恶病质管理的多模式干预。

IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Joanne Reid, Carolyn Blair, Martin Dempster, Clare McKeaveney, Adrian Slee, Donna Fitzsimons
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Multimodal interventions which work synergistically to treat the syndrome could lead to benefits.</p><p><strong>Objectives: </strong>To assess the benefits and harms of multimodal interventions aimed at alleviating or stabilising cachexia in people with a chronic illness.</p><p><strong>Search methods: </strong>We searched CENTRAL, MEDLINE, Embase, PsycINFO, and two trials registers in July 2024, together with reference checking, citation searching, and contact with study authors to identify studies.</p><p><strong>Selection criteria: </strong>We included randomised controlled trials (RCTs) in adults with or at risk of cachexia, comparing multimodal interventions combining two or more modalities (of pharmacology, nutrition, exercise) to treatment as usual, variation of the intervention, or unimodal intervention.</p><p><strong>Data collection and analysis: </strong>Two review authors independently screened potentially eligible studies, extracted data, and assessed risk of bias (RoB 1). Primary outcomes were physical function, strength, and adverse events. Secondary outcomes were body composition and weight, quality of life (QoL), appetite, fatigue, and biochemical markers. We assessed the certainty of evidence with GRADE.</p><p><strong>Main results: </strong>We included nine studies with 926 adults (mean age: 63 years). Study sample sizes ranged from 20 to 332 participants. Six studies were conducted in Europe, and one each in Turkey, New Zealand, and the USA. There were six studies in people with cancer, and one each in people with COPD, chronic kidney disease, and HIV/AIDS. We judged four studies to be at an overall high risk of bias, and five at an overall unclear risk. All outcomes in all comparisons had very low-certainty evidence, downgraded once for risk of bias and/or indirectness and twice for imprecision. Multimodal intervention (pharmacological, nutritional, and/or exercise) compared to treatment as usual One cancer study randomised 46 participants, with 41 included in all analyses except adverse events. The study assessed outcomes immediately after treatment, lasting six weeks. Compared to treatment as usual, there is no clear evidence for an effect of a multimodal intervention on: physical function (mean difference (MD) -16.10 m, 95% confidence interval (CI) -79.06 to 46.86; 41 participants); strength (MD 3.80 kg, 95% CI -3.21 to 10.81; 41 participants); adverse events (risk ratio (RR) 1.36, 95% CI 0.70 to 2.65; 46 participants); body composition (MD 7.89 cm<sup>2</sup>, 95% CI -10.43 to 26.21; 41 participants); weight (MD 5.89 kg, 95% CI -1.45 to 13.23; 41 participants); appetite (MD 0.68 points, 95% CI -0.60 to 1.96; 41 participants); fatigue (MD 0.12, 95% CI -1.05 to 1.29; 41 participants); and biochemical markers (MD 2%, 95% CI 0.99 to 3.01; 41 participants), but the evidence was very uncertain; QoL was not reported. Multimodal intervention compared to variation of the intervention Three cancer studies and one HIV/AIDS study randomised 192 participants. We could not use the available data, nor obtain additional data, from two studies (one in cancer, one in HIV/AIDS). The studies assessed outcomes immediately after treatment, ranging from three to seven months. Compared to a variation of the intervention, there is no clear evidence for an effect of a multimodal intervention on: physical function (MD 10.0 m, 95% CI -36.27 to 56.27; 1 study, 56 participants); strength (MD 0.7 kg, 95% CI -3.75 to 5.15; 1 study, 56 participants); adverse events (RR 0.87, 95% CI 0.38 to 2.02; P = 0.75, I<sup>2</sup> = 0%; 2 studies, 95 participants); body composition (MD -2.67 kg, 95% CI -5.89 to 0.54; P = 0.10, I<sup>2</sup> = 0%; 2 studies, 95 participants); weight (MD -2.47 kg, 95% CI -7.11 to 2.16; P = 0.30, I<sup>2</sup> = 0%; 2 studies, 95 participants); QoL (standardised mean difference (SMD) -0.15, 95% CI -0.55 to 0.26; P = 0.47, I<sup>2</sup> = 0%; 2 studies, 95 participants); appetite (SMD -0.34, 95% CI -1.27 to 0.59; P = 0.48, I<sup>2</sup> = 79%; 2 studies, 95 participants); fatigue (MD 6.40 points, 95% CI -1.10 to 13.90; 1 study, 56 participants); or biochemical markers (MD 9.80 pg/mL, 95% CI -6.25 to 25.85; P = 0.23, I<sup>2</sup> = 73%; 2 studies, 95 participants), but the evidence is very uncertain. Multimodal intervention compared to unimodal intervention We included six studies (802 participants) in this comparison: three cancer studies, and one each in people with COPD, chronic kidney disease, and HIV/AIDS. The studies assessed outcomes immediately after treatment, ranging from three to seven months. We could not use the available data, nor obtain additional data, from the HIV/AIDS study. 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The certainty of the evidence was very low. 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Multimodal intervention (pharmacological, nutritional, and/or exercise) compared to treatment as usual One cancer study randomised 46 participants, with 41 included in all analyses except adverse events. The study assessed outcomes immediately after treatment, lasting six weeks. Compared to treatment as usual, there is no clear evidence for an effect of a multimodal intervention on: physical function (mean difference (MD) -16.10 m, 95% confidence interval (CI) -79.06 to 46.86; 41 participants); strength (MD 3.80 kg, 95% CI -3.21 to 10.81; 41 participants); adverse events (risk ratio (RR) 1.36, 95% CI 0.70 to 2.65; 46 participants); body composition (MD 7.89 cm<sup>2</sup>, 95% CI -10.43 to 26.21; 41 participants); weight (MD 5.89 kg, 95% CI -1.45 to 13.23; 41 participants); appetite (MD 0.68 points, 95% CI -0.60 to 1.96; 41 participants); fatigue (MD 0.12, 95% CI -1.05 to 1.29; 41 participants); and biochemical markers (MD 2%, 95% CI 0.99 to 3.01; 41 participants), but the evidence was very uncertain; QoL was not reported. Multimodal intervention compared to variation of the intervention Three cancer studies and one HIV/AIDS study randomised 192 participants. 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引用次数: 0

摘要

02, 95% CI -0.22 ~ 0.26;P = 0.86, i2 = 0%;2项研究,348名受试者);强度(SMD = 0.23, 95% CI = -0.81 ~ 1.27;P = 0.66, i2 = 0%;2项研究,348名受试者);不良事件(RR 0.87, 95% CI -0.43 ~ 1.73;P = 0.68, i2 = 45%;2项研究,395名受试者);体成分(SMD = 0.11, 95% CI = -0.28 ~ 0.50;P = 0.58, i2 = 74%;5项研究,742名受试者);体重(SMD -0.02, 95% CI -0.38 ~ 0.33;P = 0.90, i2 = 49%;4项研究,431名参与者);生活质量(SMD = 0.22, 95% CI = -0.29 ~ 0.73;P = 0.39, i2 = 61%;3项研究,411名参与者);食欲(SMD -0.09, 95% CI -0.58 ~ 0.40;P = 0.72, i2 = 58%;2项研究,395名受试者);疲劳(MD -6.80点,95% CI -12.44 ~ -1.17;1项研究,244名参与者);生化指标(SMD = 0.11, 95% CI = -0.59 ~ 0.80;P = 0.76, i2 = 79%;3项研究,411名参与者),但证据非常不确定。作者的结论:该综述没有发现足够的证据来支持或反驳在管理恶病质中使用多模式干预措施。证据的确定性很低。评估多模式干预在慢性疾病中管理恶病质的有效性,需要方法学严谨、动力充足、相互作用时间充足的随机对照试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal interventions for cachexia management.

Background: Cachexia (disease-related wasting) is a complex metabolic syndrome which occurs in people with chronic illnesses, including cancer, HIV/AIDS, kidney disease, heart disease, and chronic obstructive pulmonary disease (COPD). People with cachexia experience unintentional weight loss, muscle loss, fatigue, loss of appetite, and reduced quality of life. Multimodal interventions which work synergistically to treat the syndrome could lead to benefits.

Objectives: To assess the benefits and harms of multimodal interventions aimed at alleviating or stabilising cachexia in people with a chronic illness.

Search methods: We searched CENTRAL, MEDLINE, Embase, PsycINFO, and two trials registers in July 2024, together with reference checking, citation searching, and contact with study authors to identify studies.

Selection criteria: We included randomised controlled trials (RCTs) in adults with or at risk of cachexia, comparing multimodal interventions combining two or more modalities (of pharmacology, nutrition, exercise) to treatment as usual, variation of the intervention, or unimodal intervention.

Data collection and analysis: Two review authors independently screened potentially eligible studies, extracted data, and assessed risk of bias (RoB 1). Primary outcomes were physical function, strength, and adverse events. Secondary outcomes were body composition and weight, quality of life (QoL), appetite, fatigue, and biochemical markers. We assessed the certainty of evidence with GRADE.

Main results: We included nine studies with 926 adults (mean age: 63 years). Study sample sizes ranged from 20 to 332 participants. Six studies were conducted in Europe, and one each in Turkey, New Zealand, and the USA. There were six studies in people with cancer, and one each in people with COPD, chronic kidney disease, and HIV/AIDS. We judged four studies to be at an overall high risk of bias, and five at an overall unclear risk. All outcomes in all comparisons had very low-certainty evidence, downgraded once for risk of bias and/or indirectness and twice for imprecision. Multimodal intervention (pharmacological, nutritional, and/or exercise) compared to treatment as usual One cancer study randomised 46 participants, with 41 included in all analyses except adverse events. The study assessed outcomes immediately after treatment, lasting six weeks. Compared to treatment as usual, there is no clear evidence for an effect of a multimodal intervention on: physical function (mean difference (MD) -16.10 m, 95% confidence interval (CI) -79.06 to 46.86; 41 participants); strength (MD 3.80 kg, 95% CI -3.21 to 10.81; 41 participants); adverse events (risk ratio (RR) 1.36, 95% CI 0.70 to 2.65; 46 participants); body composition (MD 7.89 cm2, 95% CI -10.43 to 26.21; 41 participants); weight (MD 5.89 kg, 95% CI -1.45 to 13.23; 41 participants); appetite (MD 0.68 points, 95% CI -0.60 to 1.96; 41 participants); fatigue (MD 0.12, 95% CI -1.05 to 1.29; 41 participants); and biochemical markers (MD 2%, 95% CI 0.99 to 3.01; 41 participants), but the evidence was very uncertain; QoL was not reported. Multimodal intervention compared to variation of the intervention Three cancer studies and one HIV/AIDS study randomised 192 participants. We could not use the available data, nor obtain additional data, from two studies (one in cancer, one in HIV/AIDS). The studies assessed outcomes immediately after treatment, ranging from three to seven months. Compared to a variation of the intervention, there is no clear evidence for an effect of a multimodal intervention on: physical function (MD 10.0 m, 95% CI -36.27 to 56.27; 1 study, 56 participants); strength (MD 0.7 kg, 95% CI -3.75 to 5.15; 1 study, 56 participants); adverse events (RR 0.87, 95% CI 0.38 to 2.02; P = 0.75, I2 = 0%; 2 studies, 95 participants); body composition (MD -2.67 kg, 95% CI -5.89 to 0.54; P = 0.10, I2 = 0%; 2 studies, 95 participants); weight (MD -2.47 kg, 95% CI -7.11 to 2.16; P = 0.30, I2 = 0%; 2 studies, 95 participants); QoL (standardised mean difference (SMD) -0.15, 95% CI -0.55 to 0.26; P = 0.47, I2 = 0%; 2 studies, 95 participants); appetite (SMD -0.34, 95% CI -1.27 to 0.59; P = 0.48, I2 = 79%; 2 studies, 95 participants); fatigue (MD 6.40 points, 95% CI -1.10 to 13.90; 1 study, 56 participants); or biochemical markers (MD 9.80 pg/mL, 95% CI -6.25 to 25.85; P = 0.23, I2 = 73%; 2 studies, 95 participants), but the evidence is very uncertain. Multimodal intervention compared to unimodal intervention We included six studies (802 participants) in this comparison: three cancer studies, and one each in people with COPD, chronic kidney disease, and HIV/AIDS. The studies assessed outcomes immediately after treatment, ranging from three to seven months. We could not use the available data, nor obtain additional data, from the HIV/AIDS study. Compared to a unimodal intervention, there is no clear evidence for an effect of a multimodal intervention on: physical function (SMD 0.02, 95% CI -0.22 to 0.26; P = 0.86, I2 = 0%; 2 studies, 348 participants); strength (SMD 0.23, 95% CI -0.81 to 1.27; P = 0.66, I2 = 0%; 2 studies, 348 participants); adverse events (RR 0.87, 95% CI -0.43 to 1.73; P = 0.68, I2 = 45%; 2 studies, 395 participants); body composition (SMD 0.11, 95% CI -0.28 to 0.50; P = 0.58, I2 = 74%; 5 studies, 742 participants); body weight (SMD -0.02, 95% CI -0.38 to 0.33; P = 0.90, I2 = 49%; 4 studies, 431 participants); QoL (SMD 0.22, 95% CI -0.29 to 0.73; P = 0.39, I2 = 61%; 3 studies, 411 participants); appetite (SMD -0.09, 95% CI -0.58 to 0.40; P = 0.72, I2 = 58%; 2 studies, 395 participants); fatigue (MD -6.80 points, 95% CI -12.44 to -1.17; 1 study, 244 participants); and biochemical markers (SMD 0.11, 95% CI -0.59 to 0.80; P = 0.76, I2 = 79%; 3 studies, 411 participants), but the evidence is very uncertain.

Authors' conclusions: The review found insufficient evidence to support or refute the use of multimodal interventions in managing cachexia. The certainty of the evidence was very low. Methodologically rigorous, well-powered RCTs with adequate interaction times are needed to assess the effectiveness of multimodal interventions in managing cachexia across chronic illnesses.

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来源期刊
CiteScore
10.60
自引率
2.40%
发文量
173
审稿时长
1-2 weeks
期刊介绍: The Cochrane Database of Systematic Reviews (CDSR) stands as the premier database for systematic reviews in healthcare. It comprises Cochrane Reviews, along with protocols for these reviews, editorials, and supplements. Owned and operated by Cochrane, a worldwide independent network of healthcare stakeholders, the CDSR (ISSN 1469-493X) encompasses a broad spectrum of health-related topics, including health services.
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