Evidence map›Paper›PMID 30403664›Full record

ArticlePloS one2018

Comparison of clinical symptoms, gastric motility and fat intake in the early chronic pancreatitis patients with anti-acid therapy-resistant functional dyspepsia patients.

Mako Wakabayashi, Seiji Futagami, Hiroshi Yamawaki, Atsushi Tatsuguchi, Keiko Kaneko, Shuhei Agawa, Kazutoshi Higuchi, Noriko Sakasegawa, Makoto Murakami, Teppei Akimoto and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 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

17 authors at 2 institutions in 1 country.

Mako WakabayashiDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Seiji FutagamiDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.ORCID 0000-0003-0502-8646
Hiroshi YamawakiDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Atsushi TatsuguchiDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Keiko KanekoDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Shuhei AgawaDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Kazutoshi HiguchiDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Noriko SakasegawaDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Makoto MurakamiDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Teppei AkimotoDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Yasuhiro KodakaDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Nobue UekiDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Kaya GudisDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Chiaki KawamotoDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Takashi AkamizuThe First Department of Medicine, Wakayama Medical Unversity, Wakayama, Japan.
Choitsu SakamotoDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Katsuhiko IwakiriDepartment of Internal Medicine, Division of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Nippon Medical School · JPWakayama Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere was no available data concerning the clinical differentiation between the updated definition of early chronic pancreatitis (ECP) and anti-acid therapy-resistant functional dyspepsia (RFD).

aimsWe aimed to determine whether clinical symptoms, gastric motility, psychogenic factors and fat intake can help distinguish early chronic pancreatitis (ECP) from anti-acid therapy-resistant functional dyspepsia patients with pancreatic enzyme abnormalities (RFD-P) and anti-acid therapy-resistant functional dyspepsia (RFD) patients using endosonography.

methodsWe enrolled 102 consecutive patients presenting with typical symptoms of RFD patients (n = 52), ECP patients (n = 25) and RFD-P patients (n = 25). ECP patients were diagnosed based on the criteria recommended by the Japan Pancreatic Association. Gastric motility was evaluated by 13C-acetate breath tests. Severity of duodenal inflammation was examined.

results24.5% of RFD patients were determined as ECP using endosonography. Abdominal pain score in Gastrointestinal Symptom Rating Scale (GSRS) in the patients with ECP was significantly lower compared to that in the patients with RFD-P. There were no significant differences in State-Trait Inventory (STAI)-state/-trait scores, Self-Rating Questionnaire for Depression (SRQ-D) scores and clinical symptoms for fat intake among three groups. The early phase of gastric emptying (AUC5; AUC15) in ECP and RFD-P patients were significantly disturbed compared to those in RFD patients.

conclusionsEvaluation of severity of abdominal pain and measurement of the early phase of gastric emptying will be useful tools to distinguish ECP patients from RFD patients. Accurate diagnosis of ECP patients may contribute to the prevention from advancing of chronic pancreatitis.

Indexed as

Dietary FatsGastrointestinal MotilityAdultAnti-Ulcer AgentsDisease ManagementDrug ResistanceDyspepsiaEndosonographyFemaleGastric EmptyingHumansMaleMiddle AgedPancreatic Function TestsPancreatitis, ChronicRisk FactorsAnti-Ulcer AgentsDietary Fats

Identifiers

PMID30403664
PMCPMC6221270
OpenAlexW2899816729

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.