Pemulihan jantung berasaskan senaman untuk orang dewasa dengan fibrilasi atrium

Mesej utama

• Pemulihan jantung berasaskan senaman mungkin boleh menambahbaik gejala dan kualiti hidup serta mungkin dapat menambahbaik kapasiti senaman (jumlah maksimum usaha fizikal yang dapat dilakukan oleh seseorang) dalam kalangan orang dewasa dengan fibrilasi atrium (AF).

• Tidak ada bukti yang mencukupi untuk mengetahui kesan senaman terhadap kematian atau kesan serius yang tidak diingini.

• Kualiti bukti adalah sederhana hingga sangat rendah. Lebih banyak penyelidikan berkualiti tinggi diperlukan.

Apakah fibrilasi atrium?

Fibrilasi atrium (AF) adalah ritma jantung yang tidak teratur. Ia boleh meningkatkan risiko seseorang terhadap strok dan komplikasi lain berkaitan jantung. Gejala AF termasuklah berdebar-debar, keletihan, dan pening. Senaman mungkin boleh membantu orang dengan AF, kerana ia memberi kesan terhadap kesihatan jantung dan kesejahteraan keseluruhan.

Apakah yang ingin kami ketahui?

Kami melihat kepada faedah dan kemungkinan mudarat dari pemulihan jantung berasaskan senaman untuk orang dewasa dengan AF.

Apakah yang kami lakukan?

Kami mencari kajian-kajian yang membandingkan pemulihan jantung berasaskan senaman dengan tanpa senaman dalam kalangan orang dengan AF. Kami ingin mengetahui kesan pada kematian, kesan serius yang tidak diingini, serta pelbagai ukuran keterukan AF dan kesejahteraan pesakit.

Apakah yang kami temui?

Kami menyertakan 20 kajian melibatkan sejumlah 2039 orang dengan AF. Secara keseluruhan, terdapat 101 kematian dan 28 kesan serius yang tidak diingini. Tidak ada bukti yang mencukupi untuk mengetahui sama ada pemulihan jantung berasaskan senaman dapat mengurangkan risiko kematian atau kesan serius yang tidak diingini. Pemulihan berasaskan senaman mungkin dapat mengurangkan pengulangan AF, gejala AF, dan mungkin menambahbaik kualiti hidup dari aspek mental. Pemulihan jantung berasaskan senaman juga mungkin boleh mengurangkan keterukan gejala AF dan dapat menambahbaik kapasiti senaman.

Apakah batasan bukti?

Keyakinan kami terhadap penemuan keseluruhan ulasan ini adalah terhad kerana ada kemungkinan bahawa orang dalam kajian-kajian tersebut mengetahui rawatan mana yang mereka terima; pelaporan keputusan yang tidak lengkap; hasil yang berbeza-beza merentasi kajian; dan jumlah orang yang dimasukkan dalam kajian adalah agak kecil.

Sejauh manakah bukti ini terkini?

Bukti adalah terkini sehingga Mac 2024.

Kesimpulan Pengarang: 

Due to few randomised participants and typically short-term follow-up, the impact of ExCR on all-cause mortality or serious adverse events for people with AF is uncertain. ExCR likely improves AF-specific measures including reduced AF recurrence, symptom burden, and episode duration, as well as the mental components of HRQoL. ExCR may improve AF symptom severity, episode frequency, and VO 2puncak . Future high-quality RCTs are needed to assess the benefits of ExCR for people with AF on patient-relevant outcomes including AF symptom severity and burden, AF recurrence, AF-specific quality of life, and clinical events such as mortality, readmissions, and serious adverse events. High-quality trials are needed to investigate how AF subtype and clinical setting (i.e. primary and secondary care) may influence ExCR effectiveness.

Baca abstrak penuh ...
Latar Belakang: 

Atrial fibrillation (AF), the most prevalent cardiac arrhythmia, disrupts the heart's rhythm through numerous small re-entry circuits in the atrial tissue, leading to irregular atrial contractions. The condition poses significant health risks, including increased stroke risk, heart failure, and reduced quality of life. Given the complexity of AF and its growing incidence globally, exercise-based cardiac rehabilitation (ExCR) may provide additional benefits for people with AF or those undergoing routine treatment for the condition.

Matlamat: 

To assess the benefits and harms of ExCR compared with non-exercise controls for people who currently have AF or who have been treated for AF.

Kaedah Pencarian: 

We searched the following electronic databases: CENTRAL in the Cochrane Library, MEDLINE Ovid, Embase Ovid, PsycINFO Ovid, Web of Science Core Collection Thomson Reuters, CINAHL EBSCO, LILACS BIREME, and two clinical trial registers on 24 March 2024. We imposed no language restrictions.

Kriteria Pemilihan: 

We included randomised clinical trials (RCTs) that investigated ExCR interventions compared with any type of non-exercise control. We included adults 18 years of age or older with any subtype of AF or those who had received treatment for AF.

Pengumpulan Data dan Analisis: 

Five review authors independently screened and extracted data in duplicate. We assessed risk of bias using Cochrane's RoB 1 tool as outlined in the Cochrane Handbook for Systematic Reviews of Interventions . We assessed clinical and statistical heterogeneity by visual inspection of the forest plots and by using standard Chi² and I² statistics. We performed meta-analyses using random-effects models for continuous and dichotomised outcomes. We calculated standardised mean differences where different scales were used for the same outcome. We used the GRADE approach to assess the certainty of the evidence.

Keputusan Utama: 

We included 20 RCTs involving a total of 2039 participants with AF. All trials were conducted between 2006 and 2024, with a follow-up period ranging from eight weeks to five years. We assessed the certainty of evidence as moderate to very low. Five trials assessed comprehensive ExCR programmes, which included educational or psychological interventions, or both; the remaining 15 trials compared exercise-only cardiac rehabilitation with controls. The overall risk of bias in the included studies was mixed. Details on random sequence generation, allocation concealment, and use of intention-to-treat analysis were typically poorly reported.

Evidence from nine trials (n = 1173) suggested little to no difference in mortality between ExCR and non-exercise controls (risk ratio (RR) 1.06, 95% confidence interval (CI) 0.76 to 1.49; I² = 0%; 101 deaths; low-certainty evidence). Based on evidence from 10 trials (n = 825), ExCR may have little to no effect on SAEs (RR 1.30, 95% CI 0.63 to 2.67; I² = 0%; 28 events; low-certainty evidence). Evidence from four trials (n = 378) showed that ExCR likely reduced AF recurrence (measured via Holter monitoring) compared to controls (RR 0.70, 95% CI 0.56 to 0.88; I² = 2%; moderate-certainty evidence). ExCR may reduce AF symptom severity (mean difference (MD) −1.59, 95% CI −2.98 to −0.20; I² = 61%; n = 600; low-certainty evidence); likely reduces AF symptom burden (MD −1.61, 95% CI −2.76 to −0.45; I² = 0%; n = 317; moderate-certainty evidence); may reduce AF episode frequency (MD −1.29, 95% CI −2.50 to −0.07; I² = 75%; n = 368; low-certainty evidence); and likely reduces AF episode duration (MD −0.58, 95% CI −1.14 to −0.03; I² = 0%; n = 317; moderate-certainty evidence), measured via the AF Severity Scale (AFSS) questionnaire. Moderate-certainty evidence from six trials (n = 504) showed that ExCR likely improved the mental component summary measure in health-related quality of life (HRQoL) of the 36-item Short Form Health Survey (SF-36) (MD 2.66, 95% CI 1.22 to 4.11; I² = 2%), but the effect of ExCR on the physical component summary measure was very uncertain (MD 1.75, 95% CI −0.31 to 3.81; I² = 52%; very low-certainty evidence). ExCR also may improve individual components of HRQoL (general health, vitality, emotional role functioning, and mental health) and exercise capacity (peak oxygen uptake (VO 2puncak ) and 6-minute walk test) following ExCR. The effects of ExCR on serious adverse events and exercise capacity were consistent across different models of ExCR delivery: centre compared to home-based, exercise dose, exercise only compared to comprehensive programmes, and aerobic training alone compared to aerobic plus resistance programmes. Using univariate meta-regression, there was evidence of significant association between location of trial and length of longest follow-up on exercise capacity.

Nota terjemahan: 

Sila hubungi cochrane@rumc.edu.my untuk sebarang pertanyaan berkaitan terjemahan ini. Diterjemah oleh Syed Amirfaiz (Universiti Islam Antarabangsa Malaysia Kuantan). Disunting oleh Shazlin Shaharudin (Universiti Sains Malaysia).

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