Effects of early exercise training following severe burn injury: a randomized controlled trial

David R. Schieffelers , Tianfeng Ru , Haonan Dai , Ziqing Ye , Eric van Breda , Ulrike Van Daele , Weiguo Xie , Jun Wu

Burns & Trauma ›› 2024, Vol. 12 ›› Issue (1) : tkae005

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Burns & Trauma ›› 2024, Vol. 12 ›› Issue (1) :tkae005 DOI: 10.1093/burnst/tkae005
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Effects of early exercise training following severe burn injury: a randomized controlled trial
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Abstract

Background: Despite being a stable component of burn rehabilitation at later stages of recovery, exercise training is not commonly provided during the acute phase of burns. A lack of evidence surrounding its efficacy and safety in severely burned adults has hampered its implementation in acute burn care. The aim of this study was to investigate the capacity of early exercise training to modulate parameters of postburn muscle wasting and quality of life. Methods: Adults <65 years of age with burns ≥40% total burn surface area (TBSA) were randomly allocated to either receive early exercise (n = 29) in addition to standard care or standard care alone (n = 29). Early exercise involved resistance and aerobic training, which commenced as early as possible and lasted for a duration of 6 to 12 weeks, in line with burn center length of stay. Ultrasound-derived quadriceps muscle layer thickness (QMLT) and rectus femoris cross-sectional area (RF-CSA), lower limb muscle force, Eurocol Quality of Life-5 Dimensions and Burn Specific Health Scale Brief (BSHS-B) were assessed 6 and 12 weeks after baseline. Mixed models were fitted to compare between-group changes over time. Results: A total of 58 adults [42 (95% confidence interval 40–45) years old; 40–94% TBSA range, 86% previously mechanically ventilated] participated in this study. Exercise commenced 7 days [IQR (interquartile range) 5–9] after burn center admission with an attendance rate of 93%. Allocation to the exercise group had a protective effect on the loss of muscle size from baseline to 6 weeks of follow-up (QMLT: β-coefficient: 0.05 cm, p = 0.010; RF-CSA: β-coefficient: 0.05 cm2, p = 0.045), and resulted in an improved recovery from 6 to 12 weeks (QMLT: β-coefficient: 0.04 cm, p = 0.01; RF-CSA: β-coefficient: 0.06 cm2, p < 0.001). Muscle force increased significantly more in the exercise group than in the control group (β-coefficient: 3.102 N, p < 0.001) between 6 and 12 weeks. Besides a marginally significant effect for the BSHS-B domains ‘affect’ and ‘interpersonal relationships’ between 6 and 12 weeks, no benefits were observed in the other assessed quality-of-life measures. No serious adverse events were reported in the exercise group. Conclusions: The results of this study support the use of early exercise training as a feasible and efficacious therapeutic strategy to manage burn-related changes in muscle size and strength in adults with acute severe burn injury.

Keywords

Burns / Exercise / Rehabilitation / Muscle wasting / Cachexia

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David R. Schieffelers, Tianfeng Ru, Haonan Dai, Ziqing Ye, Eric van Breda, Ulrike Van Daele, Weiguo Xie, Jun Wu. Effects of early exercise training following severe burn injury: a randomized controlled trial. Burns & Trauma, 2024, 12 (1) : tkae005 DOI:10.1093/burnst/tkae005

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References

[1]

Gore DC, Chinkes DL, Wolf SE, Sanford AP, Herndon DN, Wolfe RR. Quantification of protein metabolism in vivo for skin, wound, and muscle in severe burn patients. J Parenter Enter Nutr. 2006; 30: 331-8.

[2]

Porter C, Tompkins RG, Finnerty CC, Sidossis LS, Suman OE, Herndon DN. The metabolic stress response to burn trauma: current understanding and therapies. Lancet. 2016; 388: 1417-26.

[3]

Gore DC, Chinkes DL, Hart DW, Wolf SE, Herndon DN, Sanford AP. Hyperglycemia exacerbates muscle protein catabolism in burn-injured patients. Crit Care Med. 2002; 30: 2438-42.

[4]

Clark AT, Song J, Yao X, Carlson D, Huebinger RM, Mei Liu M, et al. Muscle homeostasis is disrupted in burned adults. J Burn Care Res. 2020; 41: 33-40.

[5]

Merritt EK, Cross JM, Bamman MM. Inflammatory and protein metabolism signaling responses in human skeletal muscle after burn injury. J Burn Care Res. 2012; 33: 291-7.

[6]

Ogunbileje JO, Porter C, Herndon DN, Chao T, Abdelrahman DR, Papadimitriou A, et al. Hypermetabolism and hypercatabolism of skeletal muscle accompany mitochondrial stress following severe burn trauma. Am J Physiol-Endocrinol Metab. 2016; 311: E436-48.

[7]

Hermans G, Van Mechelen H, Clerckx B, Vanhullebusch T, Mesotten D, Wilmer A, et al. Acute outcomes and 1-year mortality of intensive care unit-acquired weakness. A cohort study and propensity-matched analysis. Am J Respir Crit Care Med. 2014; 190: 410-20.

[8]

Moisey LL, Mourtzakis M, Cotton BA, Premji T, Heyland DK, Wade CE, et al. Skeletal muscle predicts ventilator-free days, ICU-free days, and mortality in elderly ICU patients. Crit Care. 2013; 17: R206.

[9]

Randall SM, Fear MW, Wood FM, Rea S, Boyd JH, Duke JM. Long-term musculoskeletal morbidity after adult burn injury: a population-based cohort study. BMJ Open. 2015; 5: e009395. https://doi.org/10.1136/bmjopen-2015-009395.

[10]

Omar MTA, Abd El Baky AM, Ebid AA. Lower-limb muscular strength, balance, and mobility levels in adults following severe thermal burn injuries. J Burn Care Res. 2017; 38: 327-33.

[11]

St-Pierre DMM, Choinière M, Forget R, Garrel DR. Muscle strength in individuals with healed burns. Arch Phys Med Rehabil. 1998; 79: 155-61.

[12]

Demling RH. The role of anabolic hormones for wound healing in catabolic states. J Burns Wounds. 2005; 4: e2.

[13]

Argilés JM, Campos N, Lopez-Pedrosa JM, Rueda R, Rodriguez-Mañas L. Skeletal muscle regulates metabolism via interorgan crosstalk: roles in health and disease. J Am Med Dir Assoc. 2016; 17: 789-96.

[14]

Tazerout S, Martinez O, Monsonis B, Millet I, Taourel P, Capdevila X, et al. Acute post-traumatic muscle atrophy on CT scan predicts prolonged mechanical ventilation and a worse outcome in severe trauma patients. Injury. 2022; 53: 2501-10.

[15]

Nakanishi N, Oto J, Tsutsumi R, Akimoto Y, Nakano Y, Nishimura M. Upper limb muscle atrophy associated with in-hospital mortality and physical function impairments in mechanically ventilated critically ill adults: a two-center prospective observational study. J Intensive Care. 2020; 8: 87.

[16]

Tang D, Li-Tsang CWP, Au RKC, Shen X, Li K, Yi X, et al. Predictors of functional independence, quality of life, and return to work in patients with burn injuries in mainland China. Burns Trauma. 2016; 4: s41038, 32-016-0058-4.

[17]

Chung S-D, Chen C-S, Lin H-C, Kang J-H. Increased risk for stroke in burn patients: a population-based one-year follow-up study. Burns. 2014; 40: 54-60.

[18]

Duke JM, Randall SM, Fear MW, Boyd JH, O’Halloran E, Rea S, et al. Increased admissions for diabetes mellitus after burn. Burns. 2016; 42: 1734-9.

[19]

Duke JM, Randall SM, Fear MW, Boyd JH, Rea S, Wood FM. Understanding the long-term impacts of burn on the cardiovascular system. Burns. 2016; 42: 366-74.

[20]

Cree MG, Fram RY, Barr D, Chinkes D, Wolfe RR, Herndon DN. Insulin resistance, secretion and breakdown are increased 9 months following severe burn injury. Burns. 2009; 35: 63-9.

[21]

Schieffelers DR, van Breda E, Gebruers N, Meirte J, Van Daele U. Status of adult inpatient burn rehabilitation in Europe: are we neglecting metabolic outcomes? Burns Trauma. 2021; 9: tkaa039.

[22]

ISBI Practice Guidelines Committee.ISBI practice guidelines for burn care. Burns. 2016; 42: 953-1021.

[23]

Palmieri T. ISBI practice guidelines committee.ISBI practice guidelines for burn care, part 2. Burns. 2018; 44: 1617-706.

[24]

European Burns Association.European practice guidelines for burn care: minimum level of burn care provision in Europe (Version 4), 2017.

[25]

Nedelec B, Serghiou MA, Niszczak J, McMahon M, Healey T. Practice guidelines for early ambulation of burn survivors after lower extremity grafts. J Burn Care Res. 2012; 33: 319-29.

[26]

Cartotto R, Johnson L, Rood JM, Lorello D, Matherly A, Parry I, et al. Clinical practice guideline: early mobilization and rehabilitation of critically ill burn patients. J Burn Care Res. 2022; 44: 1-15.

[27]

Cen Y, Chai J, Chen H, Chen J, Guo G, Han C, et al. Guidelines for burn rehabilitation in China. Burns Trauma. 2015; 3: 20.

[28]

Dombrecht D, Van Daele U, Van Asbroeck B, Schieffelers D, Guns P, Gebruers N, et al. Molecular mechanisms of postburn muscle wasting and the therapeutic potential of physical exercise. J Cachexia Sarcopenia Muscle 2023: jcsm.13188, 14, 758, 70.

[29]

Pedersen BK, Saltin B. Exercise as medicine-evidence for prescribing exercise as therapy in 26 different chronic diseases. Scand J Med Sci Sports. 2015; 25: 1-72.

[30]

Hermans G, Jonghe BD, Bruyninckx F, den Berghe GV. Interventions for preventing critical illness polyneuropathy and critical illness myopathy. Cochrane Database Syst Rev. 2014; 2014: CD006832.

[31]

Malin SK, Liu Z, Barrett EJ, Weltman A. Exercise resistance across the prediabetes phenotypes: impact on insulin sensitivity and substrate metabolism. Rev Endocr Metab Disord. 2016; 17: 81-90.

[32]

Kouidi E, Albani M, Natsis K, Megalopoulos A, Gigis P, Guiba-Tziampiri O, et al. The effects of exercise training on muscle atrophy in haemodialysis patients. Nephrol Dial Transplant. 1998; 13: 685-99.

[33]

Gittings PM, Wand BM, Hince DA, Grisbrook TL, Wood FM, Edgar DW. The efficacy of resistance training in addition to usual care for adults with acute burn injury: a randomised controlled trial. Burns. 2021; 47: 84-100.

[34]

Przkora R, Herndon DN, Suman OE. The effects of Oxandrolone and exercise on muscle mass and function in children with severe burns. Pediatrics. 2007; 119: e109-16.

[35]

Suman OE, Thomas SJ, Wilkins JP, Mlcak RP, Herndon DN. Effect of exogenous growth hormone and exercise on lean mass and muscle function in children with burns. J Appl Physiol. 2003; 94: 2273-81.

[36]

Suman OE, Spies RJ, Celis MM, Mlcak RP, Herndon DN. Effects of a 12-wk resistance exercise program on skeletal muscle strength in children with burn injuries. J Appl Physiol. 2001; 91: 1168-75.

[37]

Rivas E, Herndon DN, Porter C, Meyer W, Suman OE.Short-term metformin and exercise training effects on strength, aerobic capacity, glycemic control, and mitochondrial function in children with burn injury. Am J Physiol-Endocrinol Metab. 2018; 314: E232-40.

[38]

Schieffelers DR, Dombrecht D, Lafaire C, De Cuyper L, Rose T, Vandewal M, et al. Effects of exercise training on muscle wasting, muscle strength and quality of life in adults with acute burn injury. Burns. 2023; 49: 1602-13.

[39]

Deng H, Chen J, Li F, Li-Tsang CWP, Liu Q, Ma X, et al. Effects of mobility training on severe burn patients in the BICU: a retrospective cohort study. Burns. 2016; 42: 1404-12.

[40]

Baytieh L, Li F. Physiotherapeutic and dietetic parameters in burns patients modelling a multidisciplinary approach to burns practice: a bi-disciplinary illustration of interrelated factors. Burns. 2021; 47: 1094-101.

[41]

Okhovatian F, Zoubine N. A comparison between two burn rehabilitation protocols. Burns. 2007; 33: 429-34.

[42]

Jeschke MG, Mlcak RP, Finnerty CC, Norbury WB, Gauglitz GG, Kulp GA, et al. Burn size determines the inflammatory and hypermetabolic response. Crit Care. 2007; 11: R90.

[43]

Knuth CM, Auger C, Jeschke MG. Burn-induced hypermetabolism and skeletal muscle dysfunction. Am J Physiol Cell Physiol. 2021; 321: C58-71.

[44]

Stanojcic M, Abdullahi A, Rehou S, Parousis A, Jeschke MG. Pathophysiological response to burn injury in adults. Ann Surg. 2018; 267: 576-84.

[45]

Jeschke MG, Patsouris D, Stanojcic M, Abdullahi A, Rehou S, Pinto R, et al. Pathophysiologic response to burns in the elderly. EBioMedicine. 2015; 2: 1536-48.

[46]

Stanojcic M, Chen P, Xiu F, Jeschke MG. Impaired immune response in elderly burn patients: new insights into the immune-senescence phenotype. Ann Surg. 2016; 264: 195-202.

[47]

Peng X, Wang K, Zhang Y, Yan H, Wang C, Song L, et al. Establishment and assessment of new formulas for energy consumption estimation in adult burn patients. PLoS One. 2014; 9: e110409. https://doi.org/10.1371/journal.pone.0110409.

[48]

Sommers J, Engelbert RH, Dettling-Ihnenfeldt D, Gosselink R, Spronk PE, Nollet F, et al. Physiotherapy in the intensive care unit: an evidence-based, expert driven, practical statement and rehabilitation recommendations. Clin Rehabil. 2015; 29: 1051-63.

[49]

Taylor JD, Fletcher JP. Reliability of the 8-repetition maximum test in men and women. J Sci Med Sport. 2012; 15: 69-73.

[50]

Tapking C, Popp D, Herndon DN, Armenta AM, Branski LK, Murton AJ, et al. Cardiovascular effect of varying interval training frequency in rehabilitation of severely burned children. J Burn Care Res. 2019; 40: 34-8.

[51]

De Backer IC, Schep G, Hoogeveen A, Vreugdenhil G, Kester AD, van Breda E. Exercise testing and training in a cancer rehabilitation program: the advantage of the steep ramp test. Arch Phys Med Rehabil. 2007; 88: 610-6.

[52]

Garber CE, Blissmer B, Deschenes MR, Franklin BA, Lamonte MJ, Lee I-M, et al. Quantity and quality of exercise for developing and maintaining cardiorespiratory, musculoskeletal, and neuromotor fitness in apparently healthy adults: guidance for prescribing exercise. Med Sci Sports Exerc. 2011; 43: 1334-59.

[53]

American College of Sports Medicine.Progression models in resistance training for healthy adults. Med Sci Sports Exerc. 2009; 41: 687-708.

[54]

Gruther W, Benesch T, Zorn C, Paternostro-Sluga T, Quittan M, Fialka-Moser V, et al. Muscle wasting in intensive care patients: ultrasound observation of the m. quadriceps femoris muscle layer. J Rehabil Med. 2008; 40: 185-9.

[55]

Puthucheary ZA, Rawal J, McPhail M, Connolly B, Ratnayake G, Chan P, et al. Acute skeletal muscle wasting in critical illness. JAMA. 2013; 310: 1591-600.

[56]

Paris MT, Lafleur B, Dubin JA, Mourtzakis M. Development of a bedside viable ultrasound protocol to quantify appendicular lean tissue mass. J Cachexia Sarcopeni. 2017; 8: 713-26.

[57]

Pardo E, El Behi H, Boizeau P, Verdonk F, Alberti C, Lescot T. Reliability of ultrasound measurements of quadriceps muscle thickness in critically ill patients. BMC Anesthesiol. 2018; 18: 205.

[58]

Paris MT, Mourtzakis M, Day A, Leung R, Watharkar S, Kozar R, et al. Validation of bedside ultrasound of muscle layer thickness of the quadriceps in the critically ill patient (VALIDUM study): a prospective multicenter study. JPEN Parenter Enter. 2017; 41: 171-80.

[59]

Tourel C, Burnol L, Lanoiselé J, Molliex S, Viallon M, Croisille P, et al. Reliability of standardized ultrasound measurements of quadriceps muscle thickness in neurological critically ill patients: a comparison to computed tomography measures. J Rehabil Med. 2020; 52: 0.

[60]

Lambell KJ, Tierney AC, Wang JC, Nanjayya V, Forsyth A, Goh GS, et al. Comparison of ultrasound-derived muscle thickness with computed tomography muscle cross-sectional area on admission to the intensive care unit: a pilot cross-sectional study. JPEN Parenter Enter. 2020; 45: 136-45.

[61]

Schieffelers DR, Dombrecht D, Lafaire C, De Cuyper L, Rose T, Meirte J, et al. Reliability and feasibility of skeletal muscle ultrasound in the acute burn setting. Burns. 2023; 49: 68-79.

[62]

Abe T, Dabbs NC, Nahar VK, Ford MA, Bass MA, Loftin M. Relationship between dual-energy x-ray absorptiometry-derived appendicular lean tissue mass and total body skeletal muscle mass estimated by ultrasound. Int J Clin Med. 2013; 04: 283-6.

[63]

Gittings PM, Hince DA, Wand BM, Wood FM, Edgar DW. Grip and muscle strength dynamometry in acute burn injury: evaluation of an updated assessment protocol. J Burn Care Res Off Publ Am Burn Assoc. 2018; 39: 939-47.

[64]

Gittings P, Salet M, Burrows S, Ruettermann M, Wood FM, Edgar D. Grip and muscle strength dynamometry are reliable and valid in patients with unhealed minor burn wounds. J Burn Care Res. 2016; 37: 388-96.

[65]

Kildal M, Andersson G, Fugl-Meyer AR, Lannerstam K, Gerdin B. Development of a brief version of the burn specific health scale (BSHS-B). J Trauma. 2001; 51: 740-6.

[66]

Zhang LJ, Cao J, Lu J, Lu XY, Feng P, Xia ZF, et al. Development of quality of life scale in Chinese burn patients: Cross-cultural adaptation process of burn-specific health scale-brief. Burns. 2012; 38: 1216-23.

[67]

Luo N, Li M, Liu GG, Lloyd A, de Charro F, Herdman M. Developing the Chinese version of the new 5-level EQ-5D descriptive system: the response scaling approach. Qual Life Res. 2013; 22: 885-90.

[68]

Willebrand M, Kildal M. A simplified domain structure of the burn-specific health scale-brief (BSHS-B): a tool to improve its value in routine clinical work. J Trauma Acute Care Surg. 2008; 64: 1581-6.

[69]

Luo N, Liu G, Li M, Guan H, Jin X, Rand-Hendriksen K. Estimating an EQ-5D-5L value set for China. Value Health. 2017; 20: 662-9.

[70]

Meirte J, Van Daele U, Maertens K, Moortgat P, Deleus R, Van Loey NE. Convergent and discriminant validity of quality of life measures used in burn populations. Burns. 2017; 43: 84-92.

[71]

Spronk I, Legemate C, Oen I, van Loey N, Polinder S, van Baar M. Health related quality of life in adults after burn injuries: a systematic review. PLoS One. 2018; 13:e0197507. https://doi.org/10.1371/journal.pone.0197507.

[72]

Saghaei M, Saghaei S. Implementation of an open-source customizable minimization program for allocation of patients to parallel groups in clinical trials. J Biomed Sci Eng. 2011; 04: 734-9.

[73]

Hurvich CM, Tsai C-L. Regression and time series model selection in small samples. Biometrika. 1989; 76: 297-307.

[74]

Cambiaso-Daniel J, Malagaris I, Rivas E, Hundeshagen G, Voigt CD, Blears E, et al. Body composition changes in severely burned children during ICU hospitalization. Pediatr Crit Care Med. 2017; 18: e598-605.

[75]

Dombrecht D, Van Daele U, Van Asbroeck B, Schieffelers DR, Guns P-J, van Breda E. Skeletal muscle wasting after burn is regulated by a decrease in anabolic signaling in the early flow phase. Burns. 2023; 49: 1574-84.

[76]

Wilkinson SB, Phillips SM, Atherton PJ, Patel R, Yarasheski KE, Tarnopolsky MA, et al. Differential effects of resistance and endurance exercise in the fed state on signalling molecule phosphorylation and protein synthesis in human muscle. J Physiol. 2008; 586: 3701-17.

[77]

Graham ZA, Lavin KM, O’Bryan SM, Thalacker-Mercer AE, Buford TW, Ford KM, et al. Mechanisms of exercise as a preventative measure to muscle wasting. Am J Physiol-Cell Physiol. 2021; 321: C40-57.

[78]

Song J, Baer LA, Threlkeld MRS, Geng C, Wade CE, Wolf SE. Insulin and exercise improved muscle function in rats with severe burns and hindlimb unloading. Physiol Rep. 2019; 7: e14158.

[79]

Clark A, Imran J, Madni T, Wolf SE. Nutrition and metabolism in burn patients. Burns Trauma. 2017; 5: 11.

[80]

Demling RH. Nutrition, anabolism, and the wound healing process: an overview. Eplasty. 2009; 9: e9.

[81]

Zouhal H, Jayavel A, Parasuraman K, Hayes LD, Tourny C, Rhibi F, et al. Effects of exercise training on anabolic and catabolic hormones with advanced age: a systematic review. Sports Med. 2022; 52: 1353-68.

[82]

Wischmeyer PE, San-Millan I. Winning the war against ICU-acquired weakness: new innovations in nutrition and exercise physiology. Crit Care. 2015; 19: S6.

[83]

Flores O, Tyack Z, Stockton K, Ware R, Paratz JD. Exercise training for improving outcomes post-burns: a systematic review and meta-analysis. Clin Rehabil. 2018; 32: 734-46.

[84]

Gittings PM, Grisbrook TL, Edgar DW, Wood FM, Wand BM, O’Connell NE. Resistance training for rehabilitation after burn injury: a systematic literature review & meta-analysis. Burns. 2018; 44: 731-51.

[85]

Saeman MR, DeSpain K, Liu M-M, Carlson BA, Song J, Baer LA, et al. Effects of exercise on soleus in severe burn and muscle disuse atrophy. J Surg Res. 2015; 198: 19-26.

[86]

Badawy MM, Allam NM. Impact of adding protein supplementation to exercise training on lean body mass and muscle strength in burn patients. J Burn Care Res. 2021; 42: 968-74.

[87]

Fry CS, Porter C, Sidossis LS, Nieten C, Reidy PT, Hundeshagen G, et al. Satellite cell activation and apoptosis in skeletal muscle from severely burned children. J Physiol. 2016; 594: 5223-36.

[88]

Sehat A, Huebinger RM, Carlson DL, Zang QS, Wolf SE, Song J. Burn serum stimulates myoblast cell death associated with IL-6-induced mitochondrial fragmentation. Shock. 2017; 48: 236-42.

[89]

Corrick KL, Stec MJ, Merritt EK, Windham ST, Thomas SJ, Cross JM, et al. Serum from human burn victims impairs myogenesis and protein synthesis in primary myoblasts. Front Physiol. 2015; 6: 184.

[90]

Paratz JD, Stockton K, Plaza A, Muller M, Boots RJ. Intensive exercise after thermal injury improves physical, functional, and psychological outcomes. J Trauma Acute Care Surg. 2012; 73: 186-94.

[91]

Palackic A, Rego A, Parry I, Sen S, Branski LK, Hallman TG, et al. Effects of aerobic exercise in the intensive care unit on patient-reported physical function and mental health outcomes in severely burned children-a multicenter prospective randomized trial. J Pers Med. 2023; 13: 455.

[92]

Chen J, Li-Tsang CWP, Yan H, Liang G, Tan J, Yang S, et al. A survey on the current status of burn rehabilitation services in China. Burns. 2013; 39: 269-78.

[93]

Serghiou MA, Niszczak J, Parry I, Li-Tsang CWP, Van den Kerckhove E, Smailes S, et al. One world one burn rehabilitation standard. Burns. 2016; 42: 1047-58.

[94]

Xie WG. A long way for the popularization and improvement of burn rehabilitation. Chin J Burns. 2022; 38: 1105-9.

[95]

Cambiaso-Daniel J, Parry I, Rivas E, Kemp-Offenberg J, Sen S, Rizzo JA, et al. Strength and cardiorespiratory exercise rehabilitation for severely burned patients during intensive care units: a survey of practice. J Burn Care Res. 2018; 39: 897-901.

[96]

Flores O, Tyack Z, Stockton K, Paratz JD. The use of exercise in burns rehabilitation: a worldwide survey of practice. Burns. 2020; 46: 322-32.

[97]

Lim WC, Hill A-M, Edgar DW, Elliott M, van der Lee LM. Multidisciplinary staff perceived barriers and enablers to early mobilization of patients with burns in the ICU. Burns. 2023; 49: 1688-97.

[98]

Gomez DS, Mariani U, Ferreira MC. The problem of subepidermal blisters in neoformed integuments. Burns. 2005; 31: 811-3.

[99]

Glas GJ, Horn J, van der Hoeven SM, Hollmann MW, Cleffken B, Colpaert K, et al. Changes in ventilator settings and ventilation-induced lung injury in burn patients-a systematic review. Burns. 2020; 46: 762-70.

[100]

Smailes S, Spoors C, da Costa FM, Martin N, Barnes D.Early tracheostomy and active exercise programmes in adult intensive care patients with severe burns. Burns. 2022; 48: 1599-605.

[101]

Bright L, Van Der Lee L, Hince D, Wood FM, Edgar DW. Quantification of the negative impact of sedation and inotropic support on achieving early mobility in burn patients in ICU: a single center observational study. Burns. 2021; 47: 1756-65.

[102]

Xie WG. To analyze the past, present, and future of burn medicine from the sixty years of burn surgery in Hubei province. Chin J Burns. 2018; 34: 847-51.

[103]

Taverny G, Lescot T, Pardo E, Thonon F, Maarouf M, Alberti C. Outcomes used in randomised controlled trials of nutrition in the critically ill: a systematic review. Crit Care. 2019; 23: 12.

[104]

Boutron I, Tubach F, Giraudeau B, Ravaud P. Blinding was judged more difficult to achieve and maintain in non-pharmacologic than pharmacologic trials. J Clin Epidemiol. 2004; 57: 543-50.

[105]

Mathers J, Moiemen N, Bamford A, Gardiner F, Tarver J. Ensuring that the outcome domains proposed for use in burns research are relevant to adult burn patients: a systematic review of qualitative research evidence. Burns Trauma. 2020; 8: tkaa030.

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