Index
Module 14 • Preventive Care
Supportive & Preventive Medicine
38%
Data Tables
Supportive & Preventive Medicine
Megan Feeney ~4 min read Module 14 of 20
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Supportive and Preventive Medicine

Meta-analyses have failed to show an association between H2RAs and PPIs on the risk of pneumonia

(Crit Care Med 2013;41:693-705; Am J Gastroenterol 2012;107:507-20; Crit Care Med 2010;38:1197-

205); a network meta-analysis conducted and published with the most recent clinical practice

guidelines further supports no association between PPIs and risk of pneumonia (Crit Care Med.
2016;44(10):1842-1850; Crit Care Med. 2017;45(7):1121-1129; N Engl J Med. 2018;379(23):2199-2208).

However, patients concurrently receiving enteral nutrition and SUP were found to be at increased

risk of pneumonia in a recent systematic review and meta-analysis (Crit Care. 2018;22(1):20).
d.In two large pharmacoepidemiologic cohorts, an increase in the propensity-adjusted odds of

pneumonia occurred with PPIs compared with H2RAs (OR 1.2; CI, 1.03โ€“1.41) in mechanically

ventilated patients (JAMA Intern Med 2014;174:564-7) and in patients admitted for cardiac surgery

after propensity matching (OR 1.19; CI, 1.03โ€“1.38) (BMJ 2013;347:f5416).

Many of the trials included in these analyses had varying definitions of pneumonia.

5

CDI

A pharmacoepidemiologic cohort study found that CDI rates were significantly higher with PPIs

than with H2RAs (3.8% vs. 2.2%; p<0.001) (JAMA Intern Med 2014;174:564-7).

A large retrospective study found PPI use to be an independent risk factor for developing CDI in

medical ICU patients (OR 3.11; 95% CI, 1.11โ€“8.74) (J Crit Care 2014;29:696).

No prospective trials have been large enough to evaluate the risk of CDI in ICU patients.

d.Many published trials have different definitions of CDI, unclear association of antisecretory therapy

initiation and CDI diagnosis, and variable infection control practices.

6

In the SUP-ICU trial, there was no difference in infectious adverse events (new-onset pneumonia or

CDI).

7

There also were no differences in infectious adverse events (ventilator-associated pneumonia [VAP] in

ICU, CDI in hospital) between the pantoprazole and placebo groups in the REVISE trial.

8

SUP duration should be evaluated daily, and SUP should be discontinued as long as no risk factors are

present.

H.Pharmacoeconomics
1

According to the landmark trial comparing H2RAs with sucralfate, H2RAs may be more cost-effective

because of a reduced incidence of bleeding without an increase in pneumonia rates (N Engl J Med

1998;338:791-7).

2Cost-effectiveness models have compared H2RAs with PPIs with respect to clinically important

bleeding and adverse effects (VAP and CDI).

Use of PPI therapy for SUP resulted in a $1250 net cost savings per patient compared with

H2RAs. Univariate sensitivity analysis showed that PPI therapy was not as cost-effective when the

probability of VAP rates was altered (Value Health 2013;16:14-22).

Use of H2RA therapy for SUP resulted in a $1095 net cost savings compared with PPIs. Univariate

sensitivity analysis showed that assumptions of pneumonia and bleeding rates were the primary

drivers of incremental costs (Crit Care Med 2014;42:809-15).
3

Initiating SUP in patients at risk and appropriately discontinuing SUP when a patient no longer has any

of the risk factors for stress-related bleeding is the best practice for cost minimization.

I.

Guideline Recommendations

1

In 1999, the first guideline from the American Society of Health-System Pharmacists was published

(Am J Health Syst Pharm 1999;56:347-79). The guideline recommended that institutions decide on

H2RAs, antacids, or sucralfate according to safety profile, costs, and ease of administration.

2In 2008, the Eastern Association for the Surgery of Trauma published a guideline recommending

cytoprotective agents, H2RAs, or PPIs; antacids were not recommended (www.east.org).

3
In 2014, the Danish Society of Intensive Care Medicine and the Danish Society of Anaesthesiology
and Intensive Care Medicine published guidelines suggesting PPIs as the preferred agent (Dan Med J

2014;61:C4811).

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