are highly suggested for these patients. We reported a series of 16 patients diagnosed with PPCM following arrhythmic clinical presentation. Both inpatients and outpatients were identified retrospectively. We performed several tests to identify the arrhythmic phenomena, inflammation and fibrosis presence. Cardiomyopathies phenotypes were reclassified in compliance with the updated ESC guidelines recommendations. Arrhythmias were documented in all the patients during the first cardiological assessment. PVC were the most common recorder arrhythmias, followed by VF, NSVT, AF, CSD.

Indexed as

genetic predisposition to adverse cardiac outcomesmultidisciplinary managementmultimodal diagnostic approachPPCMpregnancyventricular arrhythmias

Identifiers

PMID38550516
PMCPMC10972901

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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.