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N/A N=631 Randomized Single-blind Health Services Research

Value of Technology to Transfer Discharge Information

Information Dissemination · Interprofessional Relations

Enrolled (actual)
631
Serious AEs
3.2%
Results posted
May 2012
Primary outcome: Primary: Hospital Readmission, at Least One — 117; 119; 199; 196 participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Discharge communication software (Device); Usual care discharge process (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Agency for Healthcare Research and Quality (AHRQ)
Primary completion
Aug 2007

Outcome Measures

OutcomeResultp-value
PRIMARY
Hospital Readmission, at Least One
117; 119; 199; 196
SECONDARY
Patients' Perception of Discharge Process, Effectiveness, Satisfaction, Preparedness
SECONDARY
Patients' Perception of Discharge Process, Satisfaction
SECONDARY
Pharmacist Needed to Clarify the Discharge Prescription
SECONDARY
Pharmacist's Satisfaction With Discharge Prescription
SECONDARY
At Least One Adverse Event Within One Month After Discharge
23; 23; 293; 292
SECONDARY
Patient's Satisfaction With Drug Information
SECONDARY
Primary Care Physician's Perception, Effectiveness
SECONDARY
Primary Care Physician's Perception, Satisfaction
SECONDARY
Discharge Physician Satisfaction With Discharge Process
SECONDARY
Number of Outpatient Visits
SECONDARY
Number of Emergency Department Visits
112; 128; 204; 187
SECONDARY
Physician Time Spent to Complete the Discharge Application

Summary

The transition from hospital to home is a high-risk period in a patient's illness. Poor communication between healthcare providers at hospital discharge is common and contributes to adverse events affecting patients after discharge. The importance of good communication at discharge will increase as more primary care providers delegate inpatient care to hospitalists. Any process that improves information transfer among providers at discharge might improve the health and safety of patients discharged from U.S. hospitals each year, and to appreciably reduce unnecessary healthcare expenditures. Information transfer among healthcare providers and their patients can be undermined because of inaccuracies, omissions, illegibility, logistical failure (e.g., information is never delivered), and delays in generation (i.e., dictation or transcription) or transmission. Root causes include recall error, increased physician workloads, interface failures (e.g., physician-clerical) and poor training of physicians in the discharge process. Many of the deficiencies in the current process of information transfer at hospital discharge could be effectively addressed by the application of information technology. The proposed study will measure the value of a software application to facilitate information transfer at hospital discharge. The study is designed to compare the benefits of discharge health information technology versus usual care in high-risk patients recently discharged from acute care hospitalization. The design is a randomized, single-blind, controlled trial. The outcomes are readmission within 6 months, adverse events, and effectiveness and satisfaction with the discharge process from the patient and physician perspectives. The cost outcome is the physician time required to use the discharge software.

Eligibility Criteria

Inclusion Criteria

  • Inpatients at OSF Saint Francis Medical Center
  • Discharged by the hospitalist service or other inpatient services
  • High risk for poor post-discharge outcomes defined as probability of readmission (PRA) 0.4 or above

Exclusion Criteria

  • Less than 18 years old
  • Unwilling or unable to provide written consent
  • Life expectancy less than 6 months
  • Will receive outpatient care from a primary care physician who is the same as the discharging physician
  • Do not speak English or Spanish
  • Not alert and oriented when admitted
  • Do not have telephone for post-discharge contact
  • Do not reside in Central Illinois
  • Will be discharged to a nursing home
  • Previously enrolled as subjects in the trial
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00101868). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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