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Pharmaceutical Care in the Reduction of Readmission Rates in Diabetes Melitus

Not Applicable
Completed
Conditions
Diabetes Mellitus
Interventions
Behavioral: Structured pharmaceutical care
Behavioral: Comparator
Registration Number
NCT03786978
Lead Sponsor
Hospital de Clinicas de Porto Alegre
Brief Summary

Diabetes mellitus (DM) is associated with the frequent use of polypharmacy at different times of administration and requires special attention from the patient or caregivers in order to properly treatment performed. The degree of Functional Literacy in Health is defined as the ability to apply literacy skills to health-related materials, including prescriptions, package inserts, and home care instructions. Several questionnaires are used in research and clinical practice to assess the pronunciation and understanding of commonly used medical terms, as the SAHLPA-18 (Short Assessment of Health Literacy for Portuguese Speaking Adults). The Brief Medication Questionnaire (BMQ) evaluates adherence to medication use from a patient's perspective.

During the basal visit, after the characterization of the sample (n= 100), inpatients from Hospital de Clínicas de Porto Alegre (HCPA) were randomized to interventional or comparator group. The interventional group was follow up during a year after basal discharge. Comparator group received only a phone call, 30 days after the basal discharge, to question how was their healthy status. Readmission rates were evaluated for both groups. Also, a economic evaluation was made to measure the readmission rates in terms of costs.

Detailed Description

The first outcome of the clinical study was to measure the readmission rate through a structured pharmaceutical care model after basal hospital discharge and measure the effect of this intervention in terms of readmission reduction in a short term period of 30 days, regardless of the hospitalization reason.

As secondary outcomes the investigators measured the readmission rates after basal hospital discharge and the effect of the intervention in terms of readmission reduction in 60, 90,180 and 365 days after basal hospital discharge. Also, the readmission costs in terms of cost-effectiveness were evaluate.

The sample consisted of 100 patients with DM associated with other comorbidities, hospitalized for any reason in the HCPA, of both sexes, older than 18 years.

Informed consent, demographic and validated questionnaires data were collected in the basal visit. After that, patients were randomized to:

Group 1: comparator; Group 2: structured pharmaceutical intervention.

Seven days after basal hospital discharge, drugs adherence was verified.

The interventional group received pharmaceutical care at basal hospitalization stay, after randomization, have their prescription reviewed until 7 days after discharge of basal hospitalization and also received structured phone calls and mobile SMS (Short Message Service) during one year follow up (30, 60, 180 and 365 days).

Electronic medical records of the included patients (intervention and comparator groups) were reviewed monthly for 12 months, aiming to identify access to emergency services or hospital readmissions at the HCPA and, consequently, the reasons for readmissions and outcomes.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Patients with DM and other comorbidities hospitalized for any reason at HCPA
  • Patients who are literate or have a literate caregiver;
  • Signature in the Term of Consent.
Exclusion Criteria
  • Limited ability to communicate and read in Portuguese and absence of responsible caregiver at the patient room;
  • Neuropsychiatric diseases (psychosis, delirium or severe dementia);
  • Terminal illness;
  • Transplanted patients or users of warfarin, as these patients receive formal guidance from the HCPA pharmaceutical team;
  • Auditory or visual impairment that, at the discretion of the investigator, prevents the patient from participating in the study;
  • Do not have own mobile number or a close family member living in the same household.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Structured pharmaceutical careStructured pharmaceutical carePatients receive a structured pharmaceutical care until one year after hospital discharge
Comparator groupComparatorPatient received a single phone call 30 days after basal hospital discharge.
Primary Outcome Measures
NameTimeMethod
Short term readmission rate30 days after basal hospital discharge

Hospital readmissions after basal hospital discharge

Secondary Outcome Measures
NameTimeMethod
Long term readmission rate- 365 days365 days after basal hospital discharge

Hospital readmissions after basal hospital discharge

Readmission rate - 60 days60 days after basal hospital discharge

Hospital readmissions after basal hospital discharge

Readmission rate - 90 days90 days after basal hospital discharge

Hospital readmissions after basal hospital discharge

Long term readmission rate- 180 days180 days after basal hospital discharge

Hospital readmissions after basal hospital discharge

Economic evaluation365 days

Comparison between costs from readmission in both randomized groups

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