Acute Myocardial Infarction, unspecified
Conditions
Interventions
After the person's approach and their agreement to participate in the research, their chart will be consulted and there will be a dialogue between the researcher and the participant to confirm the inc
Procedure/surgery
H02.010.625
Sponsors
Universidade Federal do Triângulo Mineiro - UFTM
Universidade Federal do Triângulo Mineiro - UFTM
Eligibility
Age
18 Years to 90 Years
Inclusion criteria
Inclusion criteria: Patients hospitalized at the Coronary Intensive Care Unit of the HC - UFTM;Patients of both sexes, with age greater than or equal to 18 years; Medical diagnosis of uncomplicated AMI (Killip I and II) with electrocardiogram (ECG) with or without ST segment elevation (successfully submitted to PTCA with residual stenosis of less than 50%).Have a sufficient level of understanding to understand the exercises to be performed (assessed by the Glasgow Coma Scale: score 3 to 15);Agree to participate in the research - signing the Term of Consent
Exclusion criteria
Exclusion criteria: Patients with a history of previous MI, complicated MI (Killip III and IV); Signs and / or symptoms consistent with angina after AMI or reinfarction; Persistent anomalous pressure behavior (refractory hypertension with levels above 180 / 110mmHg); Atrial fibrillation; Malignant ventricular arrhythmias; Complex ventricular extrasystoles; Supraventricular or sinus tachycardia (greater than 120 beats per minute); Atrioventricular block of 2nd or 3rd degree; Implantation of pacemaker; Signs of low output or ventricular failure; Hypotension; Febrile state; Respiratory failure; Sequence of stroke; Lower limb amputation; Severe aortic stenosis; Left coronary trunk lesion> 50%; Previous surgery of myocardial revascularization; Impossibility of progression in the protocol and hospital admission after 48 hours of the initiation of AMI
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increase in HRV, reducing cardiovascular risks and / or occurrence of new coronary events. Statistical analysis will be performed comparing HRV in GC and GMP. Numerical variables will be measured with central tendency and dispersion (standard deviation, mean, median and interquartile ranges). Considering Student's t test for the sample matched to the normality criteria by Kolmogorov-Smirnov 2009 (p?0.05) and homogeneity of the variance by Levene test ((p?0.05).) In case of violation of the principles, the test will be applied non-parametric Wilcoxon-Mann-Whitney test | — |
Secondary
| Measure | Time frame |
|---|---|
| Greater functionality to these individuals; The numerical variables will be performed measures of central tendency and dispersion (standard and mean deviation);Reduce the length of hospital stay (Intensive Care Unit and Infirmary). Numerical variables will be performed measures of central tendency and dispersion (standard and mean deviation) | — |
Countries
Brazil
Contacts
Public ContactGraziella Paula;Graziella Paula Neri;Neri
Universidade Federal do Triângulo Mineiro - UFTM;Universidade Federal do Triângulo Mineiro - UFTM
Outcome results
None listed