Accurate prediction equations for ventilatory thresholds in cardiometabolic disease when gas exchange analysis is unavailable: development and validation

医学 通气阈值 指南 运动处方 内科学 组内相关 心脏病学 代谢当量 物理疗法 心肺适能 心率 最大VO2 血压 体力活动 病理 临床心理学 心理测量学
作者
Juliana Goulart Prata Oliveira Milani,Maurício Milani,Felipe Vilaça Cavallari Machado,Matthias Wilhelm,Thimo Marcin,Flavio D’Ascenzi,Luna Cavigli,Charly Keytsman,Maarten Falter,Bruno Bonnechère,Raf Meesen,Fabrício Braga,Graziella França Bernardelli Cipriano,Véronique Cornelissen,Kenneth Verboven,Gerson Cipriano,Dominique Hansen
出处
期刊:European Journal of Preventive Cardiology [Oxford University Press]
卷期号:31 (16): 1914-1924 被引量:15
标识
DOI:10.1093/eurjpc/zwae149
摘要

AIMS: To develop and validate equations predicting heart rate (HR) at the first and second ventilatory thresholds (VTs) and an optimized range-adjusted prescription for patients with cardiometabolic disease (CMD). To compare their performance against guideline-based exercise intensity domains. METHODS AND RESULTS: Cross-sectional study involving 2868 CMD patients from nine countries. HR predictive equations for first and second VTs (VT1, VT2) were developed using multivariate linear regression with 975 cycle-ergometer cardiopulmonary exercise tests (CPET). 'Adjusted' percentages of peak HR (%HRpeak) and HR reserve (%HRR) were derived from this group. External validation with 1893 CPET (cycle-ergometer or treadmill) assessed accuracy, agreement, and reliability against guideline-based %HRpeak and %HRR prescriptions using mean absolute percentage error (MAPE), Bland-Altman analyses, intraclass correlation coefficients (ICC). HR predictive equations (R²: 0.77 VT1, 0.88 VT2) and adjusted %HRR (VT1: 42%, VT2: 77%) were developed. External validation demonstrated superiority over widely used guideline-directed intensity domains for %HRpeak and %HRR. The new methods showed consistent performance across both VTs with lower MAPE (VT1: 7.1%, VT2: 5.0%), 'good' ICC for VT1 (0.81, 0.82) and 'excellent' for VT2 (0.93). Guideline-based exercise intensity domains had higher MAPE (VT1: 6.8-21.3%, VT2: 5.1-16.7%), 'poor' to 'good' ICC for VT1, and 'poor' to 'excellent' for VT2, indicating inconsistencies related to specific VTs across guidelines. CONCLUSION: Developed and validated HR predictive equations and the optimized %HRR for CMD patients for determining VT1 and VT2 outperformed the guideline-based exercise intensity domains and showed ergometer interchangeability. They offer a superior alternative for prescribing moderate intensity exercise when CPET is unavailable.
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