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The Center for Peripartum Optimization

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03522909
Enrollment
250
Registered
2018-05-11
Start date
2017-01-31
Completion date
2020-12-31
Last updated
2021-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Communication, High Risk Pregnancy, Multidisciplinary Communication, Obstetric Complication

Keywords

obstetric anesthesia, telemedicine

Brief summary

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.

Interventions

OTHERSeen in clinic

We will be doing a retrospective chart review of patients seen in the Center for Peripartum Optimization to look for: 1. Primary outcome variable. \- Hospital length of stay 2. Secondary outcome variables. * Number of admissions from outside hospitals * Adverse outcomes * Intensive Care Unit admissions * Opioid use * NICU admissions * Patient satisfaction * Cost of inpatient admission * Cost of outpatient care * Hospital readmissions rate

Sponsors

Johns Hopkins University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
No minimum to 60 Years
Healthy volunteers
No

Inclusion criteria

* 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 2018. * 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) * Cancer * 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Hospital length of stay1 yearTotal days of hospital admission

Secondary

MeasureTime frameDescription
ICU admissions1 yearWhether patient needed ICU admission or transfer
Opioids use1 yearTo determine if patient require opioid use
Neonatal Intensive Care Unit (NICU) admissions1 yearNumber of times a neonate got admitted to the NICU
Number of admissions from outside hospitals1 yearThe total number of admissions to any other hospitals prior to admission or after discharge
Cost of inpatient admission1 yearthe entire admission cost of admission during hospital stay
Cost of outpatient care1 yearThe cost for outpatient care incurred by patient
Hospital readmissions rate1 yearThe number of times a patient got readmitted after discharge
Patient satisfaction1 yearWhether patient was satisfied (yes/no) with treatment course based on survey filled out by patient.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026