Transvenous phrenic nerve stimulation for the treatment of central sleep apnea reduces episodic hypoxemic burden

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Transvenous phrenic nerve stimulation for the treatment of central sleep apnea reduces episodic hypoxemic burden. / Baumert, Mathias; Immanuel, Sarah; McKane, Scott; Linz, Dominik.

In: International Journal of Cardiology, Vol. 378, 2023, p. 89-95.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Baumert, M, Immanuel, S, McKane, S & Linz, D 2023, 'Transvenous phrenic nerve stimulation for the treatment of central sleep apnea reduces episodic hypoxemic burden', International Journal of Cardiology, vol. 378, pp. 89-95. https://doi.org/10.1016/j.ijcard.2023.02.041

APA

Baumert, M., Immanuel, S., McKane, S., & Linz, D. (2023). Transvenous phrenic nerve stimulation for the treatment of central sleep apnea reduces episodic hypoxemic burden. International Journal of Cardiology, 378, 89-95. https://doi.org/10.1016/j.ijcard.2023.02.041

Vancouver

Baumert M, Immanuel S, McKane S, Linz D. Transvenous phrenic nerve stimulation for the treatment of central sleep apnea reduces episodic hypoxemic burden. International Journal of Cardiology. 2023;378:89-95. https://doi.org/10.1016/j.ijcard.2023.02.041

Author

Baumert, Mathias ; Immanuel, Sarah ; McKane, Scott ; Linz, Dominik. / Transvenous phrenic nerve stimulation for the treatment of central sleep apnea reduces episodic hypoxemic burden. In: International Journal of Cardiology. 2023 ; Vol. 378. pp. 89-95.

Bibtex

@article{ce93c85dd77a4737a5efcfcdcca1790e,
title = "Transvenous phrenic nerve stimulation for the treatment of central sleep apnea reduces episodic hypoxemic burden",
abstract = "Study objectives: To determine the effect of transvenous phrenic nerve stimulation (TPNS) on the composition of the nocturnal hypoxemic burden in patients with CSA. Methods: We analysed oximetry data from baseline and follow-up overnight polysomnograms (PSG) in 134 CSA patients with implanted TPNS randomised (1:1) to neurostimulation (treatment group; TPNS on) or no stimulation (control group; TPNS off) from the remedē System Pivotal Trial. The hypoxemic burden was quantified using a battery of metrics, including the oxygen desaturation index (ODI), the relative sleep time spent below 90% SpO2 (T90) due to acute episodic desaturations (T90desat) and due to non-specific and non-cyclic drifts of SpO2 (T90non-specific). Mean change from baseline is provided. Results: TPNS titrated to reduce respiratory events significantly reduced the ODI in the treatment group by −15.85 h−1 ± 1.99 compared to the control group, which increased 1.32 h−1 ± 1.85 (p 〈0001) and shortened the relative T90 duration by −3.81 percentage points ± 1.23 vs. 0.49 percentage points ± 1.14 increase (p = 0.012). This shortening of T90 was primarily accomplished by reducing the brief cyclic desaturations (T90desaturation: −4.32 percentage points ± 0.98 vs. 0.52 percentage points ± 0.91, p = 0.0004) while notable non-specific drifts in SpO2 remained unchanged (T90non-specific: 0.18 percentage points ± 0.62 vs. -0.13 percentage points ± 0.57, p = 0.72). Conclusions: TPNS appears to significantly reduce the nocturnal hypoxemic burden due to sleep-disordered breathing, but a considerable nocturnal hypoxemic burden from other sources remains. Further investigations are warranted to identify the best strategy to reduce the nocturnal hypoxemic burden beyond preventing respiratory events.",
keywords = "Central sleep apnea, Hypoxemic burden, Transvenous phrenic nerve stimulation",
author = "Mathias Baumert and Sarah Immanuel and Scott McKane and Dominik Linz",
note = "Publisher Copyright: {\textcopyright} 2023 The Author(s)",
year = "2023",
doi = "10.1016/j.ijcard.2023.02.041",
language = "English",
volume = "378",
pages = "89--95",
journal = "International Journal of Cardiology",
issn = "0167-5273",
publisher = "Elsevier Ireland Ltd",

}

RIS

TY - JOUR

T1 - Transvenous phrenic nerve stimulation for the treatment of central sleep apnea reduces episodic hypoxemic burden

AU - Baumert, Mathias

AU - Immanuel, Sarah

AU - McKane, Scott

AU - Linz, Dominik

N1 - Publisher Copyright: © 2023 The Author(s)

PY - 2023

Y1 - 2023

N2 - Study objectives: To determine the effect of transvenous phrenic nerve stimulation (TPNS) on the composition of the nocturnal hypoxemic burden in patients with CSA. Methods: We analysed oximetry data from baseline and follow-up overnight polysomnograms (PSG) in 134 CSA patients with implanted TPNS randomised (1:1) to neurostimulation (treatment group; TPNS on) or no stimulation (control group; TPNS off) from the remedē System Pivotal Trial. The hypoxemic burden was quantified using a battery of metrics, including the oxygen desaturation index (ODI), the relative sleep time spent below 90% SpO2 (T90) due to acute episodic desaturations (T90desat) and due to non-specific and non-cyclic drifts of SpO2 (T90non-specific). Mean change from baseline is provided. Results: TPNS titrated to reduce respiratory events significantly reduced the ODI in the treatment group by −15.85 h−1 ± 1.99 compared to the control group, which increased 1.32 h−1 ± 1.85 (p 〈0001) and shortened the relative T90 duration by −3.81 percentage points ± 1.23 vs. 0.49 percentage points ± 1.14 increase (p = 0.012). This shortening of T90 was primarily accomplished by reducing the brief cyclic desaturations (T90desaturation: −4.32 percentage points ± 0.98 vs. 0.52 percentage points ± 0.91, p = 0.0004) while notable non-specific drifts in SpO2 remained unchanged (T90non-specific: 0.18 percentage points ± 0.62 vs. -0.13 percentage points ± 0.57, p = 0.72). Conclusions: TPNS appears to significantly reduce the nocturnal hypoxemic burden due to sleep-disordered breathing, but a considerable nocturnal hypoxemic burden from other sources remains. Further investigations are warranted to identify the best strategy to reduce the nocturnal hypoxemic burden beyond preventing respiratory events.

AB - Study objectives: To determine the effect of transvenous phrenic nerve stimulation (TPNS) on the composition of the nocturnal hypoxemic burden in patients with CSA. Methods: We analysed oximetry data from baseline and follow-up overnight polysomnograms (PSG) in 134 CSA patients with implanted TPNS randomised (1:1) to neurostimulation (treatment group; TPNS on) or no stimulation (control group; TPNS off) from the remedē System Pivotal Trial. The hypoxemic burden was quantified using a battery of metrics, including the oxygen desaturation index (ODI), the relative sleep time spent below 90% SpO2 (T90) due to acute episodic desaturations (T90desat) and due to non-specific and non-cyclic drifts of SpO2 (T90non-specific). Mean change from baseline is provided. Results: TPNS titrated to reduce respiratory events significantly reduced the ODI in the treatment group by −15.85 h−1 ± 1.99 compared to the control group, which increased 1.32 h−1 ± 1.85 (p 〈0001) and shortened the relative T90 duration by −3.81 percentage points ± 1.23 vs. 0.49 percentage points ± 1.14 increase (p = 0.012). This shortening of T90 was primarily accomplished by reducing the brief cyclic desaturations (T90desaturation: −4.32 percentage points ± 0.98 vs. 0.52 percentage points ± 0.91, p = 0.0004) while notable non-specific drifts in SpO2 remained unchanged (T90non-specific: 0.18 percentage points ± 0.62 vs. -0.13 percentage points ± 0.57, p = 0.72). Conclusions: TPNS appears to significantly reduce the nocturnal hypoxemic burden due to sleep-disordered breathing, but a considerable nocturnal hypoxemic burden from other sources remains. Further investigations are warranted to identify the best strategy to reduce the nocturnal hypoxemic burden beyond preventing respiratory events.

KW - Central sleep apnea

KW - Hypoxemic burden

KW - Transvenous phrenic nerve stimulation

UR - http://www.scopus.com/inward/record.url?scp=85149701710&partnerID=8YFLogxK

U2 - 10.1016/j.ijcard.2023.02.041

DO - 10.1016/j.ijcard.2023.02.041

M3 - Journal article

C2 - 36841294

AN - SCOPUS:85149701710

VL - 378

SP - 89

EP - 95

JO - International Journal of Cardiology

JF - International Journal of Cardiology

SN - 0167-5273

ER -

ID: 340363835