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1.
Int J Clin Pharm ; 34(2): 282-5, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22331444

ABSTRACT

BACKGROUND: After medical center implementation of 2009 ASHP/IDSA guidelines, we evaluated the appropriateness of vancomycin dosing and TDM. OBJECTIVE: Our primary objectives were to assess short term effects on (1) appropriateness of initial vancomycin dosing, (2) appropriateness of sampling of plasma levels, before and after implementation of guidelines. METHOD: The study was conducted in two phases, pre-guideline and post-guideline implementation. The interventions included (1) Nurses and phlebotomist education regarding the appropriate timing of vancomycin sampling, (2) A nomogram for appropriate initial dosing that was distributed to medical staff. Patient demographics, dosing and timing of sampling were collected in eligible patients and assessed for appropriateness. RESULTS: The appropriateness of the prescribed dose increased from 51% (128/253) of patients during the pre period to 78% (155/200) (p < 0.0001) during the post period. Similarly, overall appropriateness of sampling of vancomycin troughs at steady state improved from 36% (63/173) pre to 55% (106/191) (p < 0.03) post. Specifically, the appropriate timing of troughs (within 30 min of the next dose) increased from 37% (64/173) during the pre period to 78% (149/191) during the post period (p < 0.0001). Conclusion Adoption of the guidelines with associated training resulted in significant short term improvement in vancomycin dosing and TDM.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Drug Monitoring/standards , Pharmacy Service, Hospital/standards , Practice Patterns, Physicians'/standards , Vancomycin/administration & dosage , Academic Medical Centers/standards , Anti-Bacterial Agents/blood , Anti-Bacterial Agents/pharmacokinetics , Drug Utilization , Education, Medical, Continuing , Education, Nursing, Continuing , Education, Pharmacy, Continuing , Guideline Adherence , Health Personnel/education , Humans , Nomograms , Practice Guidelines as Topic , Prospective Studies , San Francisco , Time Factors , Vancomycin/blood , Vancomycin/pharmacokinetics
2.
J Hosp Med ; 1(1): 7-12, 2006 Jan.
Article in English | MEDLINE | ID: mdl-17219465

ABSTRACT

BACKGROUND: Limited data exist on the effectiveness of ceftriaxone plus doxycycline in the treatment of patients hospitalized with community-acquired pneumonia (CAP). METHODS: We performed a retrospective cohort study of all adults hospitalized for pneumonia between January 1999 and July 2001 at an academic medical center. Outcomes were compared for patients with CAP treated with ceftriaxone plus doxycycline versus other appropriate initial empiric antibiotic therapies. Outcomes were adjusted with the use of a propensity score to account for differences in patient characteristics and illness severity between groups. RESULTS: A total of 216 patients were treated with ceftriaxone plus doxycycline and 125 received other appropriate initial empiric antibiotic therapies. After adjustment, use of ceftriaxone plus doxycycline was associated with reduced inpatient mortality (OR = 0.26, 95% CI: 0.08-0.81) and 30-day mortality (OR = 0.37, 95% CI: 0.17-0.81), but not with length of stay or readmission rates. Analysis of a subset of the sample that excluded patients admitted from nursing homes, patients admitted to the ICU, and patients diagnosed with aspiration also showed reduced inpatient mortality with the use of ceftriaxone plus doxycycline. CONCLUSIONS: The use of ceftriaxone plus doxycycline as an initial empiric therapy for patients hospitalized with CAP appears safe and effective, and its potential superiority should be evaluated prospectively.


Subject(s)
Ceftriaxone/administration & dosage , Community-Acquired Infections/drug therapy , Doxycycline/administration & dosage , Hospitalization , Pneumonia/drug therapy , Adult , California , Community-Acquired Infections/epidemiology , Drug Therapy, Combination , Humans , Length of Stay , Pneumonia/epidemiology , Retrospective Studies , Treatment Outcome
3.
Jt Comm J Qual Patient Saf ; 31(8): 469-75, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16156195

ABSTRACT

BACKGROUND: In response to vancomycin-resistant bacteria, particularly vancomycin-resistant enterococci (VRE), measures have been recommended to improve on the appropriate use of vancomycin. METHODS: Intervention 1 consisted of an automatic 72-hour vancomycin stop order; Intervention 2, a standardized procedure for sampling of blood cultures; and Intervention 3, an interdisciplinary critical care team. RESULTS: After Intervention 1, inappropriate use decreased, particularly in treatment of febrile neutropenia and undocumented gram-positive infections. After Intervention 2, the baseline rate of inappropriately drawn blood cultures (IDBCs) was unchanged, and use in patients with IDBCs was comparable during both periods. Before Intervention 3, 38/55 orders continuing > 72 hours were considered inappropriate versus 24/53 (p < .025) after. After the interventions, hospitalwide vancomycin use was reduced. Yet the overall rate of VRE infection initially decreased but then increased once again over time. DISCUSSION: Despite substantial reduction in hospitalwide vancomycin use, the impact on the overall rate of VRE was inconsistent and ward dependent.


Subject(s)
Enterococcus/drug effects , Quality Assurance, Health Care/methods , Vancomycin Resistance , Vancomycin/therapeutic use , California , Drug Prescriptions/standards , Humans
4.
Dis Mon ; 48(4): 239-48, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12021756

ABSTRACT

We studied whether pharmacists involved in discharge planning can improve patient satisfaction and outcomes by providing telephone follow-up after hospital discharge. We conducted a randomized trial at the General Medical Service of an academic teaching hospital. We enrolled General Medical Service patients who received pharmacy-facilitated discharge from the hospital to home. The intervention consisted of a follow-up phone call by a pharmacist 2 days after discharge. During the phone call, pharmacists asked patients about their medications, including whether they obtained and understood how to take them. Two weeks after discharge, we mailed all patients a questionnaire to assess satisfaction with hospitalization and reviewed hospital records. Of the 1,958 patients discharged from the General Medical Service from August 1, 1998 to March 31, 1999, 221 patients consented to participate. We randomized 110 to the intervention group (phone call) and 111 to the control group (no phone call). Patients returned 145 (66%) surveys. More patients in the phone call than the no phone call group were satisfied with discharge medication instructions (86% vs. 61%, P = 0.007). The phone call allowed pharmacists to identify and resolve medication-related problems for 15 patients (19%). Twelve patients (15%) contacted by telephone reported new medical problems requiring referral to their inpatient team. Fewer patients from the phone call group returned to the emergency department within 30 days (10% phone call vs. 24% no phone call, P = 0.005). A follow-up phone call by a pharmacist involved in the hospital care of patients was associated with increased patient satisfaction, resolution of medication-related problems, and fewer return visits to the emergency department.


Subject(s)
Patient Discharge , Patient Satisfaction , Pharmacy Service, Hospital , Telephone , Female , Humans , Male , Middle Aged , San Francisco , Surveys and Questionnaires
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