Impact of a Technology Platform Based on Enhanced Recovery After(ERAS) Surgery on Length of Stay After Coronary Artery Bypass Grafting: Timely Project
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: ERACS with Digital Platform.
- Who it may be relevant to
- Registry conditions: ERAS, Cardiac Surgery, Cardiac Surgery-CABG, Digital Health. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Brazil
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Estudo Randomizado de Cluster Escalonado Para Avaliar o Impacto de Uma Plataforma tecnológica Baseada no ERAS (Enhanced Recovery After Surgery) no Tempo de permanência após Cirurgia de revascularização miocárdica: Projeto Tempos Certos - REPLICCAR III
Overview
Cardiovascular diseases continue to be the leading cause of death worldwide. Among them, coronary artery disease has the greatest impact, being characterized as one of the main causes of death in Brazil over the last decade. One of the well-established treatments is coronary artery bypass grafting, which is the most performed among cardiac surgeries and, in our scenario, is primarily funded by the Unified Health System (SUS). The information obtained from the Paulista Registry of Cardiovascular Surgeries (REPLICCAR), in partnership with FAPESP, has been important for implementing improvements in the landscape of cardiac surgeries in the state of São Paulo. Although outcomes in cardiac surgery have improved due to the structuring and organization of quality programs, this is still not a reality at the national level. In a situation where data collection and quality initiatives play a central role in continuous improvement, generating value becomes essential for the sustainability of cardiac surgery programs. In this sense, the concept of Enhanced Recovery After Surgery (ERAS) has gained increasing traction. This concept is based on multidisciplinary protocols and scientific evidence, which help prepare patients for rapid recovery, resulting in reduced complications, shorter hospital stays, and, primarily, lower hospital costs. On the other hand, the increase in surgical waiting lists has also led to a rise in home mortality due to cardiac causes. Thus, among the various challenges imposed by the current scenario, the investigators believe that preparing patients for rapid recovery after coronary artery bypass grafting presents an opportunity for the sustainability of the healthcare system. Therefore, the aim of this project is to evaluate the impact of a technology platform based on ERAS on the postoperative recovery time of patients undergoing coronary artery bypass grafting in reference centers in the state of São Paulo, Timely Project - REPLICCAR III.
Interventions
- Other ERACS with Digital Platform
The assistance provided to patients in the intervention group will be sequential and prospective. The project will utilize an app based on protocols that prepare patients for rapid recovery (ERAS), starting before surgery and extending up to 30 days post-discharge. This includes pre-operative evaluations (psychological, nutritional, and others), scheduling and confirming hospital admission, and following specific protocols during surgery and intensive care. The app aims to enhance communication
Primary outcome measures
- Lenght of Stay [Time frame: up to 30 days after surgery]
Secondary outcome measures (4)
- Percentage of Completeness of Protocol Steps [Time frame: up to 01 week after surgery.]
- Morbility and Mortality [Time frame: up to 6 months after surgery]
- Patient-reported outcomes (PROM) [Time frame: up to 6 months after surgery]
- Patient reported experience measure(PREM) [Time frame: up to 6 months after surgery]
Eligibility criteria
Inclusion criteria
- Adults over 18 years old
- Indication for primary isolated CABG (elective or urgent status)
- Own a personal cell phone
- Have internet access
- Knowledgeable in using the device
- Full understanding and agreement regarding the informed consent form (ICF)
Exclusion criteria
- Indication for associated surgery
- Glycosylated hemoglobin level greater than 8%
- Creatinine clearance less than 30 mL/min
- Pre-operative atrial fibrillation or use of pre-operative anticoagulation
- Hemoglobin less than 12 g/dL
- Users of illicit drugs
- STS score greater than 4%
- Physical or mental disabilities that prevent adherence to the protocol
- Refusal by the patient or family member
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Health services research
Study locations
Brazil · 2 centers
- InCor - Instituto do Coração do Hospital das Clínicas da FMUSP — São Paulo
- InCor - Instituto do Coração do Hospital das Clínicas da FMUSP — São Paulo
Publications
- Borgomoni GB, Reis PH, Pinheiro G, Ribas FF, Silva GSD, Campagnucci VP, Issa M, Farsky PS, Barg MM, Tiveron MG, Dos Reis Falcao LF, Dias RD, Ferreira Lisboa LA, Jatene FB, Mejia OAV. The technological proposal based on enhanced recovery after cardiac surgery for changing traditional care in Latin America: REPLICCAR III Study Protocol. PLoS One. 2025 Dec 31;20(12):e0338301. doi: 10.1371/journal.pon PMID 41474739
Identifiers
NCT: NCT06786819 · 5811/24/022