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Background Proton pump inhibitors (PPI) are frequently prescribed for prophylaxis of nosocomial upper gastrointestinal bleeding (UGIB). Some inpatients receiving PPI may be without risk factors for nosocomial UGIB, and PPI may be continued unnecessarily at hospital discharge. Aim To assess the impact of standardized guidelines on PPI prescribing practices. Methods: Guidelines for PPI use were implemented on the medical service at a tertiary center. We reviewed PPI use among inpatient admissions during the month prior to implementation of guidelines then prospectively evaluated PPI use among admissions during the month following implementation of guidelines. Results 49% of patients (458/942) received PPI while inpatient, and 41% of patients (387/942) were prescribed PPI at discharge. Univariate predictors of inpatient PPI use included age, length of stay, history of GERD or UGIB, outpatient PPI use, outpatient aspirin use, and outpatient glucocorticoid use. Among patients not on outpatient PPI at admission, implementation of guidelines resulted in lower rates of inpatient PPI use (27% pre- vs 16% post-guidelines, P=0.001) and PPI prescription at discharge (16% pre- vs. 10% post-guidelines, P=0.03). Conclusions Introduction of standardized guidelines resulted in lower rates of PPI use among a subset of hospital inpatients and reduced the rate of PPI prescriptions at hospital discharge.
Background Proton pump inhibitors (PPI) are frequently prescribed for prophylaxis of nosocomial upper gastrointestinal bleeding (UGIB). Some inpatients receiving PPI may be without risk factors for nosocomial UGIB, and PPI may be continued unnecessarily at hospital discharge. Aim To assess the impact of standardized guidelines on PPI prescribing practices. Methods: Guidelines for PPI use were implemented on the medical service at a tertiary center. We reviewed PPI use among inpatient admissions during the month prior to implementation of guidelines then prospectively evaluated PPI use among admissions during the month following implementation of guidelines. Results 49% of patients (458/942) received PPI while inpatient, and 41% of patients (387/942) were prescribed PPI at discharge. Univariate predictors of inpatient PPI use included age, length of stay, history of GERD or UGIB, outpatient PPI use, outpatient aspirin use, and outpatient glucocorticoid use. Among patients not on outpatient PPI at admission, implementation of guidelines resulted in lower rates of inpatient PPI use (27% pre- vs 16% post-guidelines, P=0.001) and PPI prescription at discharge (16% pre- vs. 10% post-guidelines, P=0.03). Conclusions Introduction of standardized guidelines resulted in lower rates of PPI use among a subset of hospital inpatients and reduced the rate of PPI prescriptions at hospital discharge.
Background The incidence of community-acquired Clostridium difficile (CACD) is increasing in the US. Many CACD infections occur in the elderly who are predisposed to poor outcomes. We aimed to describe the epidemiology and outcomes of CACD in a nationally representative sample of Medicare beneficiaries. Study Design We queried a 5% random sample of Medicare beneficiaries (2009–2011 Part A inpatient and Part D prescription drug claims, N=864,604) for any hospital admission with a primary ICD-9 diagnosis code for C. difficile (008.45). We examined patient sociodemographic and clinical characteristics, pre-admission exposure to oral antibiotics, prior treatment with oral vancomycin or metronidazole, inpatient outcomes (colectomy, ICU stay, length of stay, mortality), and subsequent admissions for C. difficile. Results A total of 1566 (0.18%) patients were admitted with CACD. Of these, 889(56.8%) received oral antibiotics within 90 days of admission. Few were being treated with oral metronidazole (N=123, 7.8%) or vancomycin (N=13, 0.8%) at the time of admission. While 223(14%) patients required ICU admission, few (N=15, 1%) underwent colectomy. Hospital mortality was 9%. Median length of stay (LOS) among survivors was 5 days (IQR 3–8). One- fifth of survivors were re-admitted with C. difficile with a median follow up time of 393 days (IQR 129–769). Conclusions Nearly half of Medicare beneficiaries admitted with CACD have no recent antibiotic exposure. High mortality and re-admission rates suggest that the burden of C. difficile on patients and the healthcare system will increase as the US population ages. Additional efforts at primary prevention and eradication may be warranted.
The Gram-positive, spore-forming bacterium, Clostridioides difficile is the leading cause of healthcare-associated infections in the United States, although it also causes a significant number of community-acquired infections. C. difficile infections, which range in severity from mild diarrhea to toxic megacolon, cost more to treat than matched infections, with an annual treatment cost of approximately $6 billion for almost half-a-million infections. These high–treatment costs are due to the high rates of C. difficile disease recurrence (>20%) and necessity for special disinfection measures. These complications arise in part because C. difficile makes metabolically dormant spores, which are the major infectious particle of this obligate anaerobe. These seemingly inanimate life forms are inert to antibiotics, resistant to commonly used disinfectants, readily disseminated, and capable of surviving in the environment for a long period of time. However, upon sensing specific bile salts in the vertebrate gut, C. difficile spores transform back into the vegetative cells that are responsible for causing disease. This review discusses how spores are ideal vectors for disease transmission and how antibiotics modulate this process. We also describe the resistance properties of spores and how they create challenges eradicating spores, as well as promote their spread. Lastly, environmental reservoirs of C. difficile spores and strategies for destroying them particularly in health care environments will be discussed.
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