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Clostridium difficile-associated diarrhea in a tertiary care medical center.

Outbreaks of Clostridium difficile--associated diarrhea (CDAD) have been reported in acute care as well as long-term care facilities (1, 2). Disruption of the normal gut flora allows colonization with C. difficile (3). C. difficile colonization in adult patients may increase by 10% to 30% during hospitalization, but not all patients will develop disease. Known risk factors associated with CDAD development include prior exposure to antimicrobials, gastrointestinal (GI) surgery, feeding tubes, chemotherapy, environmental exposure, advanced age, severity of comorbid conditions, and GI stimulants, stool softeners, and enemas (1, 2, 4, 5). Although the strongest evidence with antimicrobial exposure exists with clindamycin, penicillins, and cephalosporins (4-11), reports have implicated fluoroquinolone use as a potential risk factor in the development of CDAD (2, 11-20). Proton pump inhibitors (PPIs) are another pharmacologic class suggested as a risk factor in the development of CDAD (21, 22).

Hillcrest Medical Center is a licensed 557-bed tertiary care hospital located in northeast Oklahoma. This institution had experienced an apparent increase in CDAD cases over a 2-year period (years 2001-2003) with no defined cause, although a correlation with a formulary change from levofloxacin to moxifloxacin had been postulated. In addition, intravenous PPI therapy became available during this time period. The primary objective of this study was to evaluate the relationship of CDAD with levofloxacin or moxifloxacin use in acutely ill patients. Secondary study objectives included evaluating the relationship between CDAD and PPI use in acutely ill patients and describing the treatment regimens and outcomes of CDAD patients.


Study design

This study was conducted in the general medical wards and intensive care units (ICUs) at Hillcrest Medical Center. A retrospective chart review was conducted in patients with CDAD or at risk for CDAD in acute care areas who were admitted between August 1, 2001, and August 31, 2003. Levofloxacin was the formulary fluoroquinolone from August 2001 to June 2002, and moxifloxacin was utilized from July 2002 to the end of the study analysis. Patients were excluded from participation if they were discharged from the hospital in <72 hours, were <18 or >89 years of age, had a previous CDAD diagnosis, showed symptoms within rather than after 72 hours of hospitalization, were treated in nonacute care areas, or did not have a chart available from medical records. This study was approved by the institutional review boards of the University of Oklahoma Health Sciences Center and Hillcrest Medical Center. Medical charts included in the study were identified using microbiological data (identification of C. difficile toxin A/B during the study period; Wompole[TM] C. Diff QuikChek Complete[TM], Inverness Medical, Princeton, NJ) and admission data.

A retrospective case-control study design was used. Cases included patients with acute onset of loose bowel movements persisting for [greater than or equal to] 2 days who tested positive for C. difficile toxin A and/or toxin B. The date of positive toxin test was defined as the date of diagnosis. For each case patient with CDAD, two control patients were matched for age (within 5 years), unit of admission, and month of admission. Controls had to have a minimum length of stay of 3 days. Data from a single case of CDAD for each patient were included in the study analysis. Data collected included patient age, gender, race, the presence of comorbidities, alcohol abuse or current use of cigarettes as identified in the social history, patient location at time of CDAD diagnosis, and diagnosis at admission. The following variables were documented and assessed as risk factors associated with exposure before the development of CDAD: recent hospital admission within the previous 90 days, admission to the ICU, length of hospital stay prior to CDAD diagnosis, total hospital length of stay, GI procedure or surgery within 60 days of illness or during admission, previous antimicrobial use (e.g., fluoroquinolones, vancomycin, clindamycin, penicillins, cephalosporins, metronidazole), duration of antimicrobial treatment, other medications (chemotherapy, immunosuppressives, PPIs, histamine-2 receptor antagonists [H2RAs]), administration of enteral or parenteral nutrition, and presence of a nasogastric or nasotracheal tube. Data were recorded until the patient was discharged from the hospital, transferred to a long-term care facility, or died.

Statistical analysis

Statistical analysis was performed using SAS software, version 9.1 (SAS Institute, Cary, NC) (23). Univariate analysis was performed separately for each of the variables. Variables with a P value of [less than or equal to] 0.2 in the univariate analysis were included in a conditional multiple logistic regression model, as were the indicator variables for prior exposure to moxifloxacin and levofloxacin since these were the primary variables of interest. A manual backward selection process was used. Risk factors were checked for confounding and colinearity. Confounders were included in multivariate models if covariate inclusion changed the coefficient of any statistically significant variable in the logistic regression model by 10% or greater. The odds ratios for prior exposure to moxifloxacin and levofloxacin were evaluated using a Z test comparing parameter estimates. All tests were two tailed, and a P value of [less than or equal to] 0.05 was considered significant in the multivariate model.


Based on microbiological data, 302 patients were identified as positive for C. difficile toxin A or B during the study period. Of these patients, 46 were excluded for prior C. difficile infection, 26 patients were symptomatic within 72 hours of hospitalization, 102 patients were admitted to the rehabilitation or long-term care units, 27 patients did not meet the age requirements, and 30 patients were unable to be matched to the two required control patients. Data were collected and analyzed for 71 case and 142 control patients.

Only three patient characteristics were significantly different between the case and control groups: recent hospitalization, GI procedure in the last 60 days, and GI procedure in the hospital (Table 1). The most commonly performed GI procedures for both groups included colonoscopy, exploratory laparotomy, esophagogastroduodenoscopy, and percutaneous endoscopic gastrostomy tube placement. The use of several types of medication was associated with CDAD, but PPIs and H2RAs were not among them (Table 2).

In the logistic regression model controlling for hospital stay within the previous 3 months and Charlson Comorbidity Index, six variables were found to increase the risk of CDAD (Table 3). The risk of developing CDAD after moxifloxacin or levofloxacin exposure was not significantly different. The case patients who received levofloxacin therapy received it primarily on an outpatient basis where a majority of patients who received moxifloxacin were treated on an inpatient basis. Treatment of the CDAD episode for case patients included metronidazole therapy in 89% and withdrawal of the suspected causative agent in 11%. As shown in Table 4, patients who developed CDAD had longer lengths of stay for both the ICU and total hospitalization. Mortality was similar in the case and control patients.


Our study suggests that there is an increased risk of CDAD after exposure to moxifloxacin or levofloxacin in patients who develop symptoms and test positive for C. difficile toxin A or B after 72 hours of admission to the hospital. No statistically significant difference in risk of CDAD development was identified between moxifloxacin exposure and levofloxacin exposure. The hypothesis that moxifloxacin could increase CDAD rates as compared to levofloxacin is due to its greater propensity to affect anaerobic organisms (24). Several case reports and reviews have identified this potential risk (25). Our findings are similar to a recent case-control study of outpatients that found comparable risks of hospitalization for CDAD with gatifloxacin, moxifloxacin, and levofloxacin (26). Two studies have also postulated an increase in CDAD related to a change in formulary fluoroquinolone, although only one of these studies was able to control the outbreak by switching back to the original fluoroquinolone (2, 27). A large retrospective case-control study completed within the Veterans Administration (VA) documented that the increased CDAD rates observed were not associated with fluoroquinolone formulary change to gatifloxacin but with seasonal variation in CDAD rates (28). Another case-control study in the VA system confirmed that an increase in CDAD rates was not associated with the addition of gatifloxacin to the formulary (29). A prospective study of nosocomial CDAD in several Canadian institutions found an increased risk with ciprofloxacin, levofloxacin, and gatifloxacin in a multivariate model (30). Continuing research in this area suggests that fluoroquinolones in general are risk factors for CDAD development (11, 31-33).

The effect of acid suppressive therapy on rates of CDAD has recently been debated (34). In our study, no association was identified between PPIs or H2RAs and increased risk of CDAD. An explanation for this in our study may be the low number of patients using these agents in the outpatient setting and the possibility that increased risk may be related to prolonged use. Several other studies have found no link between acid suppressive therapy and CDAD, including a VA study (28), a recent case-control trial of community-dwelling outpatients (35), a study of hospitalized patients (32), and a prospective study in several institutions in Canada (30). In contrast, a large community-based case-control trial found that the use of acid suppressants, especially PPIs, as well as nonsteroidal anti-inflammatory agents was associated with an increased risk for development of CDAD (36), and a retrospective case-control study in Kansas identified an increased risk of CDAD with exposure to PPI therapy (37). In all, the data remain inconclusive but confirm that PPIs should be screened for inappropriate use and discontinued in those situations to avoid potential adverse sequelae (38).

An interesting finding in our study was the increased risk of CDAD after GI procedures completed within the previous 60 days. The ability to associate the development of CDAD with the procedure itself versus the agents used prior to the procedures (i.e., electrolyte preparation solutions or topical antimicrobial agents) is limited by the lack of outpatient information. A proportion of patients in this study also underwent inpatient GI procedures, raising the question of whether these patients had inflammatory bowel disease that was previously undiagnosed and not captured due to study design. In prior studies, there appears to be a link with preexisting intestinal conditions or procedures and CDAD development (28, 39). The increased risk of CDAD with laxative exposure is not a new finding (4).

The increased risk of CDAD with imipenem/cilastatin found in our study is supported by evidence from other trials in patients with immunosuppression. A significant increase in CDAD occurred with imipenem/cilastatin compared with clinafloxacin for empiric treatment of febrile neutropenia (40). A similar finding of increased CDAD in neutropenic patients was found with imipenem and vancomycin compared with cefoperazone-sulbactam and vancomycin therapy for suspected or documented infections (41). Compared with ceftazidime, use of imipenem in febrile neutropenic patients was associated with greater gastrointestinal toxicity, including CDAD and nausea and vomiting (42). A recent case-control study of CDAD in hospitalized patients also identified that imipenem/cilastatin was associated with increased rates of CDAD (43).

The identification of those patients most at risk for CDAD is paramount in the prevention and treatment of this disease. Scoring models for CDAD have been developed to identify those patients who may be at risk (44, 45). The Waterlow score, used for identifying the risk of developing pressure ulcers, has also been linked to the risk of CDAD (44). Also utilized is the clinical risk scoring model, which has four variables (age, hemodialysis, surgical admission status, and ICU length of stay) and identifies those patients at risk for CDAD (45). These scoring models, when used appropriately, may help guide physicians when prescribing broad-spectrum antimicrobial therapy, ordering GI procedures, and implementing preventative CDAD procedures.

Due to the design of this study, several major limitations must be addressed. This review was conducted at a single institution. Our study focused on patients who may have acquired CDAD after hospitalization in an effort to capture inpatient exposures to medications or other risk factors, which limits the ability to generalize these results to other patient populations. Due to the retrospective nature of the study, the agents selected for treatment for the initial suspected infection or CDAD could not be controlled. In addition, the complete duration of therapy of the various antimicrobial, immunosuppressive, laxative, and acid-reducing agents could not be specified with the current design, as only the inpatient duration could be captured. While patients with CDAD receive isolation control including handwashing, gowning, and gloving as standard procedures in this institution, these variables are not routinely documented in the chart once isolation procedures are ordered. Another limitation to the study is the small number of patients who received moxifloxacin and levofloxacin during the study period, thus limiting the power of the study. This reduction in power may have resulted in the inability to find a significant difference between fluoroquinolone exposures. The number of potential patients was greatly reduced by excluding patients who were symptomatic within the initial 72 hours of hospitalization or who had previous CDAD and the inability to match case patients with controls meeting the specified criteria. The strains of C. difficile were not sent for epidemiologic typing to identify outbreak isolates, nor was antibiotic susceptibility testing completed for any of the isolates. This study is also limited because there could have been some changes in practice or differences in risk of CDAD due to other factors (seasonal or random differences in outbreaks) that could not be controlled.

In conclusion, in patients with CDAD identified after at least 72 hours of hospitalization, an increased risk is present after exposure to levofloxacin, moxifloxacin, imipenem/cilastatin, laxative use, immunosuppressive use, and GI procedures within the previous 60 days. The risk of CDAD exposure was not significantly different between moxifloxacin or levofloxacin exposure. Exposure to PPIs or H2RAs did not increase the risk of CDAD development.

(1.) Gerding DN, Johnson S, Peterson LR, Mulligan ME, Silva J Jr. Clostridium difficile-associated diarrhea and colitis. Infect Control Hosp Epidemiol 1995;16(8):459-477.

(2.) Gaynes R, Rimland D, Killum E, Lowery HK, Johnson TM 2nd, Killgore G, Tenover FC. Outbreak of Clostridium difficile infection in a long-term care facility: association with gatifloxacin use. Clin Infect Dis 2004;38(5):640-645.

(3.) Groschel DHM. Clostridium difficile infection. Crit Rev Clin Lab Sci 1996;33(3):203-245.

(4.) McFarland LV, Surawicz CM, Stamm WE. Risk factors for Clostridium difficile carriage and C. difficile-associated diarrhea in a cohort of hospitalized patients. J Infect Dis 1990;162(3):678-684.

(5.) Owens RC Jr, Donskey CJ, Gaynes RP, Loo VG, Muto CA. Antimicrobialassociated risk factors for Clostridium difficile infection. Clin Infect Dis 2008;46(Suppl 1):S19-S31.

(6.) Gerding DN, Olson MM, Peterson LR, Teasley DG, Gebhard RL,

Schwartz ML, Lee JT Jr. Clostridium difficile-associated diarrhea and colitis in adults. A prospective case-controlled epidemiologic study. Arch Intern Med 1986;146(1):95-100.

(7.) Tedesco FJ, Barton RW, Alpers DH. Clindamycin-associated colitis. A prospective study. Ann Intern Med 1974;81(4):429-433.

(8.) Pear SM, Williamson TH, Bettin KM, Gerding DN, Galgiani JN. Decrease in nosocomial Clostridium difficile-associated diarrhea by restricting clindamycin use. Ann Intern Med 1994;120(4):272-277.

(9.) Bartlett JG. Antibiotic-associated colitis. Dis Mon 1984;30(15):1-54.

(10.) Golledge CL, Carson CF, O'Neill GL, Bowman RA, Riley TV Ciprofloxacin and Clostridium difficile-associated diarrhoea. J Antimicrob Chemother 1992;30(2):141-147.

(11.) Yip C, Loeb M, Salama S, Moss L, Olde J. Quinolone use as a risk factor for nosocomial Clostridium difficile-associated diarrhea. Infect ControlHosp Epidemiol 2001;22(9):572-575.

(12.) Bauwens JE, McFarland LV, Melcher SA. Recurrent Clostridium difficile disease following ciprofloxacin use. Ann Pharmacother 1997;31(9):1090.

(13.) McFarland LV, Bauwens JE, Melcher SA, Surawicz CM, Greenberg RN, Elmer GW. Ciprofloxacin-associated Clostridium difficile disease. Lancet 1995;346(8980):977-978.

(14.) Cain DB, O'Connor ME. Pseudomembranous colitis associated with ciprofloxacin. Lancet 1990;336(8720):946.

(15.) Dan M, Samra Z. Clostridium difficile colitis associated with ofloxacin therapy. Am J Med 1989;87(4):479.

(16.) Ozawa TT, Valadez T. Clostridium difficile infection associated with levofloxacin treatment. Tenn Med 2002;95(3):113-115.

(17.) Ortiz-de-Saracho J, Pantoja L, Romero MJ, Lopez R. Moxifloxacininduced Clostridium difficile diarrhea. Ann Pharmacother 2003;37(3):452-453.

(18.) Carroll DN. Moxifloxacin-induced Clostridium difficile-associated diarrhea. Pharmacotherapy 2003;23(11):1517-1519.

(19.) Muto CA, Pokrywka M, Shutt K, Mendelsohn AB, Nouri K, Posey K, Roberts T, Croyle K, Krystofiak S, Patel-Brown S, Pasculle AW, Paterson DL, Saul M, Harrison LH. A large outbreak of Clostridium difficile-associated disease with an unexpected proportion of deaths and colectomies at a teaching hospital following increased fluoroquinolone use. Infect Control Hosp Epidemiol 2005;26(3):273-280.

(20.) McCusker ME, Harris AD, Perencevich E, Roghmann MC. Fluoroquinolone use and Clostridium difficile-associated diarrhea. Emerg Infect Dis 2003;9(6):730-733.

(21.) Dial S, Alrasadi K, Manoukian C, Huang A, Menzies D. Risk of Clostridium difficile diarrhea among hospital inpatients prescribed proton pump inhibitors: cohort and case-control studies. CMAJ 2004;171(1):33-38.

(22.) Cunningham R, Dale B, Undy B, Gaunt N. Proton pump inhibitors as a risk factor for Clostridium difficile diarrhoea. J Hosp Infect 2003;54(3):243-245.

(23.) SAS Institute Inc. SAS/STAT Users Guide, Version 9.1. Cary, NC: SAS Institute Inc., 2002-2003.

(24.) Adams DA, Riggs MM, Donskey CJ. Effect of fluoroquinolone treatment on growth of and toxin production by epidemic and nonepidemic Clostridium difficile strains in the cecal contents of mice. Antimicrob Agents Chemother 2007;51(8):2674-2678.

(25.) Gallagher JC, Du JK, Rose C. Severe pseudomembranous colitis after moxifloxacin use: a case series. Ann Pharmacother 2009;43(1):123-128.

(26.) Dhalla IA, Mamdani MM, Simor AE, Kopp A, Rochon PA, Juurlink DN. Are broad-spectrum fluoroquinolones more likely to cause Clostridium difficile-associated disease? Antimicrob Agents Chemother 2006;50(9):3216-3219.

(27.) Biller P, Shank B, Lind L, Brennan M, Tkatch L, Killgore G, Thompson A, McDonald LC. Moxifloxacin therapy as a risk factor for Clostridium difficile-associated disease during an outbreak: attempts to control a new epidemic strain. Infect Control Hosp Epidemiol 2007;28(2):198-201.

(28.) McFarland LV, Clarridge JE, Beneda HW, Raugi GJ. Fluoroquinolone use and risk factors for Clostridium difficile-associated disease within a Veterans Administration health care system. Clin Infect Dis 2007;45(9):1141-1151.

(29.) Walbrown MA, Aspinall SL, Bayliss NK, Stone RA, Cunningham F, Squier CL, Good CB. Evaluation of Clostridium difficile-associated diarrhea with a drug formulary change in preferred fluoroquinolones. J Manag Care Pharm 2008;14(1):34-40.

(30.) Loo VG, Poirier L, Miller MA, Oughton M, Libman MD, Michaud S, Bourgault AM, Nguyen T, Frenette C, Kelly M, Vibien A, Brassard P, Fenn S, Dewar K, Hudson TJ, Horn R, Rene P, Monczak Y, Dascal A. A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality. N Engl J Med 2005;353(23):2442-2449.

(31.) Kazakova SV, Ware K, Baughman B, Bilukha O, Paradis A, Sears S, Thompson A, Jensen B, Wiggs L, Bessette J, Martin J, Clukey J, Gensheimer K, Killgore G, McDonald LC. A hospital outbreak of diarrhea due to an emerging epidemic strain of Clostridium difficile. Arch Intern Med 2006;166(22):2518-2524.

(32.) Pepin J, Saheb N, Coulombe MA, Alary ME, Corriveau MP, Authier S, Leblanc M, Rivard G, Bettez M, Primeau V, Nguyen M, Jacob CE, Lanthier L. Emergence of fluoroquinolones as the predominant risk factor for Clostridium difficile-associated diarrhea: a cohort study during an epidemic in Quebec. Clin Infect Dis 2005;41(9):1254-1260.

(33.) Deshpande A, Pant C, Jain A, Fraser TG, Rolston DD. Do fluoroquinolones predispose patients to Clostridium difficile associated disease? A review of the evidence. Curr Med Res Opin 2008;24(2):329-333.

(34.) Cunningham R, Dial S. Is over-use of proton pump inhibitors fuelling the current epidemic of Clostridium difficile-associated diarrhoea? J Hosp Infect 2008;70(1):1-6.

(35.) Lowe DO, Mamdani MM, Kopp A, Low DE, Juurlink DN. Proton pump inhibitors and hospitalization for Clostridium difficile-associated disease: a population-based study. Clin Infect Dis 2006;43(10):1272-1276.

(36.) Dial S, Delaney JA, Barkun AN, Suissa S. Use of gastric acid-suppressive agents and the risk of community-acquired Clostridium difficile-associated disease. JAMA 2005;294(23):2989-2995.

(37.) Aseeri M, Schroeder T, Kramer J, Zackula R. Gastric acid suppression by proton pump inhibitors as a risk factor for Clostridium difficile-associated diarrhea in hospitalized patients. Am J Gastroenterol 2008;103(9):2308-2313.

(38.) Dalton BR, Lye-Maccannell T, Henderson EA, Maccannell DR, Louie TJ. Proton pump inhibitors increase significantly the risk of Clostridium difficile infection in a low-endemicity, non-outbreak hospital setting. Aliment Pharmacol Ther 2009;29(6):626-634.

(39.) Pierce PF Jr, Wilson R, Silva J Jr, Garagusi VF, Rifkin GD, Fekety R, Nunez-Montiel O, Dowell VR Jr, Hughes JM. Antibiotic-associated pseudomembranous colitis: an epidemiologic investigation of a cluster of cases. J Infect Dis 1982;145(2):269-274.

(40.) Winston DJ, Lazarus HM, Beveridge RA, Hathorn JW, Gucalp R, Ramphal R, Chow AW, Ho WG, Horn R, Feld R, Louie TJ, Territo MC, Blumer JL, Tack KJ. Randomized, double-blind, multicenter trial comparing clinafloxacin with imipenem as empirical monotherapy for febrile granulocytopenic patients. Clin Infect Dis 2001;32(3):381-390.

(41.) Bodey G, Abi-Said D, Rolston K, Raad I, Whimbey E. Imipenem or cefoperazone-sulbactam combined with vancomycin for therapy of presumed or proven infection in neutropenic cancer patients. Eur J Clin Microbiol Infect Dis 1996;15(8):625-634.

(42.) Freifeld AG, Walsh T, Marshall D, Gress J, Steinberg SM, Hathorn J, Rubin M, Jarosinski P, Gill V, Young RC, et al. Monotherapy for fever and neutropenia in cancer patients: a randomized comparison of ceftazidime versus imipenem. J Clin Oncol 1995;13(1):165-176.

(43.) Baxter R, Ray GT, Fireman BH. Case-control study of antibiotic use and subsequent Clostridium difficile-associated diarrhea in hospitalized patients. Infect Control Hosp Epidemiol 2008;29(1):44-50.

(44.) Tanner J, Khan D, Anthony D, Paton J. Waterlow score to predict patients at risk of developing Clostridium difficile-associated disease. J Hosp Infect 2009;71(3):239-244.

(45.) Garey KW, Dao-Tran TK, Jiang ZD, Price MP, Gentry LO, Dupont HL. A clinical risk index for Clostridium difficile infection in hospitalised patients receiving broad-spectrum antibiotics. J Hosp Infect 2008;70(2):142-147.

Marilee D. Obritsch, PharmD, BCPS, Jeffrey S. Stroup, PharmD, BCPS, Ryan M. Carnahan, PharmD, MS, BCPP, and David N. Scheck, MD

From the Intensive Care Unit (Obritsch) and Department of Infectious Diseases (Scheck), Hillcrest Medical Center, Tulsa, Oklahoma; the Department of Internal Medicine, Oklahoma State University Center for Health Sciences, Tulsa, Oklahoma (Stroup); and the Department of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa (Carnahan).

Supported by a grant from Ortho-McNeil, Inc. Presented at the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy, September 17, 2007. Drs. Stroup and Scheck are consultants for Ortho-McNeil, Inc.; Dr. Scheck is also a consultant for Schering Plough.

Corresponding author: Jeffrey Stroup, PharmD, BCPS, Associate Professor of Medicine, Oklahoma State University Center for Health Sciences, 635 West 11th Street, Tulsa, Oklahoma 74127 (e-mail:
Table 1. Characteristics of subjects with Clostridium
difficile--associated diarrhea and controls

Variable (n = 71)

Female 54%
Age (years [+ or -] SD) 63.5 [+ or -] 15
ICU admission 32%
Recent hospitalization 38%
Admitted from nursing home 13%
Admitted from outside hospital 26%
Charlson Comorbidity Index [+ or -] SD 2.38 [+ or -] 1.9
GI procedure in last 60 days 30%
GI procedure in hospital 39%
Enteral nutrition 26%
Parenteral nutrition 16%
Nasogastric tube 26%
Nasotracheal tube 1%

Variable (n = 142) P value

Female 56% 0.558
Age (years [+ or -] SD) 62.7 [+ or -] 15.6 0.213
ICU admission 32% 0.895
Recent hospitalization 17% 0.0006
Admitted from nursing home 9% 0.322
Admitted from outside hospital 20% 0.341
Charlson Comorbidity Index [+ or -] SD 2.28 [+ or -] 2.02 0.712
GI procedure in last 60 days 4% <0.0001
GI procedure in hospital 16% 0.0006
Enteral nutrition 20% 0.261
Parenteral nutrition 13% 0.407
Nasogastric tube 22% 0.334
Nasotracheal tube 0% 0.991

SD indicates standard deviation; ICU, intensive care unit; GI,

Table 2. Medication exposure of subjects with Clostridium
difficile-associated diarrhea and controls

Medication Variable

Antibiotics Outpatient

Levofloxacin Outpatient
 Duration (days [+ or -] SD)

Moxifloxacin Outpatient
 Duration (days [+ or -] SD)

Imipenem/ Inpatient
cilastatin Duration (days [+ or -] SD)

Proton pump Outpatient
inhibitor Inpatient
 Duration (days [+ or -] SD)

Histamine 2 Outpatient
receptor Inpatient
antagonist Duration (days [+ or -] SD)

Chemotherapy Outpatient
 Duration (days [+ or -] SD)

Steroid Outpatient
 Duration (days [+ or -] SD)

Immunosuppression Outpatient
 Duration (days [+ or -] SD)

Laxative Inpatient

 Cases Controls
Medication (n = 71) (n = 142)

Antibiotics 20% 6%
 93% 82%

Levofloxacin 6% 0%
 10% 12%
 7.8 [+ or -] 2.4 5.7 [+ or -] 4.1

Moxifloxacin 1% <1%
 43% 19%
 6.6 [+ or -] 5.0 6.9 [+ or -] 5.5

Imipenem/ 15% 3%
cilastatin 5.7 [+ or -] 3.4 6.3 [+ or -] 4.2

Proton pump 11% 9%
inhibitor 56% 52%
 11.2 [+ or -] 13.5 7.9 [+ or -] 5.4

Histamine 2 4% 5%
receptor 38% 32%
antagonist 9.2 [+ or -] 7.9 7.1 [+ or -] 6.3

Chemotherapy 0% <1%
 6% 3%
 3 [+ or -] 2 5.8 [+ or -] 3.8

Steroid 9% 4%
 47% 30%
 2.2 [+ or -] 3.8 6.3 [+ or -] 6.7

Immunosuppression 6% 1%
 6% 1%
 7 [+ or -] 4.2 9.5 [+ or -] 4.9

Laxative 50% 15%

Medication P value

Antibiotics 0.004

Levofloxacin 0.0001

Moxifloxacin 0.624

Imipenem/ 0.047

Proton pump 0.627
inhibitor 0.532

Histamine 2 0.823
receptor 0.435

Chemotherapy 0.992

Steroid 0.171

Immunosuppression 0.096

Laxative <0.0001

SD indicates standard deviation.

Table 3. Logistic regression model for variables that increase the
risk of Clostridium difficile--associated diarrhea *

 Odds ratio
 (P value)

GI procedures within 60 days 9.1 (<0.013)
Levofloxacin 8.2 (<0.033) ([dagger])
Moxifloxacin 4.1 (<0.026) ([dagger])
Imipenem/cilastatin 14.9 (<0.014)
Laxative use 20.2 (<0.0001)
Immunosuppressive use 20.7 (<0.034)

 95% confidence

GI procedures within 60 days 1.591-52.022
Levofloxacin 1.176-56.783
Moxifloxacin 1.180-14.067
Imipenem/cilastatin 1.724-129.655
Laxative use 4.291-92.105
Immunosuppressive use 1.258-340.038

* After controlling for recent hospitalizations within 3 months and
Charlson Comorbidity Index.

([dagger]) P > 0.05 (Z test of odds ratio).

Table 4. Outcome, length of stay, and patient disposition of cases
with Clostridium difficile--associated diarrhea and controls

Variable Cases (n = 71)

Clinical outcomes
 Discharge prior to completion of treatment 40%
 Presumed success 37%
Microbiological outcomes
 Eradicated 9%
 Presumed eradication 88%
 Persistence 3%
ICU length of stay (days [+ or -] SD) 7.7 [+ or -] 18.1
Hospital length of stay (days [+ or -] SD) 20.2 [+ or -] 20.8
Discharged to home 51%
Discharged to nursing home 37%
Expired 12%

Variable Controls (n = 142)

Clinical outcomes
 Discharge prior to completion of treatment Not applicable
 Presumed success Not applicable
Microbiological outcomes
 Eradicated Not applicable
 Presumed eradication Not applicable
 Persistence Not applicable
ICU length of stay (days [+ or -] SD) 2.3 [+ or -] 4.7
Hospital length of stay (days [+ or -] SD) 9.6 [+ or -] 6.1
Discharged to home 62%
Discharged to nursing home 25%
Expired 13%

ICU indicates intensive care unit; SD, standard deviation.
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Author:Obritsch, Marilee D.; Stroup, Jeffrey S.; Carnahan, Ryan M.; Scheck, David N.
Publication:Baylor University Medical Center Proceedings
Article Type:Clinical report
Geographic Code:1U7OK
Date:Oct 1, 2010
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