跳至主要内容
临床试验/NCT03372941
NCT03372941终止4 期

Hospital Avoidance Strategies for Treatment of Acute Bacterial Skin and Skin Structure Infection (ABSSSI)

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2019年3月4日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
终止
入组人数
11
试验地点
1
主要终点
Healthcare Utilization Related to ABSSSI

研究概览

简要总结

More than 40% of patients presenting with acute bacterial skin and skin structure infection (ABSSSI) to the Barnes-Jewish Hospital (BJH) emergency department (ED) are admitted for intravenous antibiotics. There is growing evidence to suggest that many hospital admissions for uncomplicated ABSSSI due to Gram-positive bacteria could be avoided with an alternative treatment strategy employing newer long-acting antibiotics. Coupled with close outpatient follow-up, such an alternative hospital avoidance strategy has the potential to improve quality and value of care for patients with uncomplicated ABSSSI and optimize use of limited inpatient healthcare resources.

详细描述

This study seeks to establish the feasibility and acceptability of an alternative treatment strategy for uncomplicated acute bacterial skin and skin structure infection (ABSSSI) in the Barnes Jewish Hospital (BJH) Emergency Department (ED) focusing on hospital admission avoidance using single-dose, long-acting antimicrobial therapy complemented by close follow-up in the ambulatory setting. The extended half-life of these new antimicrobials (dalbavancin, oritavancin) allows for an effective treatment course of >7 days with a single dose, which is the accepted duration for which ABSSSI is usually treated with daily doses of other intravenous or oral antimicrobials. The investigators believe that such an approach will conserve hospital resources by reducing admissions for uncomplicated ABSSSI while delivering comparable if not superior care for this disease, allowing optimal utilization of BJH inpatient beds for other serious medical conditions requiring inpatient care. The investigators believe this novel alternative approach will allow hospitals such as BJH to more cost-effectively and efficiently manage ABSSSI patients. This study will reduce the number of >2 midnight observation admissions to BJH for ABSSSI, thereby improving inpatient capacity to care for patients requiring >2 midnight hospital inpatient admission.

The investigators will conduct a randomized controlled trial comparing patients treated with a single-dose of intravenous dalbavancin (an antibiotic that has been FDA-approved for the treatment of ABSSSI and is currently being used in clinical practice in the U.S.) and discharged home from the ED with close ambulatory care follow-up in clinic vs. patients treated with "usual care" (hospital admission for multiple doses of intravenous vancomycin or other antibiotic directed towards Gram-positive bacteria). Clinical outcomes, healthcare utilization, hospital costs, and patient satisfaction will be evaluated.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult (age ≥18 years)
  • Diagnosis of uncomplicated ABSSSI suspected to be due to Gram-positive bacteria by treating ED clinician, with presence of the following:
  • Skin lesion size ≥75 cm2 (measured by area of erythema, edema, and/or induration) AND
  • Signs of systemic inflammation (at least 1 of the following: WBC >12,000 or <4,000 cells/mm3; ≥10% immature neutrophils on peripheral smear; temperature >38.3˚C or <36˚C; heart rate >90 bpm, respiratory rate >20 bpm). Signs of systemic inflammation not required if the patient is age >70 years, has diabetes mellitus, or has been treated with immunosuppressive or chemotherapy in the past 90 days.
  • Clinical determination by treating ED clinician that patient will need hospital admission for the sole purpose of receiving intravenous antibiotics directed only towards Gram-positive bacteria (e.g., vancomycin, cefazolin) to treat uncomplicated ABSSSI

排除标准

  • Risk for ABSSSI due to Gram-negative bacteria (neutropenia with absolute neutrophil count <500 cells/µL, HIV or severely immunocompromised, burns, infection after trauma or as a result of an aquatic environment, infection after skin graft)
  • Any abscess requiring bedside or operative drainage
  • Infection due to a vascular catheter or prosthetic device
  • Infection of a diabetic foot ulcer or decubitus ulcer
  • Necrotizing soft tissue infection
  • Sepsis (quick SOFA score ≥2) or septic shock (requiring vasopressors to maintain mean arterial pressure ≥65 mmHg despite resuscitation with at least 30mL/kg of IV crystalloid within first 3 hours)
  • Recent antibiotics in prior 14 days
  • Hypersensitivity to glycopeptides (vancomycin, televancin, dalbavancin, oritavancin)
  • Severe renal insufficiency (CrCl <30 mL/min)
  • Severe hepatic insufficiency (Child-Pugh Class C)
  • Pregnant or nursing

研究组 & 干预措施

Alternative treatment strategy

Active Comparator

Patient will receive a single dose of dalbavancin administered in the BJH ED or ED observation unit for ABSSSI followed by discharge w/ close Infectious Disease outpatient clinic follow-up.

干预措施: Dalbavancin (Drug)

结局指标

主要结局

Healthcare Utilization Related to ABSSSI

时间窗: 28 days

Repeat ED visit(s) within 28 days, need for hospital admission(s) to receive intravenous antibiotics ("alternative treatment strategy" arm), or need for switch to different oral or intravenous antibiotic to treat ABSSSI ("usual care" arm)

次要结局

  • Clinical Response(28 days)
  • Patient Satisfaction Specific to ABSSSI Care(28 days)
  • Clinical Success(28 days)
  • Overall Patient Satisfaction Based on Standardized Measures(28 days)
  • Patient Safety(28 days)
  • Healthcare Cost Related to ABSSSI Management(28 days)
  • Quality of Life Measured Using RAND SF-36 Survey(28 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Stephen Liang

Principal investigator

Washington University School of Medicine

研究点 (1)

Loading locations...

相似试验