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Reducing risk of Clostridium difficile infection and overall use of antibiotic in the outpatient treatment of urinary tract infection.
Ge, Ivy Y; Fevrier, Helene B; Conell, Carol; Kheraj, Malika N; Flint, Alexander C; Smith, Darvin S; Herrinton, Lisa J.
Affiliation
  • Ge IY; Inpatient Pharmacy, Kaiser Permanente Northern California South San Francisco Medical Center, 1200 El Camino Real, 3rd Floor, South San Francisco, CA 94080, USA.
  • Fevrier HB; Division of Research, Kaiser Permanente, Oakland, CA, USA.
  • Conell C; Division of Research, Kaiser Permanente, Oakland, CA, USA.
  • Kheraj MN; Department of Infectious Disease, Kaiser Permanente Redwood City Medical Center, Redwood City, CA, USA.
  • Flint AC; Department of Neurology, Kaiser Permanente Redwood City Medical Center, Redwood City, CA, USA.
  • Smith DS; Department of Infectious Disease, Kaiser Permanente Redwood City Medical Center, Redwood City, CA, USA.
  • Herrinton LJ; Division of Research, Kaiser Permanente, Oakland, CA, USA.
Ther Adv Urol ; 10(10): 283-293, 2018 Oct.
Article in En | MEDLINE | ID: mdl-30186366
ABSTRACT

BACKGROUND:

Risk of community-acquired Clostridium difficile infection (CA-CDI) following antibiotic treatment specifically for urinary tract infection (UTI) has not been evaluated.

METHODS:

We conducted a nested case-control study at Kaiser Permanente Northern California, 2007-2010, to assess antibiotic prescribing and other factors in relation to risk of CA-CDI in outpatients with uncomplicated UTI. Cases were diagnosed with CA-CDI within 90 days of antibiotic use. We used matched controls and confirmed case-control eligibility through chart review. Antibiotics were classified as ciprofloxacin (most common), or low risk (nitrofurantoin, sulfamethoxazole/trimethoprim), moderate risk, or high risk (e.g. cefpodoxime, ceftriaxone, clindamycin) for CDI. We computed the adjusted odds ratios (ORs) and 95% confidence intervals (CIs) for the relationship of antibiotic treatment for uncomplicated UTI and history of relevant gastrointestinal comorbidity (including gastrointestinal diagnoses, procedures, and gastric acid suppression treatment) with risk of CA-CDI using logistic regression analysis.

RESULTS:

Despite the large population, only 68 cases were confirmed with CA-CDI for comparison with 112 controls. Female sex [81% of controls, adjusted odds ratio (OR) 6.3, CI 1.7-24), past gastrointestinal comorbidity (prevalence 39%, OR 2.3, CI 1.1-4.8), and nongastrointestinal comorbidity (prevalence 6%, OR 2.8, CI 1.4-5.6) were associated with increased CA-CDI risk. Compared with low-risk antibiotic, the adjusted ORs for antibiotic groups were as follows ciprofloxacin, 2.7 (CI 1.0-7.2); moderate-risk antibiotics, 3.6 (CI 1.2-11); and high-risk antibiotics, 11.2 (CI 2.4-52).

CONCLUSIONS:

Lower-risk antibiotics should be used for UTI whenever possible, particularly in patients with a gastrointestinal comorbidity. However, UTI can be managed through alternative approaches. Research into the primary prevention of UTI is urgently needed.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Language: En Journal: Ther Adv Urol Year: 2018 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Language: En Journal: Ther Adv Urol Year: 2018 Document type: Article Affiliation country: United States
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