Neuromuscular electrical stimulation in early rehabilitation of patients with postoperative complications after cardiovascular surgery: A randomized controlled trial

Alexey Nikolaevich Sumin, Pavel Alexandrovich Oleinik, Andrey Viktorovich Bezdenezhnykh, Anna Valeryvena Ivanova, Alexey Nikolaevich Sumin, Pavel Alexandrovich Oleinik, Andrey Viktorovich Bezdenezhnykh, Anna Valeryvena Ivanova

Abstract

Background: To evaluate the effectiveness of neuromuscular electrical stimulation (NMES) in early rehabilitation of patients with postoperative complications after cardiovascular surgery.

Methods: 37 patients (25 men and 12 women) aged 45 to 70 years with postoperative complications after cardiovascular surgery were included in the study. Eighteen patients underwent NMES daily since postoperative day 3 until discharge in addition to standard rehabilitation program (NMES group), and 19 patients underwent standard rehabilitation program only (non-NMES group). The primary outcome was the knee extensors strength at discharge in NMES group and in control. Secondary outcomes were the handgrip strength, knee flexor strength, and cross-sectional area (CSA) of the quadriceps femoris in groups at discharge.

Results: Baseline characteristics were not different between the groups. Knee extensors strength at discharge was significantly higher in the NMES group (28.1 [23.8; 36.2] kg on the right and 27.45 [22.3; 33.1] kg on the left) than in the non-NMES group (22.3 [20.1; 27.1] and 22.5 [20.1; 25.9] kg, respectively; P < .001). Handgrip strength, knee flexor strength, quadriceps CSA, and 6 minute walk distance at discharge in the groups had no significant difference.

Conclusions: This pilot study shows a beneficial effect of NMES on muscle strength in patients with complications after cardiovascular surgery. The use of NMES showed no effect on strength of non-stimulated muscle, quadriceps CSA, and distance of 6-minute walk test at discharge.Further blind randomized controlled trials should be performed with emphasis on the effectiveness of NEMS in increasing muscle strength and structure in these patients.

Conflict of interest statement

The authors have no conflicts of interest to disclose.

Figures

Figure 1
Figure 1
Flow diagram of study participants; NMES = neuromuscular electrical stimulation.
Figure 2
Figure 2
Knee extensor strength at POD 3 and discharge in NMES (n = 18) and control (n = 19) groups. ∗Between Baseline and Discharge in the Group; ∗∗Between Groups in Baseline or in Discharge. NMES = neuromuscular electrical stimulation, POD = postoperative day.
Figure 3
Figure 3
Knee flexor strength at POD 3 and discharge in NMES (n = 18) and control (n = 19) groups. ∗Between Baseline and Discharge in the Group; ∗∗Between Groups in Baseline or in Discharge. NMES = neuromuscular electrical stimulation, POD = postoperative day.
Figure 4
Figure 4
Handgrip strength at POD 3 and discharge in NMES (n = 18) and control (n = 19) groups. ∗Between Baseline and Discharge in the Group; ∗∗Between Groups in Baseline or in Discharge. NMES = neuromuscular electrical stimulation, POD = postoperative day.
Figure 5
Figure 5
Quadriceps muscle cross-sectional area at POD 3 and discharge in NMES (n = 18) and control (n = 19) groups. ∗Between Baseline and Discharge in the Group; ∗∗Between Groups in Baseline or in Discharge. NMES = neuromuscular electrical stimulation, POD = postoperative day.

References

    1. Iida Y, Yamazaki T, Arima H, et al. Predictors of surgery-induced muscle proteolysis in patients undergoing cardiac surgery. J Cardiol 2016;68:536–41.
    1. Bloch SA, Lee JY, Wort SJ, et al. Sustained elevation of circulating growth and differentiation factor-15 and a dynamic imbalance in mediators of muscle homeostasis are associated with the development of acute muscle wasting following cardiac surgery. Crit Care Med 2013;41:982–9.
    1. Iida Y, Yamazaki T, Kawabe T, et al. Postoperative muscle proteolysis affects systemic muscle weakness in patients undergoing cardiac surgery. Int J Cardiol 2014;172:595–7.
    1. Gomes Neto M, Oliveira FA, Reis HF, et al. Effects of neuromuscular electrical stimulation on physiologic and functional measurements in patients with heart failure: a systematic review with meta-analysis. J Cardiopulm Rehabil Prev 2016;36:157–66.
    1. Paillard T. Muscle plasticity of aged subjects in response to electrical stimulation training and inversion and/or limitation of the sarcopenic process. Ageing Res Rev 2018;46:1–3.
    1. Iwatsu K, Yamada S, Iida Y, et al. Feasibility of neuromuscular electrical stimulation immediately after cardiovascular surgery. Arch Phys Med Rehabil 2015;96:63–8.
    1. Bezdenezhnykh AV, Sumin AN, Olejnik PA. The first experience of electrical myostimulation for early rehabilitation of the heart transplant recipient with complicated postoperative period. Complex Issues of Cardiovascular Diseases 2018;7(4S):146–50.
    1. Iwatsu K, Iida Y, Kono Y, et al. Neuromuscular electrical stimulation may attenuate muscle proteolysis after cardiovascular surgery: a preliminary study. J Thorac Cardiovasc Surg 2017;153:373–9.e1.
    1. Kitamura H, Yamada S, Adachi T, et al. Effect of perioperative neuromuscular electrical stimulation in patients undergoing cardiovascular surgery: a pilot randomized controlled trial. Semin Thorac Cardiovasc Surg 2019;31:361–7.
    1. Mandal S, Suh E, Thompson A, et al. Comparative study of linear and curvilinear ultrasound probes to assess quadriceps rectus femoris muscle mass in healthy subjects and in patients with chronic respiratory disease. BMJ Open Resp Res 2016;3:e000103.
    1. Fontes Cerqueira TC, Cerqueira Neto ML, Cacau LAP, et al. Ambulation capacity and functional outcome in patients undergoing neuromuscular electrical stimulation after cardiac valve surgery: a randomised clinical trial. Medicine (Baltimore) 2018;97:e13012.
    1. Fischer A, Spiegl M, Altmann K, et al. Muscle mass, strength and functional outcomes in critically ill patients after cardiothoracic surgery: does neuromuscular electrical stimulation help? The Catastim 2 randomized controlled trial. Crit Care 2016;20:30.
    1. Medrinal C, Combret Y, Prieur G, et al. Comparison of exercise intensity during four early rehabilitation techniques in sedated and ventilated patients in ICU: a randomised cross-over trial. Crit Care 2018;22:110.
    1. Paillard T. Training based on electrical stimulation superimposed onto voluntary contraction would be relevant only as part of submaximal contractions in healthy subjects. Front Physiol 2018;9:1428.
    1. da Cunha RA, Pinfildi CE, de Castro Pochini A, et al. Photobiomodulation therapy and NMES improve muscle strength and jumping performance in young volleyball athletes: a randomized controlled trial study in Brazil. Lasers Med Sci 2020;35:621–31.
    1. Adams GR, Harris RT, Woodard D, et al. Mapping of electrical muscle stimulation using MRI. J Appl Physiol 1993;74:532–7.
    1. Mancinelli R, Toniolo L, Di Filippo ES, et al. Neuromuscular electrical stimulation induces skeletal muscle fiber remodeling and specific gene expression profile in healthy elderly. Front Physiol 2019;10:1459.
    1. Maffiuletti NA, Zory R, Miotti D, et al. Neuromuscular adaptations to electrostimulation resistance training. Am J Phys Med Rehabil 2006;85:167–75.
    1. Natsume T, Ozaki H, Kakigi R, et al. Effects of training intensity in electromyostimulation on human skeletal muscle. Eur J Appl Physiol 2018;118:1339–47.
    1. Song Y, Forsgren S, Yu J, et al. Effects on contralateral muscles after unilateral electrical muscle stimulation and exercise. PLoS One 2012;7:e52230.
    1. Frazer AK, Pearce AJ, Howatson G, et al. Determining the potential sites of neural adaptation to cross-education: implications for the cross-education of muscle strength. Eur J Appl Physiol 2018;118:1751–72.
    1. Gondin J, Guette M, Ballay Y, et al. Electromyostimulation training effects on neural drive and muscle architecture. Med Sci Sports Exerc 2005;37:1291–9.

Source: PubMed

3
Abonneren