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Peripheral electrical stimulation reduces postoperative hypoxemia in patients at risk for obstructive sleep apnea: a randomized-controlled trial.
Smith, Hugh M; Kilger, Joan; Burkle, Christopher M; Schroeder, Darrell R; Gali, Bhargavi.
Affiliation
  • Smith HM; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, 200 First Street, SW, Rochester, MN, 55905, USA. Smith.Hugh2@Mayo.edu.
  • Kilger J; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, 200 First Street, SW, Rochester, MN, 55905, USA.
  • Burkle CM; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, 200 First Street, SW, Rochester, MN, 55905, USA.
  • Schroeder DR; Department of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, USA.
  • Gali B; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, 200 First Street, SW, Rochester, MN, 55905, USA.
Can J Anaesth ; 66(11): 1296-1309, 2019 Nov.
Article in En | MEDLINE | ID: mdl-31338807
ABSTRACT

PURPOSE:

Severity of hypoxemic events resulting from obstructive sleep apnea (OSA) is correlated with increased risk of complications and sudden death. We studied the use of a peripheral transcutaneous electrical stimulus (TES) on the magnitude and duration of sleep apnea associated hypoxemia in postoperative patients at high risk for OSA.

METHODS:

In this randomized, double-blind, controlled, single-centre trial, 106 adult patients undergoing elective surgery who were at medium to high risk for OSA (sleep apnea clinical scores of 18-35) were randomized to either TES (active stimulus group, n = 53) or control (non-stimulus group, n = 53) during their stay in the postanesthesia care unit. Transcutaneous electrical stimuli were delivered at threshold oxygen saturation measurements (SpO2) ≤ 93%. The primary endpoint was the SpO2 area under the curve (AUC) < 90%. Secondary endpoints included the percentage of patients with SpO2 < 90%, duration SpO2 < 90%, lowest SpO2 in the first hour, and adverse events associated with TES.

RESULTS:

Compared with controls (n = 45), those in the active group (n = 34) showed a decreased SpO2 AUC < 90% (median 0.0 vs 15.2 % sec, respectively; P = 0.009), a smaller percentage of subjects with SpO2 < 90% (47% active vs 71% control; P = 0.03), a shorter duration of SpO2 < 90% (median 0.0 vs 19.1 sec, respectively; P = 0.01), and a higher nadir of SpO2 recorded during the first hour (median 90.5% vs 87.9%, respectively; P = 0.04). Among patients with at least one SpO2 < 93%, there were fewer with SpO2 < 90% in the active group (55% vs 84%, respectively; P = 0.009). No adverse events related to TES were reported.

CONCLUSION:

In postoperative surgical patients at risk for OSA, peripheral transcutaneous electrical stimulation applied during apneic episodes decreased the duration and magnitude of hypoxemia. TRIAL REGISTRATION www.ClinicalTrials.gov (NCT02554110); registered 18 September, 2015.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Postoperative Complications / Sleep Apnea, Obstructive / Electric Stimulation / Hypoxia Type of study: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Can J Anaesth Journal subject: ANESTESIOLOGIA Year: 2019 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Postoperative Complications / Sleep Apnea, Obstructive / Electric Stimulation / Hypoxia Type of study: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Can J Anaesth Journal subject: ANESTESIOLOGIA Year: 2019 Document type: Article Affiliation country: United States
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