Can Intermittent Hypoxic Conditioning Enhance the Benefits of Standard Long COVID-19 Rehabilitation?

IF 9.4 1区 医学 Q1 GERIATRICS & GERONTOLOGY
Tim Kambič, Tadej Debevec, Mitja Lainscak
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The greater risk and most severe symptoms of long COVID-19 were manifested in females aged 35–50 years, patients with comorbidities (type 2 diabetes, allergies, lung diseases, heart failure, chronic kidney disease and obesity) and in unvaccinated individuals [<span>2-5</span>]. Sarcopenia is highly prevalent in patients with long COVID-19, particularly after longer hospitalisation [<span>6</span>].</p><p>Long COVID-19 is a heterogeneous, systemic and multiorgan syndrome that has been associated with &gt; 200 different symptoms. The accumulation of SARS-CoV-2 in the tissues, dysregulated immune response, inflammation and endothelial dysfunction induce damage to pulmonary (lung fibrosis and alveolar epithelium injury), cardiovascular (peri-myocarditis, arterial inflammation, micro-thrombosis and coagulopathy), skeletal muscle (muscle fibre atrophy and disrupted mitochondrial function) [<span>7, 8</span>], neurological (postural orthostatic tachycardia and dysautonomia) and autoimmune (onset of autoimmune diseases) systems (Figure 1) [<span>2-4, 9</span>]. These impairments are primarily manifested as fatigue, cough, shortness of breath at rest and after exercise, exercise intolerance, chest pain, joint and muscle pain, cognitive impairments (dizziness, brain fog) and sleep disorders, along with other less frequent symptoms [<span>2-4, 7, 9, 10</span>].</p><p>Multisystem involvement makes long COVID-19 management challenging. To date, only cognitive and exercise training interventions alone or combined have shown promise of improvement in cognitive, pulmonary and physical function over usual care; a plethora of other interventions, including drugs, food supplementation and neurological approaches, did not provide benefits (Figure 1) [<span>11, 12</span>]. With pulmonary symptoms at a centre stage, several exercise training modalities for patients with long-COVID were effectively translated from standard pulmonary rehabilitation [<span>13</span>], while the inspiratory muscle training alone demonstrated no added benefit. Therefore, the search for safe and effective pulmonary or systemic intervention that would additionally restore pulmonary function continues.</p><p>Over the recent years, the manipulations of ambient oxygen (O<sub>2</sub>) (e.g., hypoxic and hyperoxic conditioning) have emerged as a therapeutic strategy from sports performance settings, which lead to development of different hypoxic interventions, including intermittent hypoxia conditioning (IHC; e.g., short daily repeated bouts of breathing moderate hypoxia [F<sub>IO2</sub> usually 9–15%] interspersed with intervals breathing ambient air) [<span>14-16</span>]. The application of IHC can provoke improvements in many physiological and functional systems (e.g., cardiopulmonary function, exercise performance, glucose metabolism and weight management) in both athletes and chronic disease patients [<span>14-18</span>]. In patients with cardiovascular disease, resting IHC reduced resting heart rate, systolic and diastolic blood pressure [<span>17</span>]. In addition, early studies from the Soviet Union also suggested potential improvements in myocardial function, blood pressure and sympathetic nervous system regulation [<span>16</span>].</p><p>As previous clinical studies in cardiometabolic patients [<span>14, 16-18</span>] suggested benefits of IHC for use in rehabilitation of patients with long COVID-19, Doehner et al. sought to determine whether such benefits can be translated to rehabilitation of patients with long COVID-19 in a pilot trial recently published in the <i>Journal</i> [<span>19</span>]. The study included 145 overweight, middle-aged patients with long COVID-19 and coexisting arterial hypertension that were allocated to 5 weeks of either combination of IHC with extensive, multidisciplinary rehabilitation program (IHC + rehab, <i>n</i> = 70) or to extensive, multidisciplinary rehabilitation programme alone (rehab, <i>n</i> = 75). The IHC intervention was performed in three weekly sessions consisting of rather standardised six to eight intervals of 3–5 min of breathing a hypoxic air mixture (10%–12% of O<sub>2</sub>) interspersed with 3–5 min of breathing a slightly hyperoxic air mixture (30%–35% of O<sub>2</sub>). After 45 min of IHC, patients continued with multimodal rehabilitation consisting of <i>physical therapy</i> (inspiratory muscle training, electrotherapy, hydrotherapy, etc), <i>exercise training</i> (progressive aerobic, resistance, balance and coordination training), <i>occupational training</i> (cognitive and motor training for improving activities of daily life) and <i>interdisciplinary educational counselling</i> with <i>psychosocial support</i> focused on improving self-management of long COVID-19 disease [<span>19</span>]. The primary study outcome was the change in (sub)maximal endurance (6-min walk test distance) along with integrative assessment of strength (hand grip strength, nine-hole peg test, timed up-and-go test and functional ambulatory capacity), pulmonary capacity, symptoms of dyspnoea, health-related quality of life, blood pressure and biomarkers of inflammation, glucose metabolism and kidney function [<span>19</span>]. The combination of IHC and multidisciplinary rehabilitation appeared safe, well-tolerated and showed a superior effect on improving 6 -min walk test distance (+59 m), stair climbing time (−1.4 s), health-related quality of life (European Quality of Life Five Dimensions Questionnaire analogue scale: +28.4 points) and on long COVID-19 symptoms (Median COVID-19 Recovery Score: −10.2 points) compared with multidisciplinary rehabilitation alone.</p><p>While Doehner et al. [<span>19</span>] should be applauded for taking the first step in exploring the potential of IHC as added tool to standard, mainly exercise-based rehabilitation of patients with long COVID-19, there remain some important considerations for advancing our understanding and applicability of this approach. First, the study findings should be tested in future well-powered randomised, controlled trials, with special emphasis on the appropriate group allocation, which represents one of the limitations in the present study and might partially underscored primary outcome (6-min walk test). Future work should also aim to balance biological sex in the sample, as the present study enrolled mostly female patients likely due to higher prevalence of the syndrome compared to males [<span>2, 3, 19</span>]. Second, future studies should put special emphasis on improving prescription and progression of exercise training, particularly resistance training [<span>20, 21</span>], to counterbalance the cardiopulmonary and skeletal muscle impairments associated with long COVID-19 sequalae [<span>7</span>], which may accelerate sarcopenia in these patient group [<span>2, 6</span>]. Optimised resistance training should be complemented with the inclusion of advanced measurement of body composition (e.g., dual-energy X-ray absorptiometry) and skeletal muscle histology and metabolism (e.g., biopsies on <i>m. vastus lateralis</i>) to gain novel insights into the changes of muscle quality and quantity (Figure 1). Nevertheless, Doehner et al. [<span>19</span>] provide a strong foundation to optimise future exercise training interventions, as solely multidisciplinary rehabilitation approach demonstrated clinical meaningful improvements in 6-min walk test. Thirdly, the benefits of current somewhat standardised IHC protocol combined with pulmonary rehabilitation [<span>13</span>] can be enhanced with further IHC protocol adjustments (changes in hypoxia/hyperoxia ratio, extended exposure per set and within single session) [<span>14</span>], especially for long COVID-19 patient with severe exercise participation-limiting symptoms. Lastly, the benefits of combined IHC with standard pulmonary rehabilitation [<span>13</span>] should be tested in a longer intervention (8–12 weeks) with extended follow-up (≥ 1 year), to investigate whether IHC effects are maintained over longer period of time or whether long COVID-19 symptoms can present again [<span>2</span>].</p><p>The application of IHC, as suggested by Doehner et al. [<span>19</span>], should undoubtedly be considered in rehabilitation of patients with long COVID-19 syndrome and can be effectively combined within the current scheme of standard pulmonary rehabilitation [<span>13</span>]. After extensive clinical assessment [<span>13, 19</span>], the IHC can be introduced in the early phases of long COVID-19 rehabilitation, preferably immediately after COVID-19 infection hospitalisation for patients with severe symptoms of breathlessness and exercise intolerance. Therefore, in early phases of rehabilitation (1–4 weeks), IHC can be added to inspiratory muscle training, low-to-moderate intensity continuous aerobic training (40%–60% of peak O<sub>2</sub> consumption, 45–60 min) and resistance training (3–5 sets of 15–20 repetitions at 40%–60% of maximal muscle strength), balance training and other cognitive and physical therapy interventions [<span>11, 13</span>]. In the later phases of long COVID-19 rehabilitation (5–12 weeks), the intensity of exercise training can be progressively increased (aerobic training: 60%–80% of peak O<sub>2</sub> consumption; resistance training: 70%–80% of muscle strength) [<span>13, 21</span>], while the use of IHC and balance training should be predominantly applied for patients with persistent moderate-to-severe symptoms of breathlessness, exercise intolerance and dizziness and vertigo, respectively. Such individualised approach may further optimise the intensive multidisciplinary rehabilitation of long COVID-19 and consequently help reduce the long-term burden of the syndrome [<span>2, 3, 10, 21</span>].</p><p>In summary, the future of multimodal long COVID-19 rehabilitation consisting of concurrent exercise training [<span>21</span>] and behavioural interventions [<span>11</span>] combined with effective IHC looks bright. Prospective work is nevertheless, warranted, to provide further insights into the question whether the short-term effects of IHC timely presented by Doehner et al. [<span>19</span>] can be maintained/enhanced by using a longer, individually tailored interventions for the most vulnerable patients' populations with persistent long COVID-19 syndromes (patients with pre-existing sarcopenia, after longer hospitalisation and/or with multiple metabolic and cardiopulmonary comorbidities).</p><p>The authors declare no conflicts of interest.</p>","PeriodicalId":48911,"journal":{"name":"Journal of Cachexia Sarcopenia and Muscle","volume":"16 2","pages":""},"PeriodicalIF":9.4000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jcsm.13769","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cachexia Sarcopenia and Muscle","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jcsm.13769","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Since the outbreak of the Coronavirus-19 (COVID-19) pandemic in December 2019, nearly 705 million people got infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and more than 7 million people died [1]. Following recovery from acute COVID-19 infection, many individuals continue to suffer from long-term sequelae of SARS-CoV-2 infection (≥ 3 months) defined as long COVID-19 syndrome or post COVID condition [2-4]. Unsurprisingly, incidence of long COVID-19 syndrome is the highest among hospitalised unvaccinated individuals (50%–85%) and the lowest among vaccinated people (8–12%) and in most cases persisted more than 1 year [2]. The greater risk and most severe symptoms of long COVID-19 were manifested in females aged 35–50 years, patients with comorbidities (type 2 diabetes, allergies, lung diseases, heart failure, chronic kidney disease and obesity) and in unvaccinated individuals [2-5]. Sarcopenia is highly prevalent in patients with long COVID-19, particularly after longer hospitalisation [6].

Long COVID-19 is a heterogeneous, systemic and multiorgan syndrome that has been associated with > 200 different symptoms. The accumulation of SARS-CoV-2 in the tissues, dysregulated immune response, inflammation and endothelial dysfunction induce damage to pulmonary (lung fibrosis and alveolar epithelium injury), cardiovascular (peri-myocarditis, arterial inflammation, micro-thrombosis and coagulopathy), skeletal muscle (muscle fibre atrophy and disrupted mitochondrial function) [7, 8], neurological (postural orthostatic tachycardia and dysautonomia) and autoimmune (onset of autoimmune diseases) systems (Figure 1) [2-4, 9]. These impairments are primarily manifested as fatigue, cough, shortness of breath at rest and after exercise, exercise intolerance, chest pain, joint and muscle pain, cognitive impairments (dizziness, brain fog) and sleep disorders, along with other less frequent symptoms [2-4, 7, 9, 10].

Multisystem involvement makes long COVID-19 management challenging. To date, only cognitive and exercise training interventions alone or combined have shown promise of improvement in cognitive, pulmonary and physical function over usual care; a plethora of other interventions, including drugs, food supplementation and neurological approaches, did not provide benefits (Figure 1) [11, 12]. With pulmonary symptoms at a centre stage, several exercise training modalities for patients with long-COVID were effectively translated from standard pulmonary rehabilitation [13], while the inspiratory muscle training alone demonstrated no added benefit. Therefore, the search for safe and effective pulmonary or systemic intervention that would additionally restore pulmonary function continues.

Over the recent years, the manipulations of ambient oxygen (O2) (e.g., hypoxic and hyperoxic conditioning) have emerged as a therapeutic strategy from sports performance settings, which lead to development of different hypoxic interventions, including intermittent hypoxia conditioning (IHC; e.g., short daily repeated bouts of breathing moderate hypoxia [FIO2 usually 9–15%] interspersed with intervals breathing ambient air) [14-16]. The application of IHC can provoke improvements in many physiological and functional systems (e.g., cardiopulmonary function, exercise performance, glucose metabolism and weight management) in both athletes and chronic disease patients [14-18]. In patients with cardiovascular disease, resting IHC reduced resting heart rate, systolic and diastolic blood pressure [17]. In addition, early studies from the Soviet Union also suggested potential improvements in myocardial function, blood pressure and sympathetic nervous system regulation [16].

As previous clinical studies in cardiometabolic patients [14, 16-18] suggested benefits of IHC for use in rehabilitation of patients with long COVID-19, Doehner et al. sought to determine whether such benefits can be translated to rehabilitation of patients with long COVID-19 in a pilot trial recently published in the Journal [19]. The study included 145 overweight, middle-aged patients with long COVID-19 and coexisting arterial hypertension that were allocated to 5 weeks of either combination of IHC with extensive, multidisciplinary rehabilitation program (IHC + rehab, n = 70) or to extensive, multidisciplinary rehabilitation programme alone (rehab, n = 75). The IHC intervention was performed in three weekly sessions consisting of rather standardised six to eight intervals of 3–5 min of breathing a hypoxic air mixture (10%–12% of O2) interspersed with 3–5 min of breathing a slightly hyperoxic air mixture (30%–35% of O2). After 45 min of IHC, patients continued with multimodal rehabilitation consisting of physical therapy (inspiratory muscle training, electrotherapy, hydrotherapy, etc), exercise training (progressive aerobic, resistance, balance and coordination training), occupational training (cognitive and motor training for improving activities of daily life) and interdisciplinary educational counselling with psychosocial support focused on improving self-management of long COVID-19 disease [19]. The primary study outcome was the change in (sub)maximal endurance (6-min walk test distance) along with integrative assessment of strength (hand grip strength, nine-hole peg test, timed up-and-go test and functional ambulatory capacity), pulmonary capacity, symptoms of dyspnoea, health-related quality of life, blood pressure and biomarkers of inflammation, glucose metabolism and kidney function [19]. The combination of IHC and multidisciplinary rehabilitation appeared safe, well-tolerated and showed a superior effect on improving 6 -min walk test distance (+59 m), stair climbing time (−1.4 s), health-related quality of life (European Quality of Life Five Dimensions Questionnaire analogue scale: +28.4 points) and on long COVID-19 symptoms (Median COVID-19 Recovery Score: −10.2 points) compared with multidisciplinary rehabilitation alone.

While Doehner et al. [19] should be applauded for taking the first step in exploring the potential of IHC as added tool to standard, mainly exercise-based rehabilitation of patients with long COVID-19, there remain some important considerations for advancing our understanding and applicability of this approach. First, the study findings should be tested in future well-powered randomised, controlled trials, with special emphasis on the appropriate group allocation, which represents one of the limitations in the present study and might partially underscored primary outcome (6-min walk test). Future work should also aim to balance biological sex in the sample, as the present study enrolled mostly female patients likely due to higher prevalence of the syndrome compared to males [2, 3, 19]. Second, future studies should put special emphasis on improving prescription and progression of exercise training, particularly resistance training [20, 21], to counterbalance the cardiopulmonary and skeletal muscle impairments associated with long COVID-19 sequalae [7], which may accelerate sarcopenia in these patient group [2, 6]. Optimised resistance training should be complemented with the inclusion of advanced measurement of body composition (e.g., dual-energy X-ray absorptiometry) and skeletal muscle histology and metabolism (e.g., biopsies on m. vastus lateralis) to gain novel insights into the changes of muscle quality and quantity (Figure 1). Nevertheless, Doehner et al. [19] provide a strong foundation to optimise future exercise training interventions, as solely multidisciplinary rehabilitation approach demonstrated clinical meaningful improvements in 6-min walk test. Thirdly, the benefits of current somewhat standardised IHC protocol combined with pulmonary rehabilitation [13] can be enhanced with further IHC protocol adjustments (changes in hypoxia/hyperoxia ratio, extended exposure per set and within single session) [14], especially for long COVID-19 patient with severe exercise participation-limiting symptoms. Lastly, the benefits of combined IHC with standard pulmonary rehabilitation [13] should be tested in a longer intervention (8–12 weeks) with extended follow-up (≥ 1 year), to investigate whether IHC effects are maintained over longer period of time or whether long COVID-19 symptoms can present again [2].

The application of IHC, as suggested by Doehner et al. [19], should undoubtedly be considered in rehabilitation of patients with long COVID-19 syndrome and can be effectively combined within the current scheme of standard pulmonary rehabilitation [13]. After extensive clinical assessment [13, 19], the IHC can be introduced in the early phases of long COVID-19 rehabilitation, preferably immediately after COVID-19 infection hospitalisation for patients with severe symptoms of breathlessness and exercise intolerance. Therefore, in early phases of rehabilitation (1–4 weeks), IHC can be added to inspiratory muscle training, low-to-moderate intensity continuous aerobic training (40%–60% of peak O2 consumption, 45–60 min) and resistance training (3–5 sets of 15–20 repetitions at 40%–60% of maximal muscle strength), balance training and other cognitive and physical therapy interventions [11, 13]. In the later phases of long COVID-19 rehabilitation (5–12 weeks), the intensity of exercise training can be progressively increased (aerobic training: 60%–80% of peak O2 consumption; resistance training: 70%–80% of muscle strength) [13, 21], while the use of IHC and balance training should be predominantly applied for patients with persistent moderate-to-severe symptoms of breathlessness, exercise intolerance and dizziness and vertigo, respectively. Such individualised approach may further optimise the intensive multidisciplinary rehabilitation of long COVID-19 and consequently help reduce the long-term burden of the syndrome [2, 3, 10, 21].

In summary, the future of multimodal long COVID-19 rehabilitation consisting of concurrent exercise training [21] and behavioural interventions [11] combined with effective IHC looks bright. Prospective work is nevertheless, warranted, to provide further insights into the question whether the short-term effects of IHC timely presented by Doehner et al. [19] can be maintained/enhanced by using a longer, individually tailored interventions for the most vulnerable patients' populations with persistent long COVID-19 syndromes (patients with pre-existing sarcopenia, after longer hospitalisation and/or with multiple metabolic and cardiopulmonary comorbidities).

The authors declare no conflicts of interest.

Abstract Image

间歇性缺氧训练能否增强标准长 COVID-19 康复训练的益处?
自2019年12月冠状病毒-19 (COVID-19)大流行爆发以来,近7.05亿人感染了严重急性呼吸综合征冠状病毒2 (SARS-CoV-2), 700多万人死亡。在急性COVID-19感染康复后,许多个体继续遭受SARS-CoV-2感染的长期后遗症(≥3个月),定义为长期COVID-19综合征或COVID后状态[2-4]。不出所料,长期COVID-19综合征的发病率在未接种疫苗的住院患者中最高(50%-85%),在接种疫苗的人群中最低(8-12%),并且在大多数情况下持续1年以上。35-50岁的女性、有合并症(2型糖尿病、过敏、肺部疾病、心力衰竭、慢性肾脏疾病和肥胖)的患者和未接种疫苗的个体表现出更大的风险和最严重的症状[2-5]。肌肉减少症在长期感染COVID-19的患者中非常普遍,特别是在住院时间较长的患者中。长期以来,COVID-19是一种异质性、全身性和多器官综合征,与200种不同症状有关。SARS-CoV-2在组织中的积累、免疫反应失调、炎症和内皮功能障碍导致肺(肺纤维化和肺泡上皮损伤)、心血管(心肌炎、动脉炎症、微血栓形成和凝血功能障碍)、骨骼肌(肌纤维萎缩和线粒体功能中断)的损伤[7,8]。神经系统(体位性心动过速和自主神经异常)和自身免疫系统(自身免疫性疾病的发病)(图1)[2- 4,9]。这些损害主要表现为疲劳、咳嗽、休息时和运动后呼吸短促、运动不耐受、胸痛、关节和肌肉疼痛、认知障碍(头晕、脑雾)和睡眠障碍,以及其他不常见的症状[2- 4,7,9,10]。多系统参与使得COVID-19的长期管理具有挑战性。迄今为止,只有认知和运动训练干预单独或联合显示出比常规护理更有希望改善认知、肺和身体功能;过多的其他干预措施,包括药物、食物补充和神经方法,都没有提供益处(图1)[11,12]。在肺部症状处于中心阶段的情况下,长期covid患者的几种运动训练方式可以有效地从标准肺部康复[13]转化为标准,而单独的吸气肌训练没有显示出额外的益处。因此,继续寻找安全有效的肺部或全身干预措施,以进一步恢复肺功能。近年来,环境氧(O2)的操作(例如,低氧和高氧条件)已经成为运动表现设置的一种治疗策略,这导致了不同的低氧干预措施的发展,包括间歇性低氧条件(IHC;例如,每天短时间反复呼吸中度缺氧[FIO2通常为9-15%],间隔期呼吸环境空气)[14-16]。IHC的应用可以改善运动员和慢性疾病患者的许多生理和功能系统(如心肺功能、运动表现、葡萄糖代谢和体重管理)[14-18]。在心血管疾病患者中,静息IHC可降低静息心率、收缩压和舒张压。此外,来自苏联的早期研究也表明心肌功能,血压和交感神经系统调节[16]的潜在改善。由于先前在心脏代谢患者中的临床研究[14,16-18]表明IHC用于长链COVID-19患者康复的益处,Doehner等人在最近发表在bbb杂志上的一项试点试验中试图确定这种益处是否可以转化为长链COVID-19患者的康复。该研究包括145名超重、长期患有COVID-19并并存动脉高血压的中年患者,他们被分配到5周的免疫结合广泛的多学科康复计划(免疫结合+康复,n = 70)或广泛的多学科康复计划单独(康复,n = 75)。IHC干预每周进行3次,包括相当标准化的6至8次间隔,每次呼吸3-5分钟的低氧空气混合物(10%-12%的O2),穿插3-5分钟的轻度高氧空气混合物(30%-35%的O2)。 45分钟IHC后,患者继续接受多模式康复治疗,包括物理治疗(吸气肌训练、电疗、水疗等)、运动训练(渐进式有氧、阻力、平衡和协调训练)、职业训练(改善日常生活活动的认知和运动训练)以及跨学科教育咨询和社会心理支持,重点是改善COVID-19长期疾病[19]的自我管理。主要研究结果是(亚)最大耐力(6分钟步行测试距离)的变化,以及力量综合评估(握力、九孔钉测试、定时起跑测试和功能性移动能力)、肺活量、呼吸困难症状、健康相关生活质量、血压和炎症生物标志物、葡萄糖代谢和肾功能[19]。IHC联合多学科康复治疗安全、耐受性良好,与单独多学科康复治疗相比,在改善6分钟步行测试距离(+59 m)、爬楼梯时间(- 1.4 s)、健康相关生活质量(欧洲生活质量五维度问卷模拟量表:+28.4分)和长期COVID-19症状(中位COVID-19恢复评分:- 10.2分)方面均有显著效果。虽然Doehner等人在探索IHC作为标准工具(主要是长期COVID-19患者的基于运动的康复)的潜力方面迈出了第一步,应该受到赞扬,但在提高我们对这种方法的理解和适用性方面仍有一些重要的考虑。首先,研究结果应在未来的有力随机对照试验中进行检验,特别强调适当的组分配,这是本研究的局限性之一,可能部分强调主要结果(6分钟步行试验)。未来的工作还应致力于平衡样本中的生理性别,因为本研究主要招募了女性患者,可能是因为该综合征的患病率高于男性[2,3,19]。其次,未来的研究应特别重视改善运动训练的处方和进展,特别是阻力训练[20,21],以平衡与COVID-19长期后遗症[7]相关的心肺和骨骼肌损伤,这些损伤可能加速这些患者组的肌肉减少[2,6]。优化的抗阻训练应与先进的身体成分测量(如双能x线吸收仪)、骨骼肌组织学和代谢(如股外侧肌活检)相结合,以获得对肌肉质量和数量变化的新见解(图1)。尽管如此,Doehner等人[bbb]为优化未来的运动训练干预提供了坚实的基础。作为唯一的多学科康复方法在6分钟步行试验中表现出临床意义的改善。第三,通过进一步调整IHC方案(低氧/高氧比例的变化、每次和单次暴露时间的延长)[14],特别是对于长期存在严重运动参与限制症状的COVID-19患者,目前某种程度上标准化的IHC方案结合肺康复[13]的益处可以得到增强。最后,应在更长时间的干预(8-12周)和延长随访(≥1年)中测试IHC联合标准肺康复[2]的益处,以调查IHC的效果是否能在更长的时间内维持,或者长时间的COVID-19症状是否会再次出现[2]。Doehner等人[19]建议的IHC应用在COVID-19长期综合征患者的康复中无疑是应该考虑的,并且可以在现行标准肺康复[13]方案中有效结合。经过广泛的临床评估[13,19],IHC可在COVID-19长期康复的早期阶段引入,最好是在COVID-19感染住院后立即引入,患者有严重的呼吸困难和运动不耐受症状。因此,在康复早期(1-4周),IHC可加入吸气肌训练、中低强度连续有氧训练(峰值耗氧量的40%-60%,45-60分钟)和阻力训练(3-5组,每次15-20次,最大肌力的40%-60%)、平衡训练等认知和物理治疗干预[11,13]。 在COVID-19长期康复的后期(5-12周),可以逐步增加运动训练的强度(有氧训练:峰值耗氧量的60%-80%;阻力训练:肌力的70%-80%)[13,21],而对于持续出现中重度呼吸困难、运动不耐受和头晕眩晕症状的患者,应主要采用IHC和平衡训练。这种个性化的方法可以进一步优化长期COVID-19的密集多学科康复,从而有助于减轻该综合征的长期负担[2,3,10,21]。综上所述,由并行运动训练[21]和行为干预[11]结合有效免疫结构组成的多模式COVID-19长期康复的未来前景光明。然而,有必要开展前瞻性工作,以进一步了解Doehner等人及时提出的IHC的短期效果是否可以通过对持续长期COVID-19综合征的最脆弱患者群体(患有先前存在的肌肉减少症,住院时间较长和/或患有多种代谢和心肺合并症的患者)使用更长时间的量身定制干预措施来维持/增强。作者声明无利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Cachexia Sarcopenia and Muscle
Journal of Cachexia Sarcopenia and Muscle MEDICINE, GENERAL & INTERNAL-
CiteScore
13.30
自引率
12.40%
发文量
234
审稿时长
16 weeks
期刊介绍: The Journal of Cachexia, Sarcopenia and Muscle is a peer-reviewed international journal dedicated to publishing materials related to cachexia and sarcopenia, as well as body composition and its physiological and pathophysiological changes across the lifespan and in response to various illnesses from all fields of life sciences. The journal aims to provide a reliable resource for professionals interested in related research or involved in the clinical care of affected patients, such as those suffering from AIDS, cancer, chronic heart failure, chronic lung disease, liver cirrhosis, chronic kidney failure, rheumatoid arthritis, or sepsis.
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