Evidence map›Paper›PMID 32151119›Full record

Trial reportTurkish journal of medical sciences2020

Effects of oral/enteral nutrition alone versus plus pantoprazole on gastrointestinal bleeding in critically ill patients with low risk factor: a multicenter, randomized controlled trial

Kürşat Gündoğan, Emre Karakoc, Turgut Teke, Avşar Zerman, Aliye Esmaoglu, Şahin Temel, Muhammet Güven, Murat Sungur

Abstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Turkish journal of medical sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Guideline
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. 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.

Kürşat GündoğanDivision of Intensive Care, Department of Internal Medicine, Faculty of Medicine, Erciyes University, Kayseri, TurkeyORCID 0000-0002-8433-3480
Emre KarakocDivision of Intensive Care, Department of Internal Medicine, Faculty of Medicine, Çukurova University, Adana, TurkeyORCID 0000-0002-4307-4603
Turgut TekeDivision of Intensive Care, Department of Pulmonary Disease, Faculty of Medicine, Necmettin Erbakan University, Konya, TurkeyORCID 0000-0001-5955-6255
Avşar ZermanIntensive Care Unit, Department of Internal Medicine, Ministry of Health Adana Numune Training and Educational Hospital, Adana, TurkeyORCID 0000-0003-0957-0766
Aliye EsmaogluDivision of Intensive Care, Department of Anesthesiology and Reanimation, Faculty of Medicine, Erciyes University, Kayseri, TurkeyORCID 0000-0002-8267-138X
Şahin TemelDivision of Intensive Care, Department of Internal Medicine, Faculty of Medicine, Erciyes University, Kayseri, TurkeyORCID 0000-0002-2766-4312
Muhammet GüvenDivision of Intensive Care, Department of Internal Medicine, Faculty of Medicine, Erciyes University, Kayseri, TurkeyORCID 0000-0001-9874-7185
Murat SungurDivision of Intensive Care, Department of Internal Medicine, Faculty of Medicine, Erciyes University, Kayseri, TurkeyORCID 0000-0002-0011-3166

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: Critically ill patients are at risk of developing gastrointestinal (GI) bleeding due to stress causing mucosal damage. Aim of the study was to determine the effect of oral/enteral nutrition with or without concomitant pantoprazole on upper GI bleeding in low risk critically ill patients. Materials and methods: This was a prospective, randomized, open-label, multicenter study conducted with intensive care unit (ICU) patients receiving oral/enteral nutritional support. Patients were randomly assigned into two groups including intervention group (received oral/EN plus pantoprazole) and control group (received only oral/EN). Results: A total of 300 patients (intervention group: 152, control group: 148) participated in the study. Overall, 226 (75%) patients were fed by orally and 74 (25%) patients fed by enteral tube feeding. Median duration of nutritional support 4 (range: 2–33) days. Overt upper GI bleeding was noted only in one patient (0.65%) who was in the intervention group. The overall length of ICU stay of 4 (2–105) days, while ICU stay was significantly longer in the intervention group than in the control group (P = 0.006). Conclusions: Our findings seems to indicate that in patients who are at low risk for GI bleeding and under oral/enteral nutritional support, the use of PPIs may not reduce the risk of bleeding, however these results are imprecise because of low event (GI bleeding) rate and limited power.

Indexed as

AgedAnti-Ulcer AgentsCritical CareCritical IllnessEnteral NutritionFemaleGastrointestinal HemorrhageHumansMaleMiddle AgedPantoprazoleProspective StudiesRiskTreatment OutcomeAnti-Ulcer AgentsPantoprazoleCritical illnessenteral nutritiongastrointestinal bleedingpantoprazolestress ulcer

Identifiers

PMID32151119
PMCPMC7379460

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.