Safety and feasibility of chronic transvenous phrenic nerve stimulation for treatment of central sleep apnea in heart failure patients

2015 ◽  
Vol 11 (2) ◽  
pp. 176-184 ◽  
Author(s):  
Xilong Zhang ◽  
Ning Ding ◽  
Buqing Ni ◽  
Bing Yang ◽  
Hong Wang ◽  
...  
2020 ◽  
Vol 26 (10) ◽  
pp. S67
Author(s):  
Lee R. Goldberg ◽  
Loreena Hill ◽  
Maria Rosa Costanzo ◽  
Ovidiu Chioncel ◽  
Mitja Lainscak ◽  
...  

2017 ◽  
Vol 38 (suppl_1) ◽  
Author(s):  
M.R. Costanzo ◽  
P. Ponikowski ◽  
S. Javaheri ◽  
R. Augostini ◽  
L. Goldberg ◽  
...  

2021 ◽  
Vol 10 (2) ◽  
pp. 202
Author(s):  
Max Potratz ◽  
Christian Sohns ◽  
Daniel Dumitrescu ◽  
Philipp Sommer ◽  
Henrik Fox

Background: Central sleep apnea (CSA) is a common comorbidity in patients with heart failure (HF) and has been linked to increased morbidity and mortality risk. In addition, CSA is associated with impaired quality of life, reduced physical performance capacity, and hypoxemia. Phrenic nerve stimulation (PNS) is a novel approach to the treatment of CSA and has been shown to be safe and effective in this indication. However, there are currently no data on the effects of PNS on physical performance and hypoxia in CSA HF patients, both of which have been shown to be linked to mortality in HF. Methods: This prospective study enrolled patients with HF and CSA diagnosed using polysomnography. All were implanted with a PNS system (remedē® system, Respicardia Inc., Minnetonka, MN, USA) for the treatment of CSA. Examinations included polysomnography (to determine hypoxemic burden), echocardiography and a standardized 6-min walk test prior to device implantation (baseline) and after 6 months of follow-up. Results: A total of 24 patients were enrolled (mean age 67.1 ± 11.2 years, 88% male). The 6-min walk distance was 369.5 ± 163.5 m at baseline and significantly improved during follow-up (to 410 ± 169.7 m; p = 0.035). Hypoxemic burden, determined based on time with oxygen saturation < 90% improved from 81 ± 55.8 min at baseline to 27.9 ± 42.8 min during PNS therapy (p < 0.01). Conclusion: In addition to safely and effectively treating CSA, PNS is also associated with improved physical performance capacity and reduced hypoxemic burden in patients with HF.


2012 ◽  
Vol 9 (1) ◽  
pp. 53-56 ◽  
Author(s):  
Sitaramesh Emani ◽  
William T Abraham

Central sleep apnea (CSA) is a prominent co-morbidity in heart failure (HF) resulting from dysregulated neurological responses to abnormal carbon dioxide levels. The presence of CSA in HF has been linked with deleterious physiological changes and is associated with increased mortality, yet treatment options for CSA in HF are currently lacking. This article briefly reviews the mechanisms of CSA in HF as well as the available evidence on present therapies, and describes phrenic nerve stimulation as a potential novel therapeutic approach.


2012 ◽  
Vol 18 (8) ◽  
pp. S14-S15
Author(s):  
William T. Abraham ◽  
Olaf Oldenburg ◽  
Piotr Ponikowski ◽  
Alan Schwartz ◽  
Bradley Bart ◽  
...  

CHEST Journal ◽  
2020 ◽  
Vol 158 (4) ◽  
pp. A2337
Author(s):  
Shahrokh Javaheri ◽  
Scott McKane ◽  
Timothy Meyer ◽  
Robin Germany ◽  
Lee Goldberg

SLEEP ◽  
2020 ◽  
Vol 43 (Supplement_1) ◽  
pp. A270-A271
Author(s):  
S Javaheri ◽  
S McKane ◽  
T E Meyer ◽  
R Germany

Abstract Introduction Some subjects with central sleep apnea (CSA) complain of subjective excessive daytime sleepiness (EDS), as assessed by the Epworth Sleepiness Score (ESS). However, there is considerable variability in the level of chances of dozing for each of the 8 ESS questions, as each reflects a different situation. The aim of this analysis was to examine individual situations of the ESS and determine if transvenous phrenic nerve stimulation (TPNS) resulted in improvements of individual ESS situations which were scored moderate to high (2 and 3) at baseline. Patient Global Assessment (PGA) was also assessed. Methods All 151 subjects enrolled in the randomized (Treatment vs Control) remedē System pivotal trial were included in the analysis. All subjects were implanted, but activation in Control arm was delayed 6 months. Results Greater than or equal to 50% of patients scored moderate-high on several individual ESS situations: chance of dozing while sitting and reading (57%), watching television (62%), while lying down to rest in the afternoon when circumstances permit (76%). In the active arm, 68%, 44% and 29% of patients with moderate-high at baseline, respectively, for sitting and reading, watching television, and lying down to rest in the afternoon shifted to less than moderate at 6 months. Respective shifts for the control arm were 29%, 23% and 13%. Seventy-two percent of treated subjects with baseline ESS&gt;10 shifted to ≤10 at 6 months compared to 26% of control patients. Additionally, 72% of treated compared to 7% of control subjects with baseline ESS&gt;10 reported markedly or moderately improved QoL. Conclusion Results of this randomized controlled trial shows that compared to the control arm, TPNS leads to improvements in various situations of the ESS as well as QoL. The most improved situations were less chance of dozing while reading and watching television. Support Respicardia


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