Evidence map›Paper›PMID 29717405›Full record

ArticleObesity surgery2018

Risk of GERD-Related Disorders in Obese Patients on PPI Therapy: a Population Analysis.

Simon Erridge, Osama M Moussa, Paul Ziprin, Ara Darzi, Sanjay Purkayastha

Open access · hybridAbstract read
In one paragraph

Article in Obesity surgery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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

5 authors at 1 institution in 1 country.

Simon ErridgeDepartment of Surgery and Cancer, Division of Surgery, Academic Surgical Unit, St. Mary's Hospital, Imperial College London, 10th Floor QEQM, South Wharf Road, London, W2 1NY, UK.ORCID 0000-0001-5871-6501
Osama M MoussaDepartment of Surgery and Cancer, Division of Surgery, Academic Surgical Unit, St. Mary's Hospital, Imperial College London, 10th Floor QEQM, South Wharf Road, London, W2 1NY, UK. o.moussa@imperial.ac.uk.
Paul ZiprinDepartment of Surgery and Cancer, Division of Surgery, Academic Surgical Unit, St. Mary's Hospital, Imperial College London, 10th Floor QEQM, South Wharf Road, London, W2 1NY, UK.
Ara DarziDepartment of Surgery and Cancer, Division of Surgery, Academic Surgical Unit, St. Mary's Hospital, Imperial College London, 10th Floor QEQM, South Wharf Road, London, W2 1NY, UK.
Sanjay PurkayasthaDepartment of Surgery and Cancer, Division of Surgery, Academic Surgical Unit, St. Mary's Hospital, Imperial College London, 10th Floor QEQM, South Wharf Road, London, W2 1NY, UK.
St Mary's Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIncreasing prevalence of obesity has shown an associated increase in gastroesophageal reflux disease (GERD)-related diseases. Proton pump inhibitor (PPI) therapy has been demonstrated to reduce the incidence of such diseases. The study's aim was to analyze the Clinical Practice Research Datalink (CPRD) to determine factors that increase the propensity of obese patients on PPIs to develop Barrett's esophagus (BE) and esophageal carcinoma.

methodA case-control population study was carried out, including patients from the CPRD. Clinicopathological factors were extracted for each patient alongside clinical endpoints of GERD, BE, and esophageal carcinoma. Multivariate analysis was utilized to identify factors that increase the propensity to develop BE and esophageal carcinoma. Statistical significance was p < 0.050.

resultsOne hundred sixty five thousand nine hundred twenty nine obese patients on PPI treatment were identified up until July 2017. Median follow-up time was 119.0 months (range 11.3-1397.9 months). In patients with GERD, the following were associated with increased BE risk: age ≥ 60 years (OR = 1.197; p = 0.039), male (OR = 2.209; p < 0.001), H2 antagonists (OR = 1.377; p < 0.001), D2 antagonists (OR = 1.241; p = 0.008), and hiatus hernias (OR = 6.772; p = 0.017). The following were associated with increased risk of esophageal carcinoma: age (OR = 2.831; p = 0.031), male sex (OR = 3.954; p = 0.003), and hiatus hernias (OR = 12.170; p < 0.001). Only D2 antagonists (OR = 2.588; p = 0.002) were associated with increased risk of developing esophageal carcinoma in BE patients.

conclusionsIn obese patients on PPI therapy for reflux, higher BMIs were not associated with increased risk of BE or esophageal carcinoma. Males, older patients, and those with hiatus hernias are at increased risk of developing BE and carcinoma. Failure of PPI monotherapy is predictive of future metaplasia and dysplasia.

Indexed as

Gastroesophageal RefluxObesityBarrett EsophagusCase-Control StudiesEsophageal NeoplasmsFemaleHumansMaleMiddle AgedProton Pump InhibitorsRisk FactorsProton Pump InhibitorsBarrett’s esophagusEsophageal carcinomaGERDObesity

Identifiers

PMID29717405
PMCPMC6132732
OpenAlexW2801157127

What OpenQuestion holds

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LicenceCC BY
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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.