Evidence map›Paper›PMID 38826939›Full record

ArticleCureus2024

Cardiovascular Autonomic Deficits in Different Types of Achalasia.

Abhijith Anil, Ritesh K Netam, Atanu Roy, Dinu S Chandran, Ashok Kumar Jaryal, Govind K Makharia, Rajinder Parshad, Kishore K Deepak

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 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

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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. Article
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

8 authors.

Abhijith AnilDepartment of Physiology, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.
Ritesh K NetamDepartment of Physiology, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.
Atanu RoyDepartment of Physiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, IND.
Dinu S ChandranDepartment of Physiology, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.
Ashok Kumar JaryalDepartment of Physiology, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.
Govind K MakhariaDepartment of Gastroenterology and Human Nutrition, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.
Rajinder ParshadDepartment of Surgical Disciplines, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.
Kishore K DeepakDepartment of Physiology, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and objective Achalasia cardia is a primary esophageal motility disorder, and the etiopathology of this disease's progression is not known. Moreover, autonomic dysfunction has not been studied in different types of achalasia. In light of this, we aimed to address this lack of data in this study. Methods The diagnosis of achalasia was done using high-resolution esophageal manometry (HRM)-based Chicago classification v4.0. Autonomic function tests (AFT) such as the head-up tilt test, deep breathing test (DBT), Valsalva maneuver (VM), handgrip test (HGT), and cold pressor test (CPT), as well as the heart rate variability (HRV) test, were performed among the cohort and the results were compared with those of 39 age- and sex-matched healthy controls. Results AFT and HRV tests were done on 62 patients (30 achalasia type I, 28 type II, and 4 type III) and compared with 39 age- and sex-matched healthy controls. The mean duration of symptoms, high Eckardt score, and dysphagia were most common in type I achalasia, followed by type II and III. The results of AFT showed a generalized loss of parasympathetic and baroreflex-independent sympathetic reactivity in all types of achalasia. However, baroreflex-dependent cardiovascular adrenergic reactivity was normal. Regarding cardiac autonomic tone, there was a loss of parasympathetic and sympathetic influence, but sympathovagal balance was maintained. The severity of the loss of autonomic functions was higher in type I, followed by type II. Conclusions In all types of achalasia, parasympathetic reactivity, baroreflex-independent sympathetic reactivity, and cardiac autonomic tone were lower compared to healthy controls, and the severity of dysfunction increased during the progression of the disease from type II to type I.

Indexed as

achalasia cardiacardiac autonomic functionheart rate variability (hrv)high resolution esophageal manometrylower esophageal sphincter (les)

Identifiers

PMID38826939
PMCPMC11140828

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