Emerg Infect DisEmerging Infect. DisEIDEmerging Infectious Diseases1080-60401080-6059Centers for Disease Control and Prevention16318696336674605-033610.3201/eid1110.050336ResearchResearchVancomycin and Home Health CareVancomycin and Home Health CareFraserThomas G.*1StosorValentina*WangQiongAllenAnneZembowerTeresa R.*Northwestern University Feinberg School of Medicine, Chicago, Illinois, USAUniversity of Illinois at Chicago School of Public Health, Chicago, Illinois, USANorthwestern Memorial Hospital, Chicago, Illinois, USAAddress for correspondence: Teresa R. Zembower, Department of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, 676 North Saint Clair St, Suite 200, Chicago, IL 60611, USA; fax: 312-695-5088; email: t-zembower@northwestern.edu102005111015581564

Microbiologic diagnosis before hospital discharge and physician education may limit inappropriate vancomycin use in homecare patients.

The Hospital Infection Control Practices Advisory Committee published guidelines for prudent use of vancomycin to combat increasing resistance to antimicrobial drugs. Studies examining compliance with these guidelines primarily involve hospitalized patients. The growing practice of home use of antimicrobial drugs led to this retrospective cohort study that evaluated parenteral vancomycin use in patients receiving it through a homecare agency. We found that 39.2% of outpatients received vancomycin outside the guidelines, mainly because of prolonged empiric therapy, dosing convenience, and prolonged use after surgery. Patients were more likely to receive vancomycin appropriately if they were >65 years of age, had a history of malignancy, or were discharged from a medical service. In addition, obtaining wound cultures and attempting a microbiologic diagnosis led to more appropriate vancomycin use. Recommendations for prudent vancomycin use are often overlooked when selecting antimicrobial drugs for home infusion. The public health impact of this practice remains unknown.

Keywords: vancomycinhome healthcareHICPAC guidelinesoutpatient parenteral antimicrobial therapyantimicrobial resistanceresearch

Vancomycin is an important agent for the treatment of serious infections caused by gram-positive bacteria (1). Over the past 3 decades, its use has steadily increased because of increasing prevalence of β-lactam-resistant nosocomial pathogens, particularly, methicillin-resistant Staphylococcus aureus (MRSA) and coagulase-negative staphylococci (CoNS) (2,3). A consequence of this increased use has been the emergence and spread of vancomycin-resistant enterococci, the isolation of S. aureus with reduced susceptibility to glycopeptides, and, most recently, reports of infections caused by vancomycin-resistant S. aureus (46).

Antimicrobial stewardship guidelines have been developed to ensure that vancomycin is used appropriately and retains its viability in the therapeutic armamentarium. The most broadly accepted benchmark was published by the Hospital Infection Control Practices Advisory Committee (HICPAC) of the Centers for Disease Control and Prevention (7). These guidelines and most efforts to control use of antimicrobial drugs target the hospital setting (812). However, the prevalence of drug-resistant pathogens in outpatient and ambulatory settings is increasing, as demonstrated by the prevalence of penicillin-resistant pneumococci and recent emergence of community-onset MRSA (13,14). With an increasing number of patients receiving home infusions of antimicrobial drugs, the appropriateness of choices of drugs for outpatients warrants scrutiny. Guidelines for the administration of outpatient parenteral antibiotic therapy (OPAT) noted this and encouraged adherence to HICPAC guidelines (15).

We conducted a retrospective cohort study of patients discharged from an academic medical center to complete a course of intravenous vancomycin at home. The main objectives were to describe the epidemiology of outpatients receiving vancomycin through a home healthcare agency, determine the appropriateness of outpatient vancomycin prescriptions according to HICPAC guidelines, and examine factors associated with outpatient vancomycin use that conformed to HICPAC guidelines.

MethodsStudy Setting and Patient Population

Northwestern Memorial Hospital (NMH) is a 725-bed teaching hospital in Chicago, Illinois. Northwestern Memorial Home Health Care, Inc. (NMHHC), the home healthcare agency affiliated with NMH, receives >200 annual referrals for home infusion of antimicrobial agents.

This study included all inpatients at NMH referred to NMHHC to complete a course of intravenous vancomycin therapy from December 1997 to April 2002. Patients were excluded if they were <16 years of age, admitted to the hospital already receiving vancomycin, discharged to any other facility, or received care from another homecare agency before referral to NMHHC. For patients with multiple referrals to NMHHC for vancomycin therapy, only their first treatment episode was included. During this study, although vancomycin use guidelines were published and distributed within NMH, no formal enforcement policy existed within the hospital or homecare setting. The institutional review board of Northwestern University reviewed and approved the study protocol.

Clinical Data

All data were originally collected as part of routine patient care. For this study, clinical data were abstracted retrospectively by review of existing inpatient medical records, home health referral forms, and the inpatient pharmacy database. The data abstractor had no part in the original data collection. The following data were abstracted: demographic information, length of hospital stay, admitting service, insurance status, allergy to β-lactam antimicrobial drugs, level of serum creatinine on the day of discharge, history of end-stage renal disease requiring dialysis, infectious diseases consultation, use of vancomycin in the hospital, reason(s) for vancomycin use, and discharge diagnoses per ICD-9 codes. ICD-9 codes were used to calculate a mean Charlson comorbidity score for each patient (16,17). With 1 exception, the presence of infectious syndromes was determined by review of ICD-9 diagnoses. A diagnosis of bloodstream infection was assigned if multiple positive blood cultures were documented, regardless of coded diagnoses. Because of the retrospective nature of the evaluation, all recorded allergies to β-lactam antimicrobial drugs were considered potentially serious.

Microbiologic Data

The microbiology records spanning the length of the hospitalization for each patient were reviewed. A microbiologic evaluation occurred if cultures were obtained that reasonably corresponded to the infectious diagnosis requiring the use of vancomycin. Record review focused on collection of cultures from blood, other sterile sites, urine, sputum, intravenous catheters or other foreign bodies, and wounds or tissues. Bacterial isolates that were specifically recorded were gram-positive organisms whose treatment might prompt or warrant the use of vancomycin, including methicillin-susceptible S. aureus, MRSA, CoNS, streptococci, ampicillin-resistant or -susceptible enterococci, and Corynebacterium jeikeium.

Evaluation of Vancomycin Use

HICPAC guidelines served as the basis for determining whether patients received parenteral vancomycin per guidelines or outside guidelines (Table 1). The guidelines pertaining to prophylaxis for endocarditis (1C), surgical procedures (1D and 2A), and low-birthweight infants (2G) did not apply and were disregarded.

HICPAC guidelines for prudent use of parenteral vancomycin*
1) Situations in which use of vancomycin is appropriate
A) Treatment of serious infections caused by β-lactam-resistant, gram-positive organisms
B) Treatment of infections caused by gram-positive microorganisms in patients with serious allergies to β-lactam antimicrobial agents
C) Prophylaxis, as recommended by the American Heart Association, after certain procedures in patients at high risk for endocarditis
D) Prophylaxis for major surgical procedures involving implantation of prosthetic materials or devices at institutions that have a high rate of infections caused by MRSA or methicillin-resistant Staphylococcus epidermidis
2) Situations in which use of vancomycin should be discouraged
A) Routine surgical prophylaxis, unless patient has life-threatening allergy to β-lactam antimicrobial drugs
B) Empiric antimicrobial therapy for febrile neutropenic patient, unless evidence indicates patient has infection caused by gram-positive microorganisms and prevalence of MRSA infections in hospital is substantial
C) Treatment in response to single blood culture positive for coagulase-negative staphylococci, if other blood cultures taken during same timeframe are negative
D) Continued empiric use for presumed infections in patients whose cultures are negative for β-lactam-resistant gram-positive microorganisms
E) Systemic or local (e.g., antimicrobial drug lock therapy)† prophylaxis for infection or colonization of intravascular catheters
F) Eradication of MRSA colonization
G) Routine prophylaxis for very-low-birthweight infants
H) Routine prophylaxis for dialysis patients
I) Treatment (chosen for dosing convenience) of infections caused by β-lactam-sensitive, gram-positive microorganisms in patients with renal failure

*Summarized from reference 7. HICPAC, Hospital Infection Control Practices Advisory Committee; MRSA, methicillin-resistant Staphylococcus aureus.
†Instilling a high concentration of antimicrobial drug to which organism is susceptible into lumen of catheter in attempt to sterilize it.

In addition, vancomycin use was determined to fall outside HICPAC guidelines for the following situations: 1) treatment of CoNS from superficial wound swabs, or respiratory or urine specimens unless they occurred in the setting of bacteremia; 2) dosing convenience defined as initial treatment with a β-lactam antimicrobial drug during hospitalization with a therapeutic change to vancomycin within 24 h of discharge that was not dictated by culture results or allergy; 3) prolonged administration of an antimicrobial agent after implantation of prosthetic materials; 4) treatment of cellulitis without identification of a β-lactam-resistant pathogen (additionally, the empiric switch to vancomycin because of slow resolution of cellulitis was considered noncompliant use); and 5) ongoing treatment of infection in a patient with a history of MRSA colonization in the absence of a diagnostic culture. If the use of vancomycin met >1 of these specified criteria, each was included in data collection.

Statistical Analysis

Data were collected on a standardized form and entered onto spreadsheets (Excel 2000, Microsoft Corporation, Redmond, WA, USA). To evaluate predictors for compliance with vancomycin use guidelines, discrete variables were described by percentages and compared by using chi-square or Fisher exact tests as appropriate. Continuous variables were described by means and evaluated by using Student t test. Variables with a p value <0.05 by univariate analysis were evaluated by stepwise logistic regression for inclusion in the final model. SAS version 8.2 for personal computers (SAS Institute Inc., Cary, NC, USA) was used for statistical analysis.

Results

During the study period, NMHHC received 323 patient referrals for continuation of parenteral vancomycin therapy after hospitalization. The records of 27 patients (8.4%) could not be located and were not included in the study. Thus, the final analysis included 296 patients. Table 2 summarizes the criteria that determined whether vancomycin was prescribed within HICPAC guidelines. One hundred eighty patients (60.8%), 5 of whom met >1 criteria for appropriate use, received vancomycin within guidelines. A total of 118 (65.6%) were treated for infections caused by β-lactam-resistant, gram-positive bacteria. Sixty-seven patients (37.2%) received vancomycin for a reported allergic reaction to β-lactam antimicrobial drugs. Although only the first referral for home vancomycin was analyzed for each patient, 44 (14.9%) were referred multiple times to receive vancomycin as outpatients (2–8 referrals per patient) during this study.

Comparison of HICPAC guidelines with home infusion use of vancomycin in 296 patients*
No. (%)
Manner in which vancomycin use met guidelines180 (60.8)
Treatment of infections with β-lactam-resistant, gram-positive bacteria118 (65.6)
Treatment of gram-positive infections in patients with allergies to β-lactam agents67 (37.2)
Manner in which vancomycin use did not meet guidelines116 (39.2)
Continued empiric vancomycin use in patients with negative or no cultures84 (72.4)
Use of vancomycin for dosing convenience18 (15.5)
Prolonged administration of antimicrobial drugs after implantation of prosthetic materials or devices13 (11.2)
Treatment of a single blood culture showing coagulase-negative staphylococci9 (7.8)

*Some patients fulfilled >1 criteria. HICPAC, Hospital Infection Control Practices Advisory Committee.

Of the 296 patients, 116 (39.2%), 8 of whom met >1 criteria, received vancomycin outside HICPAC guidelines. Eighty-four (72.4%) cases were for continued empiric treatment of presumed infections in patients whose cultures were negative or not obtained. This practice was prevalent across all services. Dosing convenience led to the use of the drug in 18 (15.5%) patients, 12 (67%) of whom were admitted to a medical service. In 13 patients (11.2%), home-infusion vancomycin was continued after major surgical procedures involving implanted devices. This practice occurred exclusively in orthopedic and neurosurgery services. Finally, in 9 patients (7.8%), vancomycin was used to treat infection with a CoNS isolate from a single blood culture.

Demographic and clinical characteristics are shown in Table 3. Patients whose use of vancomycin followed guidelines were older than those whose use did not follow guidelines (mean age 53.6 years vs. 48.9 years, p = 0.016). No significant differences were noted in sex or ethnicity, although African-Americans showed a trend toward receiving vancomycin within guidelines (p = 0.054). Appropriate vancomycin use was more likely after a longer mean hospital stay (12.2 days vs. 9.5 days, p = 0.007). No significant differences were noted in the mean Charlson comorbidity score or frequency of diagnosed coexisting medical conditions between the 2 groups with the exception of a history of malignancy (21.7% vs. 10.3%, p = 0.012) among patients who received vancomycin according to guidelines. Insurance status did not differ between groups.

Demographic and clinical characteristics of 296 patients referred for home infusions of vancomycin from December 1997 through May 2002*
CharacteristicUse per guidelines, N = 180Use outside guidelines, N = 116p value†
Mean age, years (range)53.6 (19–90)48.9 (19–86)0.016
Male, no. (%)109 (60.6)76 (65.5)0.389
Ethnicity, no. (%)
Caucasian100 (55.6)75 (64.7)0.120
African-American52 (28.9)22 (19.0)0.054
Asian3 (1.7)00.283
Hispanic7 (3.9)2 (1.7)0.490
Other18 (10.0)15 (12.9)0.434
Mean length of stay, days (range)12.2 (2–52)9.5 (2–67)0.007
Coexisting conditions, no. (%)
Diabetes mellitus47 (26.1)28 (24.1)0.703
Malignancy39 (21.7)12 (10.3)0.012
Spinal cord injury28 (15.6)13 (11.2)0.290
Decubitus ulcer31 (17.2)11 (9.5)0.063
Acute renal failure15 (8.3)6 (5.2)0.301
ESRD5 (2.8)1 (0.9)0.409
Immunocompromised status10 (5.6)8 (6.9)0.637
HIV3 (1.7)1 (0.9)1.000
Charlson score, mean (range)1.4 (0–8)1.1 (0–14)0.217
Insurance status, no. (%)176 (97.8)116 (100)0.158
Private121 (67.2)86 (74.1)0.205
Medicare74 (41.1)36 (31.0)0.080
Medicaid48 (26.7)25 (21.6)0.319
Discharging service, no. (%)
Medical108 (60.0)44 (37.9)<0.001
General medicine66 (36.7)29 (25.0)0.036
Medicine subspecialties29 (16.1)10 (8.6)0.063
Hematology/oncology13 (7.2)5 (4.3)0.306
Surgical67 (37.2)69 (59.5)<0.001
General surgery2 (1.1)4 (3.5)0.215
Transplant surgery5 (2.8)6 (5.2)0.350
Vascular surgery14 (7.8)7 (6.0)0.569
Orthopedics/neurosurgery31 (17.2)41 (35.3)<0.001
Other surgical subspecialties15 (8.3)11 (9.5)0.733
Other hospital services5 (2.8)3 (2.6)1.000
Consultation by infectious diseases, no. (%)85 (47.2)58 (50.0)0.641

*ESRD, end-stage renal disease requiring dialysis; immunocompromised status, immunocompromised from causes other than HIV.
†Values <0.05 were considered significant.

Compliance with HICPAC guidelines varied according to the inpatient prescribing service. Appropriate prescriptions for vancomycin were more likely to be preceded by discharge from a medical service (60.0% vs. 37.9%, p<0.001). This finding was true both for discharges from general medicine and medical subspecialty services, with the exception of hematology/oncology. More episodes of vancomycin infusion outside guidelines followed discharge from a surgical service (59.5% vs. 37.2%, p<0.001), namely, orthopedic and neurosurgery services (35.3% vs. 17.2%, p<0.001). Inpatient consultation by an infectious diseases specialist did not affect the appropriateness of home vancomycin prescriptions by managing services (p = 0.641).

The infection diagnoses of patients referred for home infusions of vancomycin are outlined in Table 4. Patients were more likely to receive vancomycin per guidelines in the setting of bloodstream (33.9% vs. 13.8%, p<0.001) and urinary tract infections (20% vs. 11.2%, p = 0.042). The microbiologic investigations undertaken and the organisms identified during hospitalization are delineated in Table 5. Appropriate use of vancomycin was more likely to follow an attempt to make a microbiologic diagnosis (96.1% vs. 77.6%, p<0.001). More blood, urine, and wound cultures were obtained in this group, and the number of cultures obtained was higher when vancomycin was used appropriately.

Infection diagnoses in patients referred for home infusions of vancomycin
Diagnosis*Use per guidelines, no. (%), N = 180Use outside guidelines, no. (%), N = 116p value†
Skin or soft tissue infection89 (49.4)51 (44.0)0.356
Osteomyelitis or septic arthritis30 (16.7)25 (21.6)0.294
Postoperative wound infection38 (21.1)19 (16.4)0.310
Orthopedic device-related infection5 (2.8)7 (6.0)0.227
Central nervous system infection‡3 (1.7)6 (5.2)0.161
Urinary tract infection36 (20.0)13 (11.2)0.042
Pneumonia9 (5.0)1 (0.9)0.095
Bloodstream infection61 (33.9)16 (13.8)<0.001
Vascular device infection21 (11.7)10 (8.6)0.398
Infective endocarditis8 (4.4)5 (4.3)0.956

*Some patients had >1 diagnosis.
†Values <0.05 were considered significant.
‡Includes shunt infections.

Microbiologic investigations and results for home infusions of vancomycin*
Investigation or resultUse per guidelines, no. (%), N = 180Use outside guidelines, no. (%), N = 116p value†
Microbiologic diagnostic attempt173 (96.1)90 (77.6)<0.001
Cultures by site
Blood137 (76.1)74 (63.8)0.022
Sterile site25 (13.9)11 (9.5)0.258
Urine96 (53.3)48 (41.4)0.045
Sputum17 (9.4)6 (5.2)0.180
Wound96 (53.3)45 (38.8)0.015
Other culture15 (8.3)11 (9.5)0.733
>1 culture136 (75.6)65 (56.0)<0.001
Bacterial isolates
MRSA81 (45.0)2 (1.7)‡§
Coagulase-negative staphylococci59 (32.8)20 (17.2)
Ampicillin-resistant enterococci3 (1.7)0
Methicillin-susceptible S. aureus16 (8.9)19 (16.4)
Other streptococci and enterococci52 (28.9)18 (15.5)
Corynebacterium jeikeium2 (1.1)0
Culture considered contaminated20 (11.1)20 (17.2)

*MRSA, methicillin-resistant Staphylococcus aureus.
†Values <0.05 were considered significant.
‡The 2 patients outside the guidelines with an MRSA culture included 1 patient with MRSA in the urine but no diagnosis of a urinary tract infection, and 1 with a positive intravascular catheter tip culture but no evidence of infection.
§A p value is not included because infection with these isolates was 1 factor used to determine whether vancomycin was given per guidelines.

Results of the multivariate analysis are shown in Table 6. Patients <65 years of age were less likely to receive appropriate vancomycin (odds ratio [OR] 0.50, 95% confidence interval [CI] 0.26–0.94). Appropriate use of vancomycin was more likely to occur after discharge from a medical service rather than a surgical service (OR 2.62, 95% CI 1.53–4.48). Although discharge from a hematology/oncology service was not associated with appropriate use of vancomycin, patients with a history of malignancy were more likely to receive vancomycin within HICPAC guidelines (OR 3.02, 95% CI 1.40–6.53). Obtaining a wound culture was associated with appropriate use of vancomycin (OR 2.08, 95% CI 1.19–3.64). Finally, patients who underwent any microbiologic evaluation were more likely to receive appropriate vancomycin through home care (OR 5.93, 95% CI 2.26–15.54).

Factors associated with appropriate use of vancomycin by multivariate analysis using stepwise logistic regression analysis
VariableOdds ratio (95% CI)*p value
Attempt at a microbiologic diagnosis5.93 (2.26–15.54)0.0003
Discharge from a medical service2.62 (1.53–4.48)0.0004
History of a malignancy3.02 (1.40–6.53)0.0050
Obtaining a wound culture2.08 (1.19–3.64)0.0107
Age <650.50 (0.26–.094)0.0321

*CI, confidence interval.

Discussion

This study examined a large group of patients referred for home infusions of vancomycin over a 5-year period and applied established guidelines to determine if outpatient use conformed to a widely accepted benchmark. A total of 39.2% of the prescriptions were given outside guidelines. Several authors have applied these HICPAC guidelines to evaluate inpatient use of vancomycin and found the incidence of outside guidelines use to range from 36% to 79% (11,12,18,19). Our study, however, is the first to critically evaluate the appropriateness of vancomycin in the outpatient setting.

The most common reason for outside guidelines use of vancomycin was continuation of empiric therapy in patients without a culture-defining indication. Singer et al. have found similar results in hospitalized patients (12). In contrast, other studies found that the most common reasons for inappropriate inpatient prescriptions for vancomycin were surgical prophylaxis and failure to modify prescriptions for antimicrobial drugs based on culture results (19,20).

We found that the other reasons for vancomycin use outside guidelines were dosing convenience, prolonged use after surgical procedures, and treatment of CoNS isolated from a single blood culture. Use for dosing convenience is likely underestimated (15.5%) because of the conservative definition used in this retrospective analysis. The incidence of vancomycin use for prolonged periods after implantation of devices and for the treatment of CoNS from a single blood culture was less than the incidence among inpatients (12,19). This incidence may reflect that continuing vancomycin for these indications is more convenient in the inpatient setting and that physicians are likely to reevaluate the true need for outpatient vancomycin in these circumstances.

Examined data showing the prescribing patterns of physicians demonstrate that patients discharged from a medical service are more likely to receive vancomycin appropriately. Of surgical subspecialists, orthopedic and neurosurgeons were more likely to prescribe vancomycin outside guidelines. These prescribing differences are consistent with the findings of inpatient vancomycin use evaluations (2124). Although patients with a history of malignancy received vancomycin according to HICPAC guidelines, hematology/oncology was the only medical service not associated with appropriate use. These results suggest that the vancomycin-prescribing practices of certain subspecialists offer the opportunity for education regarding the existence of and rationale for such guidelines and targeted intervention to reduce unnecessary outpatient vancomycin usage (25). Only 6 patients with end-stage renal disease received vancomycin through homecare. Intuitively, one might expect more vancomycin use in this patient population; however, this finding probably reflects that these patients receive vancomycin during hemodialysis and, thus, do not require referral to home health. In contrast to other studies, consultation by infectious diseases physicians did not impact compliance (2628). This finding warrants further examination to determine if infectious diseases physicians recommend vancomycin for use outside of HICPAC guidelines or if their recommendations are disregarded.

If a microbiologic evaluation was attempted, vancomycin use was more likely to follow guidelines. Obtaining wound cultures was also associated with appropriate use. A thorough microbiologic evaluation aids in clinical decision making. When clinicians have culture and susceptibility results, they are more likely to use vancomycin appropriately, particularly for patients with skin and soft tissue infections.

Patients >65 years of age were more likely to receive vancomycin per guidelines. The reasons for this are unclear but were not impacted by insurance status. This finding probably reflects that patients referred for intravenous antimicrobial drugs through homecare either have insurance that will reimburse for the service or have the ability to pay for the drugs.

This study had several limitations because of its retrospective nature. A substantial number of patients were classified in the compliant group on the basis of a reported allergy to β-lactam drugs. Because we were unable to determine the nature of reported allergies to penicillin, all allergies were assumed to be serious in nature. Thus, this study overestimates appropriate vancomycin use for this purpose. Another limitation of this analysis is the inability to account for the impact of vancomycin courses patients may have received before this study. Finally, this study does not address the financial consideration that influenced the choice of antimicrobial drug. Other investigators have explored this issue and found that the costs of outpatient vancomycin therapy are substantial (29). The patients in this study were preselected to the extent that they were able to receive vancomycin at home.

HICPAC guidelines were developed to promote judicious use of vancomycin in an attempt to curtail the spread of vancomycin-resistant enterococci and forestall the development of S. aureus with reduced susceptibility to glycopeptides. Although these guidelines were initially applied to the inpatient setting, the OPAT guidelines have recommended that they also apply to outpatients receiving vancomycin. Apart from vancomycin, however, the OPAT guidelines lack information regarding choices of antimicrobial drugs for outpatients. In addition, they do not clearly prioritize conscientious use of antimicrobial drugs above other considerations, such as cost and dosing convenience, when choosing outpatient therapy. These issues need to be addressed as the emergence and spread of antimicrobial-resistant gram-positive pathogens in the community continue to increase.

One in 1,000 patients in the United States is estimated to receive outpatient infusion of antimicrobial drugs each year (15). The trend toward increased inpatient acuity and shorter hospital stay will undoubtedly increase this practice. Our study on first-time referrals from 1 tertiary care hospital to its homecare agency represents only a subset of vancomycin use in the community. The propensity for readmissions and repeated referrals of these chronically ill patients must be considered when analyzing the impact of outpatient vancomycin use. In addition, vancomycin administered by other homecare agencies, extended care facilities, outpatient infusion centers, and outpatient dialysis centers all contribute to its burgeoning use outside the hospital. Our study indicates that further investigations into the consequences of this practice on individual persons and the community are warranted. Do the favorable pharmacokinetics and economic attributes of vancomycin that make it attractive for home infusion outweigh the potential consequences of unnecessarily broad-spectrum gram-positive coverage? Further studies are needed to address these issues if we are to understand the dynamics of resistant pathogens in the community and the overall emergence and spread of antimicrobial resistance.

Suggested citation for this article: Fraser TG, Stosor V, Wang Q, Allen A, Zembower TR. Vancomycin and home health care. Emerg Infect Dis [serial on the Internet]. 2005 Oct [date cited]. http://dx.doi.org/10.3201/eid1110.050336

Current affiliation: Cleveland Clinic Foundation, Cleveland, Ohio, USA

This work was supported by Northwestern University Feinberg School of Medicine.

Dr Fraser is an associate hospital epidemiologist in the Division of Medicine, Department of Infectious Diseases, Cleveland Clinic Foundation. His research interests include hospital-acquired infections, antimicrobial stewardship, and management of cardiovascular infections, including infective endocarditis.

ReferencesWilhelm MP, Estes L Symposium on antimicrobial agents—Part XII. Vancomycin. Mayo Clin Proc. 1999;74:92835 10.4065/74.9.92810488798Ena J, Dick RW, Jones RN, Wenzel RP The epidemiology of intravenous vancomycin usage in a university hospital. JAMA. 1993;269:598602 10.1001/jama.1993.035000500760298240468Fridkin SK, Edwards JR, Pichette SC, Pryor ER, McGowan JE Jr, Tenover FC, Determinants of vancomycin use in adult intensive care units in 41 United States hospitals. Clin Infect Dis. 1999;28:111925 10.1086/51475210452645Centers for Disease Control and Prevention Nosocomial enterococci resistant to vancomycin—United States, 1989–1993. MMWR Morb Mortal Wkly Rep. 1993;42:59798336690Centers for Disease Control and Prevention Staphylococcus aureus resistant to vancomycin¾United States, 2002. MMWR Morb Mortal Wkly Rep. 2002;51:565712139181Chang S, Sievert DM, Hageman JC, Boulton ML, Tenover FC, Downes FP, Infection with vancomycin-resistant Staphylococcus aureus containing the vanA resistance gene. N Engl J Med. 2003;348:13427 10.1056/NEJMoa02502512672861Centers for Disease Control and Prevention Recommendations for preventing the spread of vancomycin resistance. Recommendations of the Hospital Infection Control Practices Advisory Committee (HICPAC). MMWR Recomm Rep. 1995;44:1137565541Shlaes DM, Gerding DN, John JF Jr, Craig WA, Bornstein DL, Duncan RA, Society for Healthcare Epidemiology of America and Infectious Disease Society of America Joint Committee on the Prevention of Antimicrobial Resistance: guidelines for the prevention of antimicrobial resistance in hospitals. Clin Infect Dis. 1997;18:27591Jarvis WR Preventing the emergence of multidrug-resistant microorganisms through antimicrobial use controls: the complexity of the problem. Infect Control Hosp Epidemiol. 1996;17:4905 10.1086/6473488875291Gould IM A review of the role of antibiotic policies in the control of antibiotic resistance. J Antimicrob Chemother. 1999;43:45965 10.1093/jac/43.4.45910350373Hamilton CD, Drew R, Janning S, Latour JK, Hayward S Excessive use of vancomycin: a successful intervention strategy at an academic medical center. Infect Control Hosp Epidemiol. 2000;21:425 10.1086/50170310656355Singer MV, Haft R, Barlam T, Aronson M, Shafer A, Sands KE Vancomycin control measures at a tertiary-care hospital: impact of interventions on volume and patterns of use. Infect Control Hosp Epidemiol. 1998;19:24853 10.1086/6478039605273Doern GV, Heilmann KP, Huynh HK, Rhomberg PR, Coffman SL, Brueggemann AB Antimicrobial resistance among clinical isolates of Streptococcus pneumoniae in the United States during 1999–2000, including a comparison of resistance rate since 1994–1995. Antimicrob Agents Chemother. 2001;45:17219 10.1128/AAC.45.6.1721-1729.200111353617Salgado CD, Farr BM, Calfee DP Community-acquired methicillin-resistant Staphylococcus aureus: a meta-analysis of prevalence and risk factors. Clin Infect Dis. 2003;36:1319 10.1086/34543612522744Tice AD, Rehm SJ, Dalovisio JR, Bradley JS, Martinelli LP, Graham DR, Practice guidelines for outpatient parenteral antimicrobial therapy. Clin Infect Dis. 2004;38:165172 10.1086/42093915227610Charlson ME, Pompei P, Ales KL, MacKenzie CR A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40:37383 10.1016/0021-9681(87)90171-83558716Deyo RA, Cherkin DC, Ciol MA Adapting a clinical comorbidity index for use with ICD-9 CM administrative databases. J Clin Epidemiol. 1992;6:6139 10.1016/0895-4356(92)90133-81607900Evans ME, Kortas KJ Vancomycin use in a university medical center: comparison with Hospital Infection Control Practices Advisory Committee guidelines. Infect Control Hosp Epidemiol. 1996;17:3569 10.1086/6473168805065Watanakunakorn C Prescribing pattern of vancomycin in a community teaching hospital with low prevalence of vancomycin resistant enterococci. Infect Control Hosp Epidemiol. 1997;18:7679 10.1086/6475339397372Roghmann MC, Perdue BD, Polish L Vancomycin use in a hospital with vancomycin restriction. Infect Control Hosp Epidemiol. 1999;20:603 10.1086/5015489927270Lipsky BA, Baker CA, McDonald LL, Suzuki NT Improving the appropriateness of vancomycin use by sequential interventions. Am J Infect Control. 1999;27:8491 10.1016/S0196-6553(99)70086-610196484Kwan T, Lin F, Ngai B, Loeb M Vancomycin use in 2 Ontario tertiary care hospitals: a survey. Clin Invest Med. 1999;22:2566410664867Jarvis WR Epidemiology, appropriateness, and cost of vancomycin use. Clin Infect Dis. 1998;26:12003 10.1086/5202849597253Sinkowitz RL, Keyserling H, Walker TJ, Holland J, Jarvis WR Epidemiology of vancomycin usage at a children's hospital, 1993 through 1995. Pediatr Infect Dis J. 1997;16:4859 10.1097/00006454-199705000-000069154542Paskovaty A, Pflomm JM, Myke N, Seo SK A multidisciplinary approach to antimicrobial stewardship: evolution into the 21st century. Int J Antimicrob Agents. 2005;25:110 10.1016/j.ijantimicag.2004.09.00115620820Classen DC, Burke JP, Wenzel RP Infectious diseases consultation: impact on outcomes for hospitalized patients and results of a preliminary study. Clin Infect Dis. 1997;24:46870 10.1093/clinids/24.3.4689114202Byl B, Clevenbergh P, Jacobs F, Struelens MJ, Zech F, Kentos A, Impact of infectious diseases specialists and microbiological data on the appropriateness of antimicrobial therapy for bacteremia. Clin Infect Dis. 1999;29:606 10.1086/52018210433566Lee CE, Zembower TR, Fotis MA, Postelnick MJ, Greenberger PA, Peterson LR, The incidence of antimicrobial allergies in hospitalized patients: implications regarding prescribing patterns and emerging bacterial resistance. Arch Intern Med. 2000;160:281922 10.1001/archinte.160.18.281911025792Tice AD, Hoaglund PA, Nolet B, McKinnon PS, Mozaffari E Cost perspectives for outpatient intravenous antimicrobial therapy. Pharmacotherapy. 2002;22:63S70S 10.1592/phco.22.4.63S.3365311837549