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Efficacy and safety of proton pump inhibitors for stress ulcer prophylaxis in critically ill patients: a systematic review and meta-analysis of randomized trials

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  • 3, 4,
  • 3,
  • 1,
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  • 1, 3, 7Email author
Critical Care201620:120

https://doi.org/10.1186/s13054-016-1305-6

©  Alshamsi et al. 2016

  • Received: 20 March 2016
  • Accepted: 19 April 2016
  • Published:

Abstract

Background

The relative efficacy and safety of proton pump inhibitors (PPIs) compared to histamine-2-receptor antagonists (H2RAs) should guide their use in reducing bleeding risk in the critically ill.

Methods

We searched the Cochrane library, MEDLINE, EMBASE, ACPJC, clinical trials registries, and conference proceedings through November 2015 without language or publication date restrictions. Only randomized controlled trials (RCTs) of PPIs vs H2RAs for stress ulcer prophylaxis in critically ill adults for clinically important bleeding, overt gastrointestinal (GI) bleeding, nosocomial pneumonia, mortality, ICU length of stay and Clostridium difficile infection were included. We used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach to assess our confidence in the evidence for each outcome.

Results

In 19 trials enrolling 2117 patients, PPIs were more effective than H2RAs in reducing the risk of clinically important GI bleeding (RR 0.39; 95 % CI 0.21, 0.71; P = 0.002; I 2  = 0 %, moderate confidence) and overt GI bleeding (RR 0.48; 95 % CI 0.34, 0.66; P < 0.0001; I 2  = 3 %, moderate confidence). PPI use did not significantly affect risk of pneumonia (RR 1.12; 95 % CI 0.86, 1.46; P = 0.39; I 2  = 2 %, low confidence), mortality (RR 1.05; 95 % CI 0.87, 1.27; P = 0.61; I 2  = 0 %, moderate confidence), or ICU length of stay (mean difference (MD), –0.38 days; 95 % CI –1.49, 0.74; P = 0.51; I 2  = 30 %, low confidence). No RCT reported Clostridium difficile infection.

Conclusions

PPIs were superior to H2RAs in preventing clinically important and overt GI bleeding, without significantly increasing the risk of pneumonia or mortality. Their impact on Clostridium difficile infection is yet to be determined.

Keywords

  • Clostridium Difficile Infection
  • Clostridium Difficile
  • Moderate Confidence
  • Stress Ulcer
  • Intensive Care Unit Length

Background

Over four decades ago, investigators first described stress ulcer bleeding in critically ill patients [1]. Since then, multiple studies have described this condition and its impact on the prognosis of critically ill patients. Stress ulcers typically occur in the gastric body, esophagus, or duodenum, sometimes resulting in gastrointestinal (GI) bleeding. Earlier studies reported overt GI bleeding in 5 to 25 % of critically ill patients [2, 3]. In contrast, the incidence of clinically important GI bleeding is much lower, estimated between 1 and 4 % [2, 4–7]. A recent large observational study (1034 patients, 97 sites), reported a 2.6 % incidence of clinically important GI bleeding [7], which was previously found to be associated with increased intensive care unit (ICU) mortality and length of stay [8]. Despite reduction in clinically important GI bleeding, pharmacologic stress ulcer prophylaxis does not seem to affect mortality in randomized controlled trials (RCTs) [8].

RCTs have investigated different classes of medication for stress ulcer prophylaxis. Recently, a meta-analysis of 29 RCTs showed that prophylaxis with either proton pump inhibitors (PPIs) or histamine-2-receptor antagonists (H2RAs) was associated with lower risk of overt GI bleeding compared to placebo or no prophylaxis [9]. However, the relative effectiveness of the two classes of agent remains uncertain.

PPIs, more potent at increasing gastric pH than H2RAs and maintaining gastric pH between 3.5 and 5.0, may minimize the risk of gastric mucosal injury [10]. Of four meta-analyses comparing PPIs to H2RAs, three suggested that PPIs are superior to H2RAs [11–13] and one did not [14].

The Surviving Sepsis Campaign (SSC) guidelines recommend using stress ulcer prophylaxis among critically ill patients with risk factors (e.g., mechanically ventilated patients, and patients with coagulopathy), including a weak recommendation for using PPIs over H2RAs in this setting [15]. The advice is concordant with current practice: recent observational studies showed that PPIs are the most commonly used prophylactic agents in the ICU [16–18].

In terms of the relative impact of PPIs and H2RAs, adverse effects are also a concern. In particular, a recent large retrospective observational study suggested PPI versus H2RA use in critically ill patients was associated with higher risks of pneumonia and Clostridium difficile infection compared to H2RA [19]. These results are, however, limited by the observational study design.

Several RCTs have been published recently and may influence both risk of bias and precision [20–25]. Therefore, we conducted a systematic review and meta-analysis to evaluate the efficacy and safety of PPIs compared to H2RAs for stress ulcer prophylaxis in critically ill patients. We used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) methodology to assess the quality of evidence [26].

Methods

Study selection

Studies were eligible if: (1) the study design was an RCT; (2) the population involved adult critically ill patients in the ICU; (3) the intervention group received a PPI (either parenteral or enteral), regardless of the dose, frequency, or duration; (4) the control group received an H2RA, either parenteral or enteral, regardless of the dose, frequency, or duration; and (5) the outcomes included all or any of the following: clinically important GI bleeding; overt upper GI bleeding; pneumonia; mortality, ICU length of stay, and/or Clostridium difficile infection.

Search strategy

We updated our previous systematic review [12] and searched MEDLINE, EMBASE, Cochrane Library, ACPJC, and International Clinical Trial Registry Platform (ICTRP) from March 2012 through November 2015. Our search strategy is detailed in Additional file 1: Tables S3-S5. We screened citations of all new potentially eligible articles without language or publication date restrictions. We conducted an electronic search of conference proceedings via a website provided by McMaster University (http://library.mcmaster.ca/articles/proceedingsfirst). Two reviewers (FA and EB) screened titles and abstracts to identify articles for full review, and evaluated the full text of potentially eligible studies. Disagreements between reviewers were resolved by consensus, and if necessary, consultation with a third reviewer (WA).

Data extraction

Two reviewers (FA and EB) independently extracted pertinent data from all new studies utilizing a pre-designed data abstraction form. Disagreements were resolved by discussion and consensus. We contacted study authors for missing or unclear information.

Risk of bias assessment

Two reviewers (FA and EB) independently examined eligible trials for risk of bias using the Cochrane Collaboration tool [27]. For each included trial, we judged articles as having low, unclear, or high risk of bias for the domains of adequate sequence generation, allocation sequence concealment, blinding for objective outcomes, incomplete outcome data, selective outcome reporting, and for other bias. The overall risk of bias for each trial included was categorized as low if the risk of bias was low in all domains, unclear if the risk of bias was unclear in at least one domain and with no high risk of bias domain, or high if the risk of bias was high in at least one domain. We resolved disagreements by discussion and consensus.

Statistical analysis

We analyzed data using RevMan software (Review Manager, version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014). We used the DerSimonian and Laird [28] random-effects model to pool the weighted effect of estimates across all studies. We estimated study weights using the inverse variance method. We calculated pooled relative risks (RRs) for dichotomous outcomes and mean differences (MDs) for continuous outcomes, with corresponding 95 % confidence intervals (CIs). We assessed statistical heterogeneity using Chi2 and I 2 statistics [29]. We predefined substantial heterogeneity as P < 0.10 or I 2  > 50 %.

We calculated the number needed to treat (NNT) using the method proposed by the Cochrane Collaboration [30]. We used an assumed control group (ACR) event rate of 3 % for clinically important bleeding and 5 % for overt GI bleeding; these ACRs were based on the results of a recent observational study [7]. We inspected funnel plots and performed Egger’s test to assess publication bias [31]. We explored heterogeneity between studies by performing predetermined subgroup analyses to investigate whether certain factors influenced the treatment effect. These subgroups included high vs. low risk of bias (hypothesizing that studies with high risk of bias would have a larger treatment effect), PPI route of administration (hypothesizing that the treatment effect would be larger with parenteral administration), PPI dose (hypothesizing that treatment effect would be larger with higher dosing). In addition, we conducted a post hoc sensitivity analysis, excluding trials published in abstract form [20, 23, 32–35].

Results

Characteristics of studies included

Our new search identified a total of 255 citations. After removing duplicates, 214 articles remained. Following screening of titles and abstracts, 197 articles were excluded; 17 articles were retrieved for full text assessment and 11 were excluded for variable reasons (Fig. 1). After reviewing our previous results, we excluded an abstract [36] (n = 202) that was later published as a full article [35]. Another study was published as an abstract but was excluded from the analysis because the necessary data could not be obtained [37]. A total of six new trials (n = 600 patients) are included in the different analyses.
Fig. 1
Fig. 1

Process of identifying eligible studies: 18 trials (5 abstracts and 13 full published articles) were eligible and were included in the qualitative and quantitative analyses. RCT randomized controlled trial

Combining our previous and current results, 19 RCTs [20, 22–25, 32–35, 38–48] from 20 reports (one study published outcomes separately in two different reports) [47, 48] met eligibility criteria and were included. Two eligible trials were published in abstract form [32, 33]; further information was obtained after contacting the authors.

Of 19 eligible trials [20, 22–25, 32–35, 38–48], 6 were published as an abstract only [20, 23, 32–34, 38] (Table 1). Overall, the included RCTs enrolled 2117 critically ill patients with a wide spectrum of medical and surgical conditions. Ten trials used intravenous PPIs, and eight used enteral PPIs, and the route was not described in one trial, which was published in abstract form. [23] The definitions for bleeding and pneumonia varied across trials and are summarized in Table 1.
Table 1

Characteristics of trials included

Author

Population

Interventions

Definition of GI bleeding

Definition of pneumonia

Funding

Conrad [35]

USA

(n = 359)

MV patients with risk factors

Age (mean) 55.6 years

Male 59 %

APACHE II (mean) 23.7

Omeprazole 40 mg IV twice daily loading, then 40 mg daily (n = 178)

Cimetidine 300 mg IV bolus, then infusion at 50 mg/h (n = 181)

(1) Bright red blood not clearing after tube adjustment and lavage

(2) 8 h of persistent coffee grounds material with aspirates every 2 h not clearing with lavage or

(3) Persistent coffee grounds material over 2–4 h on day 3–14 in 3 consecutive aspirates not clearing with lavage

USFDA

Pharmaceutical

Azevedo [36]

Brazil

(n = 108)

Critically ill patients with risk factors

Age (mean) 56.7 years

Male 52 %

APAHE (mean) 55.3

Omeprazole 40 mg IV twice daily (n = 38)

Ranitidine 150 mg/day IV (n = 38)

Sucralfate 1 g PO four times daily (n = 32)

Overt bleeding

CDC criteria

NR

Hata [37]

Japan

(n = 210)

Cardiac surgery patients

Age (mean) 64.5 years

Male 73 %

APACHE II NR

Rabeprazole 10 mg PO daily (n = 70)

Ranitidine 300 mg PO daily (n = 70)

Teprenone 150 mg NG daily (n = 70)

Overt bleeding with endoscopic lesions

NA

NR

Kantorova [38]

Czech Republic

(n = 287)

Surgical ICU with risk factors

Age (mean) 47 years

Male 67 %

APACHE II (mean) 18.4

Omeprazole 40 mg IV daily (n = 72)

Famotidine 40 mg IV twice daily (n = 71)

Sucralfate 1 g PO four times daily (n = 69)

Placebo (n = 75)

Overt bleeding with one of the following:

(1) Drop in SBP >20 mmHg or rise in HR >20 beats/min within 24 h not explained by other causes or

(2) Drop in hemoglobin >2 g/dL not explained by other causes

New or progressive infiltrate and 3 of the following:

(1) Purulent ETT aspirate with >25 WBC/LPF

(2) Peripheral leukocytosis >11 × 109/or >10 % bands

(3) Temperature >38.5 °C

(4) Pathogen from aspirate, BAL (≥104 CFU/mL) or protected brush sampling (≥103 CFU/mL)

(5) Positive blood or pleural cultures

Pharmaceutical

Kotlyanskaya [31]

Abstract

USA (n = 66)

MV patients.

Age 71.2 years

Male NR

APACHE II 27.6

Lansoprazole (suspension) NG (n = 22)

Lansoprazole (tablet) NG (n = 23)

Ranitidine (n = 21) (dose and frequency not reported)

Overt bleeding associated with hemodynamic changes or Hb drop

NR

NR

Levy [39]

USA

(n = 67)

Medical and surgical ICU patients with risk factors.

Age 57.1 years

Male 55 %

APACHE II 18.9

Omeprazole 40 mg NG daily (n = 32)

Ranitidine 50 mg IV bolus, then 150 mg IV daily (n = 35)

Overt bleeding with hemodynamic instability, or a decrease Hb >2 g/dL requiring transfusion or associated with hemodynamic instability

NR

NR

Pan [40]

China

(n = 30)

Severe pancreatitis

Age 48 years

Male 45 %

APACHE II 12.2

Rabeprazole 20 mg PO daily (n = 20)

Famotidine 40 mg IV twice daily (n = 10)

Overt bleeding

NA

NR

Phillips [32]

Abstract

USA (n = 58)

MV patients with risk factors

Age NR

Male NR

APACHE II NR

Omeprazole 40 mg PO, then 20 mg PO daily (n = 33)

Ranitidine 50 mg IV loading, then 150–200 mg/day infusion (n = 25)

No clear definition

NR

NR

Powell [41]

UK

(n = 41)

Cardiac surgery

Age 56.5 years

Male 86 %

APACHE II NR

Omeprazole 80 mg IV bolus, then 40 mg IV bolus three times daily (n = 10)

Omeprazole 80 mg IV bolus then 40 mg IV infusion three times daily (n = 10)

Ranitidine 50 mg IV three times daily (n = 11) Placebo (n = 10)

Overt bleeding

NA

Academic

Risaliti [42]

Italy

(n = 28)

Surgical ICU

Age 61.5 years

Male 64 %

APACHE II NR

Omeprazole 40 mg IV daily, then 20 mg PO daily (n = 14)

Ranitidine 150 mg IV daily, then 300 mg PO daily (n = 14)

No clear definition

NA

NR

Solouki [43]

Iran

(n = 129)

MV patients with other risk factors.

Age 50.8 years

Male 52 %

APACHE II NR

Omeprazole 20 mg PO twice daily (n = 61)

Ranitidine 50 mg IV twice daily (n = 68)

Overt bleeding associated with one of the following:

(1) 20 mmHg decrease in SBP or DBP within 24 h or 20 beat/min increase in HR or postural drop by 10 mmHg in SBP

(2) 2 g/dL decrease in Hb or 6 % decrease in Hct within 24 h

(3) Lack of increase in Hb after two units of packed cells

New infiltrate and two of the following:

(1) Fever ≥38.3 °C

(2) WBC >10 × 109/L

(3) Pus in ETT aspirate

NR

Somberg [34]

USA

(n = 202)

Medical and surgical ICU patients with risk factors

Age 42 years

Male 74 %

APACHE II 15.2

Pantoprazole 40 mg IV daily (n = 32)

Pantoprazole 40 mg IV twice daily (n = 38)

Pantoprazole 80 mg IV daily (n = 23)

Pantoprazole 80 mg IV twice daily (n = 39)

Pantoprazole 80 mg IV three times daily (n = 35)

Cimetidine 300 mg IV bolus, then 50 mg/h infusion (n = 35)

(1) Hematemesis or bright red blood in gastric aspirate that did not clear after tube adjustment and 10-min lavage

(2) Persistent coffee ground material for 8 h that did not clear with lavage, or accompanied by 5 % decrease in Hct

(3) Decrease in Hct requiring ≥1 transfusions in the absence of obvious source or

(4) Melena or hematochizia

Radiological changes

Pharmaceutical

Fink [33]

Abstract

USA

(n = 189)

Adult critically ill patients

Age NR

Male NR

APACHE II 15

Pantoprazole 40 mg IV daily, 40 mg IV twice daily, 80 mg IV daily, or 80 mg IV twice daily (n = 158);

Cimetidine IV 300 mg bolus, then 50 mg/h infusion (n = 31)

No clear definition

NA

NR

Bashar [21]

Iran

(n = 120)

MV trauma patients, APACHE II < 25

Age 40.15

Male 7 %

APACHE II 15.2

Pantoprazole 40 mg IV daily then 40 mg PO daily when enteral feeds started (n = 60)

Ranitidine 50 mg IV three times daily while NPO then 150 mg PO daily when enteral feeds started (n = 60)

No clear definition

Clinical Pulmonary Infection Score (CPIS)

NR

Lee [23]

Taiwan

(n = 60)

Neurosurgical ICU

Age 57.7 years

Male 60 %

APACHE II 17.1

Esomeprazole 40 mg PO daily for 7 days (n = 30)

Famotidine 20 mg IV twice daily for 7 days (n = 30)

Overt bleeding, or decreased hemoglobin level >2 g/dL and lesions on endoscopy

>48 h of ventilation and 3 or more of:

(1) Persistent (>48 h) or new infiltrate

(2) Positive sputum smear

(3) Fever >38.3 °C

(4) WBC >12 × 109/L

Academic

Liu [24]

China

(n = 165)

Neurosurgical ICU with ICH

Age NA

Male 65 (58 %)

APACHE II NR

Omeprazole 40 mg IV twice daily (n = 58)

Cimetidine 300 mg IV four times daily (n = 54) Placebo (n = 53)

Overt bleeding that requires transfusion, with or without hemodynamic instability

NR

Academic

Fogas [22]

Abstract

Hungary

(n = 79)

MV patients

Age 69.5

Male 61 %

APACHE II 27

PPI (n = 38) H2RA (n = 41)

No molecule, route, dose or frequency described

No clear definition

Leukocytosis, elevated procalcitonin, fever, purulent ETT secretion, positive ETT microbiology, new/increased infiltrate

NR

Wee [20]

Abstract

USA

(n =129)

Critically ill patients with risk factors

Age median 72

Male NR

APACHE II 22

Pantoprazole 40 mg IV daily (n = 68)

Famotidine 20 mg IV twice daily (n = 61)

Overt bleeding with any of the following:

(1) Decrease in SBP by >20 mmHg

(2) Decrease in MAP to <65 mmHg

3. Decrease in Hb >2 g/dL and need for >1 unit of blood

NA

NR

Bhanot [38]

Abstract

India

(n = 150)

Mechanically ventilated, critically ill.

Omeprazole 40 mg PO daily (n = 50)

Ranitidine 50 mg IV four times daily (n = 50)

Sucralfate 1 gm PO four times daily (n = 50)

NR

NR

NR

Description of populations, settings, interventions, outcomes and funding sources. APACHE Acute Physiology and Chronic Health Evaluation, MV mechanically ventilated, NR not reported, GI gastrointestinal, IV intravenous, PO oral, hb hemoglobin, USFDA US Food and Drug Agency, SBP systolic blood pressure, HR heart rate, ETT endotracheal tube, WBC white blood cells, BAL, bronchiolar lavage, CFU colony-forming units, DBP diastolic blood pressure, Hct hematocrit, PPI proton pump inhibitor, H2RA histamine-2-receptor antagonist, MAP mean arterial pressure, CDC Center of disease control, NG nasogastric, NA not applicable

Risk of bias assessment

Using the Cochrane risk of bias tool, three trials were judged to be at low risk of bias, and for six trials the risk of bias was unclear (Additional file 1: Table S6). We could not evaluate the risk of bias in six trials published as abstracts [20, 23, 32–34, 38]. In total, 10 trials were judged to be at high risk of bias, primarily due to lack of or inappropriate blinding.

Assessment of quality of the evidence

We used the GRADE method [26] to assess the quality of evidence for individual outcomes. We present the details of our assessment in Table 2.
Table 2

Grading of Recommendation, Assessment, Development, and Evaluation (GRADE) evidence profile

Quality assessment

Patients, number

Effect

Quality

Studies, number

Risk of bias

Inconsistency

Indirectness

Imprecision

Other considerations

PPIs

H2RAs

Relative (95 % CI)

Absolute (95 % CI)

Clinically important bleeding

14

Seriousa

Not serious

Not serious

Not seriousb

None

13/986 (1.3 %)

39/693 (5.6 %)

RR 0.39 (0.21, 0.71)

15 fewer per 1000 (7–20 fewer)

Moderatea,b

Overt upper gastrointestinal bleeding

17

Seriousa

Not seriousc

Not serious

Not serious

None

53/1102 (4.8 %)

118/795 (14.8 %)

RR 0.48 (0.34, 0.66)

26 fewer per 1000 (17–33 fewer)

Moderatea,c

Nosocomial pneumonia

13

Seriousa

Not seriousd

Not serious

Seriouse

None

119/862 (13.8 %)

92/709 (13.0 %)

RR 1.12 (0.86, 1.46)

16 more per 1000 (18 fewer to 60 more)

Lowa,d,e

Mortality

11

Not seriousf

Not serious

Not serious

Seriouse

None

151/874 (17.3 %)

120/614 (19.5 %)

RR 1.05 (0.87, 1.27)

10 more per 1000 (25 fewer to 53 more)

Moderatee,f

ICU length of stay

7

Seriousg

Not serious

Not serious

Serioush

None

371

373

-

MD 0.58 days fewer (2.03 fewer to 0.86 more)

Lowg,h

The Guideline Development Tool was used to summarize the quality of evidence for individual outcomes based on five main domains: risk of bias, inconsistency, indirectness, imprecision, and publication bias. PPI proton pump inhibitor, H2RA histamine-2-receptor antagonist, MD mean difference, RR relative risk. aWe downgraded by one level, for risk of bias; most studies were unblinded. bAlthough the total number of events was small, we did not downgrade for imprecision. cSignificant inconsistency was not present (I 2 = 6 %). dSignificant inconsistency was not present (I 2 = 4 %). eWe downgraded by one level for imprecision; the confidence interval contains significant benefit and harm. fWe did not downgrade for risk of bias because mortality is an objective outcome that is less likely to be affected by lack of blinding in clinical trials. gWe downgraded by one level for risk of bias. hWe downgraded by one level for imprecision; the confidence interval contained significant benefit and harm

Main outcomes

A total of 14 trials enrolling 1679 patients reported clinically important GI bleeding (Fig. 2). PPI use was associated with lower risk of clinically important GI bleeding compared to H2RAs (RR 0.39; 95 % CI 0.21, 0.71; P = 0.002; I 2  = 0 %; moderate confidence). Using an assumed control event rate of 3 %, the number needed to treat (NNT) was 55 (95 % CI 42, 115). Seventeen trials enrolling 1897 patients reported overt GI bleeding (Fig. 3). Prophylaxis with PPI was associated with a lower risk of overt GI bleeding compared to H2RA (RR 0.48; 95 % CI 0.34, 0.66; P < 0.0001; I 2  = 3 %, moderate confidence). The NNT to prevent GI bleeding was 37 (95 % CI 29, 59) for an assumed control event rate of 5 %. Thirteen trials enrolling 1571 patients reported the risk of pneumonia (Fig. 4). The risk of pneumonia was similar between groups (RR 1.12; 95 % CI 0.86, 1.46; P = 0.39; I 2  = 2 %, low confidence). Eleven trials enrolling 1487 patients reported on mortality (Additional file 1: Figure S5). Mortality risk was similar between groups (RR 1.05; 95 % CI 0.87, 1.27; P = 0.61; I 2  = 0 %, moderate confidence). Seven trials enrolling 744 patients reported ICU length of stay (Additional file 1: Figure S6); ICU length of stay was not significantly different between groups (MD –0.38 days; 95 % CI –1.49, 0.74; P = 0.51; I 2  = 30 %, low confidence). None of the RCTs included reported on Clostridium difficile infection.
Fig. 2
Fig. 2

Clinically important gastrointestinal bleeding. Data from 14 trials (n = 1679 patients) are included, analyzed using the random effects model. Proton pump inhibitors (PPIs) were associated with a significantly lower risk of clinically important bleeding compared to histamine-2-receptor antagonists (H2RAs). IV Inverse Variance

Fig. 3
Fig. 3

Overt upper gastrointestinal bleeding. Data from 17 trials (n = 1897 patients) are included, analyzed using the random effects model. Proton pump inhibitors (PPIs) were associated with a significantly lower risk of overt bleeding compared to histamine-2-receptor antagonists (H2RAs). IV Inverse Variance

Fig. 4
Fig. 4

Pneumonia outcome. Data from 12 trials (n = 1471 patients) were included, analyzed using the random effects model. The risk of pneumonia was similar in both groups. PPI proton pump inhibitor, H2RA histamine-2-receptor antagonist. IV Inverse Variance

Subgroup analyses

We found no statistically significant interaction between the magnitude of effect and risk of bias, route of PPI administration, or frequency of PPI dosing. Details of the results of the subgroup analyses are in Additional file 1: Table S4 and S5.

Sensitivity analysis excluding trials published as abstracts yielded results very similar to the primary analysis (RR 0.42; 95 % CI 0.21, 0.82; P = 0.01; I 2  = 0 %) (Additional file 1: Figure S7).

Publication bias

Visual inspection of the funnel plot for clinically important GI bleeding did not suggest the presence of publication bias (Additional file 1: Figure S8). The Egger test also supported this conclusion (–0.69; 95 % CI –2.44, 0.84; P = 0.28). The Egger test was significant for overt GI bleeding, which may suggest the presence of publication bias (–0.87; 95 % CI –1.67, –0.07; P = 0.03). We did not find evidence of publication bias for the outcomes of mortality and pneumonia (Additional file 1: Figure S9 and S10).

Discussion

This systematic review demonstrated moderate quality evidence that PPIs are superior to H2RAs in reducing the risk of both clinically important and overt GI bleeding. The relative treatment effect was large (relative risk reduction of 61 % for clinically important GI bleeding), and the NNT was 55, which translates into 16 fewer bleeding events per 1000 patients. The relatively low incidence of GI bleeding currently seen in the ICU explains the apparent discrepancy between a large relative effect and small absolute effect (Table 2).

The primary concern associated with PPI use in the ICU is the potentially higher risk of infection, particularly, pneumonia and C. difficile [19], potentially a consequence of attenuation of the gastric acid protection against bacteria. Patients with achlorhydria or on long-term acid suppressive therapy have increased bacterial growth on gastric mucosal biopsy [49]. Whether this translates into increased risk of infection in critically ill patients remains unknown.

Our meta-analysis did not suggest an increased risk of pneumonia associated with PPIs rather than H2RAs. Furthermore, mortality and duration of stay in the ICU did not differ between groups. The impact of acid suppressive therapy on Clostridium difficile infection is uncertain as none of the included trials reported on this. A systematic review of 12 observational studies evaluating 2948 non-ICU patients with Clostridium difficile found an association with acid suppressive therapy (OR 1.94; 95 % CI 1.37, 2.75). This association was larger with PPI use (OR 2.05; 95 % CI 1.47, 2.85) as compared to H2RA (OR 1.47; 95 % CI 1.06, 2.05), but the difference was not statistically significant (P = 0.17) [50]. Furthermore, a retrospective cohort study that used propensity matching and included over 30,000 critically ill patients suggested that PPI use was associated with a small increase in the risk of Clostridium difficile infection in comparison to H2RA (3.4 % vs. 2.7 %; P = 0.02) [19]. As these results are limited by risk of bias associated with observational designs and imprecision, randomized trials are needed to confirm or refute these observations.

Our meta-analysis used broad eligibility criteria to enhance the generalizability of the results. Despite including a wide spectrum of critically ill patients, there was no significant heterogeneity across trials for these outcomes. Our findings suggest that PPIs are effective in preventing stress ulcer bleeding without increasing the risk of pneumonia or mortality. Nonetheless, several factors suggest cautious interpretation of these results. The quality of evidence was moderate for most outcomes; this is primarily related to risk of bias. Nine trials did not employ proper blinding of healthcare providers or outcome assessors (Additional file 1: Table S6), which may have inflated the observed treatment effect of PPIs. Furthermore, a subgroup analysis based on risk of bias (low vs. high or unclear) suggested a larger treatment effect in trials of lower quality, although the test for interaction was not significant. The outcome definitions varied across studies, which may have affected the estimate of effect.

Other factors, such as enteral nutrition, may modify the efficacy of prophylactic PPIs and H2RAs. One small RCT in critically ill patients with burns showed that enteral nutrition increased gastric blood flow [51]. No RCTs exclusively examined the effect of enteral feeding on bleeding from stress ulcers. Whether enteral feeding modifies the effect of PPIs on the risk of bleeding or pneumonia remains uncertain.

Prior meta-analyses examined the effect of PPIs compared to H2RAs for stress ulcer prophylaxis [11–14]. Our meta-analysis included more trials than other meta-analyses on this topic (19 trials enrolling 2117 patients), improving the precision of our findings. We obtained additional missing data from the authors of the original trial reports to inform the analyses, and conducted subgroup analyses to assess the robustness of the findings. Using the GRADE approach to assess our confidence in the estimates of treatment effect, the certainty of evidence was moderate for clinically important and overt upper GI bleeding, and mortality outcomes, while it was low for pneumonia and ICU length of stay outcomes. We also adhered to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guidelines [52].

Conclusions

In summary, our meta-analysis provides moderate quality evidence for clinicians and guideline groups suggesting that PPIs, when compared to H2RAs, lower the risk of clinically important and overt GI bleeding among critically ill patients, without increasing the risk of pneumonia and mortality, or ICU length of stay. The impact of these drugs on the risk of Clostridium difficile infection has yet to be examined in randomized trials in the ICU setting.

Declarations

Acknowledgements

Funding was provided by the Hamilton Chapter of the Canadian Intensive Care Foundation, the Critical Care Medicine Residency Program, and Critical Care Division Alternate Funding Plan at McMaster University.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Medicine, McMaster University, Hamilton, Canada
(2)
Department of Internal Medicine, United Arab Emirates University, Alain, United Arab Emirates
(3)
Department of Clinical Epidemiology & Biostatistics, McMaster University, Hamilton, Canada
(4)
Department of Surgery, Division of Neurosurgery, McMaster University, Hamilton, Canada
(5)
Department of Critical Care, Security Forces Hospital, Riyadh, Saudi Arabia
(6)
Department of Medicine, Alfaisal University, Riyadh, Saudi Arabia
(7)
Department of Medicine, Division of Critical Care, St Joseph’s Healthcare, 50 Charlton Avenue East, Hamilton, ON, L8N 4A6, Canada

References

  1. Skillman JJ, Silen W. Acute gastroduodenal “stress” ulceration: barrier disruption of varied pathogenesis? Gastroenterology. 1970;59(3):478–82.PubMedGoogle Scholar
  2. Shuman RB, Schuster DP, Zuckerman GR. Prophylactic therapy for stress ulcer bleeding: a reappraisal. Ann Intern Med. 1987;106(4):562–7.View ArticlePubMedGoogle Scholar
  3. Mutlu GM, Mutlu EA, Factor P. GI complications in patients receiving mechanical ventilation. Chest. 2001;119(4):1222–41.View ArticlePubMedGoogle Scholar
  4. Cook D, Heyland D, Griffith L, Cook R, Marshall J, Pagliarello J. Risk factors for clinically important upper gastrointestinal bleeding in patients requiring mechanical ventilation. Canadian Critical Care Trials Group. Crit Care Med. 1999;27(12):2812.View ArticlePubMedGoogle Scholar
  5. D’Ancona G, Baillot R, Poirier B, et al. Determinants of gastrointestinal complications in cardiac surgery. Tex Heart Inst J. 2003;30(4):280–5.PubMedPubMed CentralGoogle Scholar
  6. Faisy C, Guerot E, Diehl JL, Iftimovici E, Fagon JY. Clinically significant gastrointestinal bleeding in critically ill patients with and without stress-ulcer prophylaxis. Intensive Care Med. 2003;29(8):1306–13.View ArticlePubMedGoogle Scholar
  7. Krag M, Perner A, Wetterslev J, et al. Prevalence and outcome of gastrointestinal bleeding and use of acid suppressants in acutely ill adult intensive care patients. Intensive Care Med. 2015;1-13.Google Scholar
  8. Cook DJ, Griffith LE, Walter SD, et al. The attributable mortality and length of intensive care unit stay of clinically important gastrointestinal bleeding in critically ill patients. Crit Care. 2001;5(6):368–75.View ArticlePubMedPubMed CentralGoogle Scholar
  9. Krag M, Perner A, Wetterslev J, Wise MP, Hylander MM. Stress ulcer prophylaxis versus placebo or no prophylaxis in critically ill patients: A systematic review of randomised clinical trials with meta-analysis and trial sequential analysis. Intensive Care Med. 2014;40(1):11–22.View ArticlePubMedGoogle Scholar
  10. Reilly J, Fennerty MB. Stress ulcer prophylaxis: The prevention of gastrointestinal bleeding and the development of nosocomial infections in critically ill patients. J Pharm Pract. 1998;11(6):418–36.View ArticleGoogle Scholar
  11. Pongprasobchai S, Kridkratoke S, Nopmaneejumruslers C. Proton pump inhibitors for the prevention of stress-related mucosal disease in critically-ill patients: a meta-analysis. J Med Assoc Thai. 2009;92(5):632–7.PubMedGoogle Scholar
  12. Alhazzani W, Alenezi F, Jaeschke RZ, Moayyedi P, Cook DJ. Proton pump inhibitors versus histamine 2 receptor antagonists for stress ulcer prophylaxis in critically ill patients: A systematic review and meta-analysis. Crit Care Med. 2013;41(3):693–705.View ArticlePubMedGoogle Scholar
  13. Barkun AN, Bardou M, Pham CQ, Martel M. Proton pump inhibitors vs. histamine 2 receptor antagonists for stress-related mucosal bleeding prophylaxis in critically ill patients: a meta-analysis. Am J Gastroenterol. 2012;107(4):507–20.View ArticlePubMedGoogle Scholar
  14. Lin PC, Chang CH, Hsu PI, Tseng PL, Huang YB. The efficacy and safety of proton pump inhibitors vs histamine-2 receptor antagonists for stress ulcer bleeding prophylaxis among critical care patients: a meta-analysis. Crit Care Med. 2010;38(4):1197–205.View ArticlePubMedGoogle Scholar
  15. Dellinger RP, Levy MM, Rhodes A, et al. Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock: 2012. Crit Care Med. 2013;41(2):580–637.View ArticlePubMedGoogle Scholar
  16. Barletta JF, Kanji S, MacLaren R, Lat I, Erstad BL. American-Canadian consortium for Intensive care Drug utilization I. Pharmacoepidemiology of stress ulcer prophylaxis in the United States and Canada. J Crit Care. 2014;29(6):955–60.View ArticlePubMedGoogle Scholar
  17. Eastwood GM, Litton E, Bellomo R, et al. Opinions and practice of stress ulcer prophylaxis in Australian and New Zealand intensive care units. Crit Care Resusc. 2014;16(3):170–4.PubMedGoogle Scholar
  18. Krag M, Perner A, Wetterslev J, et al. Stress ulcer prophylaxis in the intensive care unit: an international survey of 97 units in 11 countries. Acta Anaesthesiol Scand. 2015;59(5):576–85.View ArticlePubMedGoogle Scholar
  19. MacLaren R, Reynolds PM, Allen RR. Histamine-2 receptor antagonists vs proton pump inhibitors on gastrointestinal tract hemorrhage and infectious complications in the intensive care unit. JAMA Intern Med. 2014;174(4):564–74.View ArticlePubMedGoogle Scholar
  20. Wee B, Liu CH, Cohen H, Kravchuk S, Reddy K, Mukherji R. IV Famotidine vs. IV Pantoprazole for Stress Ulcer Prevention in the ICU: A Prospective Study. In: Parrilo JE, editor. GI/Nutrition 1. The 43rd Critical Care Congress; 2014 Jan 9-13; San Francisco, California, USA. Critical Care Medicine. 2013;41(12):637.Google Scholar
  21. Bhanot RD. Nosocomial pneumonia in mechanically ventilated patients receiving ranitidine, omeprazole or sucralfate as stress ulcer prophylaxis. Am J Respir Crit Care Med. 2010;181:A6039 (1 MeetingAbstracts).Google Scholar
  22. Bashar FR, Manuchehrian N, Mahmoudabadi M, Hajiesmaeili MR, Torabian S. Effects of ranitidine and pantoprazole on Ventilator- associated Pneumonia: A randomized double-blind clinical trial. Tanaffos. 2013;12(2):16–21.PubMedPubMed CentralGoogle Scholar
  23. Fogas JF, Kiss KK, Gyura FG, Tobias ZT, Molnar ZM. Effects of proton pump inhibitor versus H2-receptor antagonist stress ulcer prophylaxis on ventilator-associated pneumonia: A pilot study. Crit Care (London, England). 2013;17:S150–1.Google Scholar
  24. Lee TH, Hung FM, Yang LH. Comparison of the efficacy of esomeprazole and famotidine against stress ulcers in a neurosurgical intensive care unit. Advances in Digestive Medicine. 2014;1(2):50–3.View ArticleGoogle Scholar
  25. Liu BL, Li B, Zhang X, et al. A randomized controlled study comparing omeprazole and cimetidine for the prophylaxis of stress-related upper gastrointestinal bleeding in patients with intracerebral hemorrhage: Clinical article. J Neurosurg. 2013;118(1):115–20.View ArticlePubMedGoogle Scholar
  26. Guyatt GH, Oxman AD, Vist GE, et al. GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ. 2008;336(7650):924–6.View ArticlePubMedPubMed CentralGoogle Scholar
  27. Higgins JP, Altman DG, Gotzsche PC, et al. The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ. 2011;343:d5928.View ArticlePubMedPubMed CentralGoogle Scholar
  28. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–88.View ArticlePubMedGoogle Scholar
  29. Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327(7414):557–60.View ArticlePubMedPubMed CentralGoogle Scholar
  30. Schünemann HJ, Oxman AD, Vist GE, Higgins JPT, Deeks JJ, Glasziou P, Guyatt GH. Chapter 12: Interpreting results and drawing conclusions. In: Higgins JPT, Green S (editors), Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 (updated March 2011). The Cochrane Collaboration, 2011. Available from www.cochrane-handbook.org.
  31. Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315(7109):629–34.View ArticlePubMedPubMed CentralGoogle Scholar
  32. Kotlyanskaya A, Cohen H, Luka B, Mukherji R, Shukla M, Vajinder T. A comparison of lansoprazole disintegrating tablet, lansoprazole suspension or ranitidine for stress ulcer prophylaxis in critically ill patients. Crit Care Med. 2007;35(12):A194.Google Scholar
  33. Phillips JO, Metzler MH, Huckfeldt RE, Olsen K. A multicenter, prospective, randomized clinical trial of continuous infusion i.v. ranitidine vs. omeprazole suspension in the prophylaxis of stress ulcers. Crit Care Med. 1998;26(1):101A.View ArticleGoogle Scholar
  34. Fink M, Karlstadt RG, Maroko RT, Field B. Intravenous pantoprazole (IVP) and continuous infusion cimetidine (C) prevent upper gastrointestinal bleeding (UGIB) regardless of APSII score (APACHE II) in high risk intensive care unit (ICU) patients. Gastroenterology. 2003;124(4):A625-A626.Google Scholar
  35. Somberg L, Morris Jr J, Fantus R, et al. Intermittent intravenous pantoprazole and continuous cimetidine infusion: effect on gastric pH control in critically ill patients at risk of developing stress-related mucosal disease. J Trauma. 2008;64(5):1202–10.View ArticlePubMedGoogle Scholar
  36. Morris JA. Intermittent intravenous pantoprazole rapidly achieves and maintains gastric ph > =4 compared with continuous infusion h2-receptor antagonist in intensive care unit (ICU) patients. Crit Care Med. 2002;30(12):A34.View ArticleGoogle Scholar
  37. Chacko A, Peter S, Nair A. Stress Ulcer Prophylaxis: A Randomised Controlled Clinical Trial with Oral Omeprazole and Ranitidine. Indian Journal of Gastroenterology. 1996;15(supp):A29.Google Scholar
  38. Bhanot RD. Nosocomial pneumonia in mechanically ventilated patients receiving ranitidine, omeprazole or sucralfate as stress ulcer prophylaxis [abstract]. Am J Respir Crit Care Med. 2010;181(supp):A6039.Google Scholar
  39. Conrad SA, Gabrielli A, Margolis B, et al. Randomized, double-blind comparison of immediate-release omeprazole oral suspension versus intravenous cimetidine for the prevention of upper gastrointestinal bleeding in critically ill patients. Crit Care Med. 2005;33(4):760–5.View ArticlePubMedGoogle Scholar
  40. De Azevedo JRA, Soares MDGA, Silva GAE, De Lima Palacio G. Prevention of stress ulcer bleeding in high risk patients. Comparison of three drugs. [Portuguese]. GED - Gastrenterologia Endoscopia Digestiva. 2000;19(6):239–44.Google Scholar
  41. Hata M, Shiono M, Sekino H, et al. Prospective randomized trial for optimal prophylactic treatment of the upper gastrointestinal complications after open heart surgery. Circ J. 2005;69(3):331–4.View ArticlePubMedGoogle Scholar
  42. Kantorova I, Svoboda P, Scheer P, et al. Stress ulcer prophylaxis in critically ill patients: a randomized controlled trial. Hepatogastroenterology. 2004;51(57):757–61.PubMedGoogle Scholar
  43. Levy MJ, Seelig CB, Robinson NJ, Ranney JE. Comparison of omeprazole and ranitidine for stress ulcer prophylaxis. Dig Dis Sci. 1997;42(6):1255–9.View ArticlePubMedGoogle Scholar
  44. Pan X, Zhang W, Li Z, et al. The preventive effects of rabeprazole on upper gastrointestinal tract hemorrhage in patients with severe acute pancreatitis. [Chinese]. Chin J Gastroenterol. 2004;9(1):30–2.Google Scholar
  45. Powell H, Morgan M, Li SK, Baron JH. Inhibition of gastric acid secretion in the intensive care unit after coronary artery bypass graft. A pilot control study of intravenous omeprazole by bolus and infusion, ranitidine and placebo. Theor Surg. 1993;8(3):125–30.Google Scholar
  46. Risaliti A, Terrosu G, Uzzau A, et al. Intravenous omeprazole vs ranitidine in the prophylaxis of stress ulcers. [Italian]. Acta Chir Ital. 1993;49(4):397–401.Google Scholar
  47. Solouki M, Mar’ashian SM, Koochak M, Nasiri A, Mokhtari M, Amirpour A. Ventilator-associated pneumonia among ICU patients receiving mechanical ventilation and prophylaxis of gastrointestinal bleeding. Iran J Clin Infect Dis. 2009;4(3):177–80.Google Scholar
  48. Solouki M, Marashian SM, Kouchak M, Mokhtari M, Nasiri E. Comparison between the preventive effects of ranitidine and omeprazole on upper gastrointestinal bleeding among ICU patients. Tanaffos. 2009;8(4):37–42.Google Scholar
  49. Williams C, McColl KE. Review article: proton pump inhibitors and bacterial overgrowth. Aliment Pharmacol Ther. 2006;23(1):3–10.View ArticlePubMedGoogle Scholar
  50. Leonard J, Marshall JK, Moayyedi P. Systematic review of the risk of enteric infection in patients taking acid suppression. Am J Gastroenterol. 2007;102(9):2047–56. quiz 2057.View ArticlePubMedGoogle Scholar
  51. Yan H, Peng X, Huang Y, Zhao M, Li F, Wang P. Effects of early enteral arginine supplementation on resuscitation of severe burn patients. Burns. 2007;33(2):179–84.View ArticlePubMedGoogle Scholar
  52. Moher D, Shamseer L, Clarke M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev. 2015;4:1.View ArticlePubMedPubMed CentralGoogle Scholar

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