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1.
Am J Emerg Med ; 38(11): 2387-2390, 2020 11.
Article in English | MEDLINE | ID: mdl-33041118

ABSTRACT

OBJECTIVES: Return visits to the emergency department (ED) and subsequent readmissions are common for patients who are unable to fill their prescriptions. We sought to determine if dispensing medications to patients in an ED was a cost-effective way to decrease return ED visits and hospital admissions for skin and soft tissue infections (SSTIs). METHODS: A retrospective review of ED visits for SSTIs, during the 24 weeks before and after the implementation of a medication dispensing program, was conducted. Charts were analyzed for both ED return visits and hospital admissions within 7 days and 30 days of the initial ED visit. Return visits were further reviewed to determine if the clinical conditions on subsequent visits were related to the initial ED presentation. A cost analysis comparing the cost of treatment to cost savings for return visits was also performed. RESULTS: Before the implementation of the medication dispensing program, the return rate in 7 days for the same condition was 9.1% and the rate of admission was 2.8%. The return rate for the same condition in 8-30 days was 2.1% and the rate of admission was 1.0%. After the implementation of the medication dispensing program, the return rate for the same condition in 7 days was 8.0%, and the admission rate was 1.7%. The return rate for the same condition in 8-30 days was 0.8%, and the admission rate was 0%. The total cost of dispensed medications was $4050, while total cost savings were estimated to be $95,477. CONCLUSION: A medication dispensing program in the ED led to a reduction in return visits and admissions for SSTIs at both 7 days and 30 days. For a cost of only $4050, an estimated total of $95,477 was saved. A medication dispensing program is a cost-effective way to reduce return visits to the ED and subsequent admissions for certain conditions.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Delivery of Health Care/methods , Emergency Service, Hospital , Hospitalization/statistics & numerical data , Patient Readmission/statistics & numerical data , Pharmaceutical Services , Skin Diseases, Infectious/drug therapy , Soft Tissue Infections/drug therapy , Abscess/drug therapy , Cellulitis/drug therapy , Cephalexin/therapeutic use , Clindamycin/therapeutic use , Cost Savings , Cost-Benefit Analysis , Costs and Cost Analysis , Doxycycline/therapeutic use , Drug Costs , Health Expenditures , Health Services Accessibility , Hospitalization/economics , Humans , Medication Systems, Hospital , Patient Readmission/economics , Pilot Projects , Transportation , Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic use
2.
J Addict Med ; 16(5): 595-598, 2022.
Article in English | MEDLINE | ID: mdl-35020700

ABSTRACT

BACKGROUND: Xylazine is an alpha-2 adrenergic agonist commonly used as a large animal anesthetic. It is used as an adulterant in illicit opioids, and it is now well established that its synergistic effect with opioids increases lethality. The amount of xylazine adulterating illicit opioids is growing at an alarming rate, present in almost one-third of opioid overdose deaths reported in Philadelphia in 2019. Despite this, there are no reports considering the management of patients using xylazine chronically. In particular, there are no reported cases detailing the management of xylazine withdrawal or exploring the potential for ongoing treatment for those in recovery from xylazine use. CASE SUMMARY: We present the case of a 29 year old female with opioid use disorder and chronic xylazine use, admitted to the intensive care unit for treatment of chronic lower extremity wounds thought to be due to xylazine injection. Her xylazine withdrawal was managed with a combination of dexmedetomidine infusion, phenobarbital and tizanidine, later transitioned to clonidine. By hospital day 4 she was no longer experiencing withdrawal symptoms. She was transitioned from full-agonist opioids for pain to buprenorphine via a buprenorphine "micro-induction" and was ultimately discharged on buprenorphine, clonidine, and gabapentin on day 19 of admission. CLINICAL SIGNIFICANCE: This case illustrates a potential treatment pathway that allows for safe and comfortable xylazine withdrawal in hospitalized patients. It also provides an introduction into several medical concerns affecting this patient population specifically, including xylazine-mediated soft tissue wounds.


Subject(s)
Buprenorphine , Dexmedetomidine , Opioid-Related Disorders , Substance Withdrawal Syndrome , Adrenergic Agonists/therapeutic use , Analgesics, Opioid/therapeutic use , Animals , Buprenorphine/therapeutic use , Clonidine , Dexmedetomidine/therapeutic use , Female , Gabapentin/therapeutic use , Humans , Opioid-Related Disorders/drug therapy , Phenobarbital/therapeutic use , Substance Withdrawal Syndrome/drug therapy , Xylazine/therapeutic use
3.
West J Emerg Med ; 21(4): 906-908, 2020 Jul 10.
Article in English | MEDLINE | ID: mdl-32726263

ABSTRACT

INTRODUCTION: The Philadelphia Department of Public Health (PDPH) declared a public health emergency due to hepatitis A in August 2019. Our emergency department (ED) serves a population with many of the identified risk factors for hepatitis A transmission. This study examines the impact of an ED-based hepatitis A vaccination program, developed in partnership with the PDPH, on incidence of hepatitis A infection and hospital admission. METHODS: We conducted a retrospective review of all ED visits in the 12-week period centered around the implementation of the ED-based hepatitis A vaccination program. All adult patients presenting to the ED were offered vaccination, with vaccines supplied free of charge by the PDPH. We compared the incidence of diagnosis and of hospital admission for treatment of hepatitis A before and after implementation of the program. RESULTS: There were 10,033 total ED visits during the study period, with 5009 of them prior to the implementation of the vaccination program and 5024 after implementation. During the study period, 669 vaccines were administered. Before the vaccination program began, 73 patients were diagnosed with hepatitis A, of whom 67 were admitted. After implementation of the program, 38 patients were diagnosed with hepatitis A, of whom 31 were admitted. CONCLUSION: A partnership between an ED and the local public health department resulted in the vaccination of 669 patients in six weeks in the midst of an outbreak of a vaccine-preventable illness, with a corresponding drop in ED visits and hospital admission for acute hepatitis A.


Subject(s)
Emergency Service, Hospital/statistics & numerical data , Hepatitis A , Immunization Programs , Public Health/methods , Adult , Disease Outbreaks , Female , Hepatitis A/epidemiology , Hepatitis A/prevention & control , Humans , Immunization Programs/methods , Immunization Programs/organization & administration , Incidence , Male , Middle Aged , Outcome Assessment, Health Care , Philadelphia/epidemiology , Retrospective Studies , Risk Factors
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