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3.
J Am Pharm Assoc (2003) ; 55(3): 246-54, 2015.
Article in English | MEDLINE | ID: mdl-26003155

ABSTRACT

OBJECTIVES: To determine if a community pharmacy-based transition of care (TOC) program that included the full scope of medication therapy management (MTM) services (TransitionRx) decreased hospital readmissions, resolved medication-related problems, and increased patient satisfaction. DESIGN: Prospective, quasi-experimental study. SETTING: Nine Kroger Pharmacies located in Western Cincinnati. PATIENTS: Patients older than 18 years of age and discharged from two local hospitals with a diagnosis of congestive heart failure, chronic obstructive pulmonary disease, or pneumonia. Patients were recruited from two local hospitals and referred to the community pharmacy for MTM services with the pharmacist within 1 week of discharge. MAIN OUTCOME MEASURES: Pharmacists reconciled the patients' medications, identified drug therapy problems, recommended changes to therapy, and provided self-management education. At 30 days after discharge, research personnel conducted telephone surveys, using a previously validated survey instrument, to assess hospital readmissions and patient satisfaction. Pharmacist interventions and medication-related problems were documented. RESULTS: A total of 90 patients completed the study. Of these, 20% of patients in the usual care group were admitted to the hospital within 30 days compared with 6.9% of patients in the intervention group (P = 0.019). In the 30 patients who received MTM services from the pharmacist, 210 interventions were made. The overall mean patient satisfaction with the TOC process was not significantly different between patients who were seen by the pharmacist and those who were not seen by the pharmacist. CONCLUSION: Community pharmacies successfully collaborated with hospitals to develop a referral process for TOC interventions. Patients who received MTM services from the pharmacist experienced significantly fewer readmissions than patients who received usual care.


Subject(s)
Community Pharmacy Services/organization & administration , Continuity of Patient Care/organization & administration , Medication Therapy Management/organization & administration , Patient Readmission/statistics & numerical data , Aged , Female , Humans , Male , Middle Aged , Ohio , Program Evaluation
4.
Am J Health Syst Pharm ; 71(16): 1357-65, 2014 Aug 15.
Article in English | MEDLINE | ID: mdl-25074955

ABSTRACT

PURPOSE: This article discusses how to plan and implement an ambulatory care pharmacist service, how to integrate a hospital- or health-system-based service with the mission and operations of the institution, and how to help the institution meet its challenges related to quality improvement, continuity of care, and financial sustainability. SUMMARY: The steps in implementing an ambulatory care pharmacist service include (1) conducting a needs assessment, (2) aligning plans for the service with the mission and goals of the parent institution, (3) collaborating with patients and physicians, (4) standardizing the patient care process, (5) proposing the service, (6) attaining the necessary resources, (7) identifying stakeholders, (8) identifying applicable quality standards, (9) defining competency standards, (10) planning for service payment, and (11) monitoring outcomes. Ambulatory care pharmacists have current opportunities to become engaged with patient-centered medical homes, accountable care organizations, preventive and wellness programs, and continuity of care initiatives. Common barriers to the advancement of ambulatory care pharmacist services include lack of complete access to patient information, inadequate information technology, and lack of payment. CONCLUSION: Ambulatory care pharmacy practitioners must assertively promote appropriate medication use, provide patient-centered care, pursue integration with the patient care team, and seek appropriate recognition and compensation for the services they provide.


Subject(s)
Ambulatory Care/organization & administration , Health Care Reform , Pharmaceutical Services/organization & administration , Humans , Program Development , United States
7.
Pharmacotherapy ; 27(10): 1467-70, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17896903

ABSTRACT

A 39-year-old man with a history of deep vein thrombosis and septic arthritis of the left knee was treated with warfarin and cefazolin. Therapeutic prothrombin times and international normalized ratios (INRs) were maintained with warfarin 32 mg/week for approximately 1 month. When the patient's antibiotic regimen was changed from cefazolin to nafcillin 2 g every 4 hours, his INR declined significantly. His warfarin dosage had to be increased to a maximum of 88 mg/week to achieve a therapeutic INR. After completion of antibiotic therapy with nafcillin, the patient's warfarin requirements slowly declined over several weeks. A maintenance dosage of warfarin 42-48 mg/week was necessary after nafcillin discontinuation. Hepatic cytochrome P450 isoenzyme induction by nafcillin is likely the mechanism of a warfarin-nafcillin interaction. The usual onset of effect is within 1 week after starting nafcillin, and the offset of the effect is usually evident within 4 weeks after nafcillin discontinuation. In patients taking warfarin who are prescribed nafcillin, a 2-4-fold increase in the warfarin dose may be necessary, and clinicians should closely monitor INRs.


Subject(s)
International Normalized Ratio , Nafcillin/therapeutic use , Warfarin/therapeutic use , Adult , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/adverse effects , Anti-Bacterial Agents/therapeutic use , Anticoagulants/administration & dosage , Anticoagulants/adverse effects , Anticoagulants/therapeutic use , Drug Interactions , Humans , Male , Nafcillin/administration & dosage , Nafcillin/adverse effects , Venous Thrombosis/blood , Venous Thrombosis/drug therapy , Warfarin/administration & dosage , Warfarin/adverse effects
8.
Prog Cardiovasc Nurs ; 22(2): 97-100, 2007.
Article in English | MEDLINE | ID: mdl-17541320

ABSTRACT

A 79-year-old man with a history of deep vein thrombosis and pulmonary embolism received anticoagulation therapy with warfarin 5 mg daily for 8 months. He was diagnosed with osteomyelitis and underwent partial metatarsal resection of his right foot. After surgery, antibiotics were initiated, including ertapenem sodium 1 g intravenously every 24 hours, vancomycin 1400 mg intravenously every 24 hours, and rifampin 300 mg by mouth twice daily. Achieving a therapeutic level of anticoagulation was difficult despite escalating doses of warfarin, because of the interaction with rifampin. A 5- to 6-fold increase in warfarin dose was prescribed to reach therapeutic international normalized ratios (INRs), but even these increases were insufficient to maintain his INR in the therapeutic range. After rifampin was discontinued, warfarin doses were gradually reduced over the next 2 months. When concurrent warfarin-rifampin therapy is necessary, vigilant monitoring is imperative and significant increases in warfarin doses are likely.


Subject(s)
Antibiotics, Antitubercular/adverse effects , Anticoagulants/adverse effects , Rifampin/adverse effects , Warfarin/adverse effects , Aged , Drug Administration Schedule , Drug Interactions , Drug Monitoring , Humans , International Normalized Ratio , Male , Nursing Assessment , Osteomyelitis/complications , Osteomyelitis/drug therapy , Osteomyelitis/surgery , Postoperative Care , Pulmonary Embolism/complications , Pulmonary Embolism/drug therapy , Risk Assessment , Venous Thrombosis/complications , Venous Thrombosis/drug therapy
9.
Am J Health Syst Pharm ; 64(9): 945-51, 2007 May 01.
Article in English | MEDLINE | ID: mdl-17468149

ABSTRACT

PURPOSE: A methodological approach was developed to facilitate expansion of clinical pharmacist-managed anticoagulation services across an integrated health care delivery network. METHODS: A stepwise approach to the development and implementation of ambulatory care clinical pharmacy services was used to facilitate expansion of pharmacist-managed anticoagulation clinics in a university hospital setting and a community hospital within the same health network. RESULTS: The Health Alliance of Greater Cincinnati successfully created a care delivery model using clinical pharmacists to provide comprehensive anticoagulation management services at a university hospital and a community hospital. The incidence of thromboembolic events was significantly lower in the pharmacy anticoagulation service patients versus the patients in the usual care setting (p=0.005). A statistically significant decrease in minor bleeding events was observed in the pharmacist-managed group (p=0.038). Although a decrease in major bleeding events was observed, it was not statistically significant (p=0.075). International Normalized Ratio values of the patients managed by the pharmacy anticoagulation clinics were within the therapeutic range approximately 75% of the time. CONCLUSION: A stepwise approach to the development and implementation of ambulatory care clinical pharmacy services has facilitated the expansion of pharmacist-managed anticoagulation clinics across an integrated health system. This may serve as a valuable template for other systems as they strive to develop medication therapy management services.


Subject(s)
Anticoagulants/therapeutic use , Drug Monitoring/methods , Pharmacists , Pharmacy Service, Hospital/organization & administration , Thromboembolism/drug therapy , Ambulatory Care , Anticoagulants/adverse effects , Delivery of Health Care, Integrated , Female , Hemorrhage/chemically induced , Hemorrhage/prevention & control , Hospitals, Community , Hospitals, University , Humans , International Normalized Ratio , Male , Outpatient Clinics, Hospital , Professional Role
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