Author/Authors :
Morrisette Matthew Joseph نويسنده Department of Pharmacy, Carolinas Medical Center,
Charlotte, United States of America , Hammer John Michael نويسنده Department of Pharmacy, Carolinas Medical Center,
Charlotte, United States of America , Anderson William Edward نويسنده Department of Biostatistics, Carolinas Medical Center,
Charlotte, United States of America , Norton Harry James نويسنده Department of Biostatistics, Carolinas Medical Center,
Charlotte, United States of America , Green Michael Brian نويسنده Department of Pulmonary and Critical Care, Carolinas
Medical Center, Charlotte, United States of America , Gesin Gail نويسنده Department of Pharmacy, Carolinas Medical Center,
Charlotte, United States of America
Abstract :
Background: Lack of well-supported evidence clearly defining one
agent as superior to the other for use in stress ulcer prophylaxis (SUP)
has led to an array of treatment strategies. Studies comparing
histamine-2 receptor antagonists (H2RAs) and proton pump inhibitors
(PPIs) have shown H2RAs to be non-inferior to PPIs at preventing
clinically significant gastric bleeding. This, in addition to the
decreased cost associated with H2RAs, has led to the adoption of H2RAs
as the preferred agent for SUP at our institution. Objectives: To
evaluate the impact of developing a guideline and removing PPIs from
computerized order entry PowerPlans on PPI prescribing for SUP in
critically ill patients. Patients and Methods: Members of the critical
care service developed a guideline to direct SUP and removed
pantoprazole from two critical care admission PowerPlans. In this
interventional study with a historical control, adult patients admitted
to the medical or surgical-trauma ICU and prescribed a PPI were
evaluated during two time periods before and after the interventions.
Patients were excluded if they were receiving a PPI for a reason other
than SUP. Patients were assessed daily for an indication for SUP. These
included mechanical ventilation, high dose steroids, and coagulopathy.
Results: A total of 92 and 60 patients were included in the pre- and
post-intervention groups, respectively. PPI use for SUP was reduced from
38% in the pre-intervention group to 15.6% in the post-intervention
group (P < 0.0001). PPI days adjusted for LOS were not different
between the pre- and post-intervention groups (84% vs 86%, P = 0.5909).
Of the total PPI days, 52.4% (95% CI 48.8 - 56.1) were classified as
inappropriate because there was no indication, while the remaining 47.6%
(95% CI 43.9 - 51.2) had an indication but should have received a H2RA.
The total cost associated with guideline non-adherence was $1802.
Conclusions: Our multifaceted intervention reduced the number of days in
which a PPI was prescribed for SUP in the overall ICU population;
however, it did not impact the duration of PPI therapy. Patients either
had no indication for SUP, or had an indication where less costly H2RAs
could have been used. Additional opportunity exists to improve
cost-effective prescribing of SUP for critically ill patients.