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临床试验/NCT03522909
NCT03522909已完成不适用

The Center for Peripartum Optimization: An Innovative Approach to Care Coordination

Johns Hopkins University1 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2017年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
250
试验地点
1
主要终点
Hospital length of stay

研究概览

简要总结

In January 2017 investigators started a Center for Peripartum Optimization (CPO) with the aim of optimizing a patient's clinical status in an outpatient setting to minimize unnecessary laboratory tests and studies, costly inpatient consultations, the likelihood of post-surgical adverse events, escalations in level of care, inpatient admissions and readmissions. This research project seeks to evaluate the impact of this innovative concept on patient outcomes during the last 12 months. Investigators will accomplish this by collecting retrospective data from patients' electronic medical records in the intervention group and comparing it to data gathered from a controlled group of patients with similar comorbidities but who were not evaluated at the CPO clinic.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
— 至 60 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Records of all female, obstetric patients of child-bearing age who were evaluated in the Center for Peripartum Optimization during the period between January 2017 and January
  • Controlled group will include parturients with match high risk comorbidities or history of nonobstetric surgery during pregnancy who delivered at Johns Hopkins Hospital (JHH) during July 1, 2016 - Dec 31, 2016
  • Patients with any one or more of these high risk comorbidities:
  • Complex spine pathologies (Scoliosis, vertebral fusion, disc disease, spinal canal defects, neuropathies, and nerve disease, etc.)
  • Neurological pathology (Cerebral ischemia, tumor, increased intracranial pressure, cerebral vascular disease, etc.)
  • Cardiac disease (Congenital, valvular, pulmonary hypertension, cardiomyopathy, ischemic disease, arrhythmia, etc.)
  • Pulmonary disease (History of pulmonary embolism, interstitial lung disease, severe asthma, cancer, etc.)
  • Morbid Obesity (Obstructive Sleep Apnea, equipment considerations)
  • Hematologic Disorders (Thrombophilias, coagulopathies, patients on anticoagulation)
  • Abnormal placentation (Previa, accreta / increta / percreta)
  • Anesthetic concerns (Airway abnormalities, history of adverse anesthetic reactions or experiences (i.e. recall, anaphylaxis))
  • Fetal therapy patients requiring specialized management (Ex utero intrapartum treatment (EXIT), Fetoscopic endotracheal occlusion (FETO), Twin-to-twin transfusion syndrome (TTTS), Percutaneous Umbilical Blood Sampling (PUBS), etc.)
  • Chronic Pain

排除标准

  • Records of CPO participating parturients outside the specified timeframe.
  • Records of obstetric patients of child-bearing age without high-risk comorbid conditions described in inclusion criteria.
  • Records of patients seen in CPO clinic that did not deliver at our institution

结局指标

主要结局

Hospital length of stay

时间窗: 1 year

Total days of hospital admission

次要结局

  • Number of admissions from outside hospitals(1 year)
  • Patient satisfaction(1 year)
  • Opioids use(1 year)
  • Cost of outpatient care(1 year)
  • Cost of inpatient admission(1 year)
  • ICU admissions(1 year)
  • Neonatal Intensive Care Unit (NICU) admissions(1 year)
  • Hospital readmissions rate(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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