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Transvenous phrenic nerve stimulation for treating central sleep apnea may regulate sleep microstructure.
Hartmann, Simon; Immanuel, Sarah; McKane, Scott; Linz, Dominik; Parrino, Liborio; Baumert, Mathias.
Afiliação
  • Hartmann S; Discipline of Psychiatry, Adelaide Medical School, The University of Adelaide, Adelaide, Australia.
  • Immanuel S; Discipline of Biomedical Engineering, School of Electrical and Mechanical Engineering, The University of Adelaide, Adelaide, Australia; School of Business Information Systems, Torrens University, Adelaide, Australia.
  • McKane S; ZOLL Respicardia, Inc., Minnetonka, MN, USA.
  • Linz D; Department of Cardiology, Maastricht University Medical Centre and Cardiovascular Research Institute, Maastricht, the Netherlands; Centre for Heart Rhythm Disorders, The University of Adelaide and Royal Adelaide Hospital, Adelaide, Australia; Department of Biomedical Sciences, Faculty of Health and
  • Parrino L; Sleep Disorders Center, Department of Neurology, University of Parma, Parma, Italy.
  • Baumert M; Discipline of Biomedical Engineering, School of Electrical and Mechanical Engineering, The University of Adelaide, Adelaide, Australia. Electronic address: mathias.baumert@adelaide.edu.au.
Sleep Med ; 113: 70-75, 2024 01.
Article em En | MEDLINE | ID: mdl-37988861
ABSTRACT
STUDY

OBJECTIVES:

To assess the impact of transvenous phrenic nerve stimulation (TPNS) on non-rapid eye movement sleep microstructure quantified by cyclic alternating pattern (CAP) in individuals with central sleep apnea (CSA).

METHODS:

We analyzed baseline and 6-month follow-up overnight polysomnograms (PSG) in 134 CSA patients enrolled in the remede System Pivotal Trial implanted with TPNS randomized (11) to neurostimulation (treatment group) or no stimulation (control group). Differences in CAP rate, A1 index, and A2+A3 index between study arms at follow-up were assessed using Analysis of Covariance adjusted for baseline values.

RESULTS:

On follow-up PSG, the treatment group showed a decrease in the frequency of A2+A3 phases compared to controls (-5.86 ± 11.82 vs. 0.67 ± 15.25, p = 0.006), while the frequency of A1 phases increased more in the treatment group (2.57 ± 11.67 vs. -2.47 ± 10.60, p = 0.011). The change in CAP rate at follow-up was comparable between study arms.

CONCLUSIONS:

TPNS treatment for central sleep apnea may affect sleep microstructure. Brief phases of rapid cortical activity appear to be replaced by short phases of slower cortical activity, which may promote sleep continuity. Further investigations are warranted to elucidate the mechanisms underlying the effect of TPNS on CAP.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia por Estimulação Elétrica / Apneia do Sono Tipo Central Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia por Estimulação Elétrica / Apneia do Sono Tipo Central Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article