Effect of CPAP Versus APAP in Patients With Obesity Undergoing Bariatric Surgery Protocol
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: In the intervention group, patients will be treated with auto-adjusting APAP, providing variable pressures throughout the sleep hours., CPAP.
- Who it may be relevant to
- Registry conditions: Sleep Apnea, Obstructive, Bariatric Surgery, Obesity, Treatment Adherence and Compliance. Basic parameters: 18 years — 80 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Spain
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Introduction Obstructive sleep apnea (OSA) is a common disorder in obese patients, especially those undergoing bariatric surgery. OSA is characterized by upper airway obstruction during sleep, leading to intermittent hypoxia and sleep fragmentation. Obesity and OSA are closely related conditions that can exacerbate each other. Positive airway pressure therapy is essential for managing OSA, but adherence to therapy can be challenging, particularly in patients who experience rapid physiological changes after bariatric surgery. Objective This study aims to determine whether automatic positive airway pressure therapy (APAP) improves nightly usage hours compared to continuous positive airway pressure therapy (CPAP) in obese patients undergoing bariatric surgery. Secondary objectives include evaluating the percentage of nights with therapy use over 4 hours, reduction of the residual apnea-hypopnea index (AHI), changes in daytime sleepiness, pressure requirements, side effects, sleep-related quality of life, reduction in in-person visits, and optimization of healthcare resources. Methodology A randomized, parallel-group, open-label, controlled clinical trial will be conducted. Adult patients eligible for bariatric surgery with a diagnosis of moderate to severe OSA (AHI \> 15) requiring positive pressure therapy will be included. Participants will be randomized to receive either APAP or CPAP. Follow-up will be conducted over 12 months after surgery, with assessments at 3, 6, and 12 months. Data will be collected on treatment adherence, residual AHI, OSA symptoms, daytime sleepiness, quality of life, and treatment costs. APAP therapy is expected to improve nightly usage hours compared to CPAP. It is also expected that APAP will show better adaptation to changing pressure needs after bariatric surgery. Data will be analyzed to evaluate the effectiveness and cost-efficiency of both therapies. This study will provide evidence on the efficacy of APAP compared to CPAP in obese patients undergoing bariatric surgery. The results will help optimize the treatment of OSA in this population and improve patients' quality of life. Additionally, the study is expected to contribute to the optimization of healthcare resources by reducing in-person visits and repeated sleep studies.
Interventions
- Device In the intervention group, patients will be treated with auto-adjusting APAP, providing variable pressures throughout the sleep hours.
AutoCPAP will be prescribed to patients undergoing bariatric surgery. - Device CPAP
In the control group, patients will be treated with CPAP.
Primary outcome measures
- APAP vs. CPAP: Impact on Nightly Usage in Obese Patients Undergoing Bariatric Surgery [Time frame: Obese patients undergoing bariatric surgery will be evaluated during the 3 months prior to surgery and at 3, 6, and 12 months postoperatively in patients with OSA undergoing bariatric surgery.]
Secondary outcome measures (11)
- Therapy Adherence Over Time [Time frame: 3 months before bariatric surgery and at 3, 6, and 12 months postoperatively.]
- Reduction in Residual AHI [Time frame: 3 months before bariatric surgery and at 3, 6, and 12 months postoperatively.]
- Daytime Sleepiness [Time frame: 3, 6, and 12 months postoperatively]
- Pressure Requirement Trends [Time frame: (3 months pre-surgery and 3, 6, and 12 months postoperatively).]
- Pressure Adaptability of APAP [Time frame: 3, 6, and 12 months postoperatively]
- Side Effects Monitoring [Time frame: (3 months pre-surgery and 3, 6, and 12 months postoperatively).]
- Sleep Quality (assessed using the Pittsburgh Sleep Quality Index) [Time frame: (3 months pre-surgery and 3, 6, and 12 months postoperatively).]
- General Quality of Life (assessed using the EuroQol-5D) [Time frame: 3 months pre-surgery and 3, 6, and 12 months postoperatively.]
- Reduction in Outpatient Visits [Time frame: (3 months pre-surgery and 3, 6, and 12 months postoperatively).]
- Healthcare Resource Optimization [Time frame: (3 months pre-surgery and 3, 6, and 12 months postoperatively).]
- STOP-BANG Questionnaire Accuracy [Time frame: (3 months pre-surgery and 3, 6, and 12 months postoperatively).]
Eligibility criteria
Inclusion criteria
- Subjects aged 18 to 80 years who meet the criteria for bariatric surgery and are on the surgical waiting list after approval by the bariatric surgery committee (BMI ≥35, or BMI ≥30 with comorbidities).
- Diagnosis of moderate or severe sleep apnea, defined by an Apnea-Hypopnea Index (AHI) >15, requiring treatment according to protocol ("Patients with an AHI of 15 or higher will be treated with CPAP if they have hypertension, excessive daytime sleepiness, or sleep-related symptoms not explained by other causes" \[17\]).
- Patients must be able to read and understand the informed consent and provide signed consent.
Exclusion criteria
- Patients with central sleep apnea or periodic breathing
- Patients with any active neoplasm
- Patients with severe uncontrolled psychiatric disorders, alcoholism, or active drug addiction
- Patients with unacceptable surgical/anesthetic risk
- Patients who have undergone previous surgery for OSA or who have been treated with positive airway pressure and did not tolerate it
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Spain · 1 center
- Hospital Universitario Ramón y Cajal, — Madrid
Publications
- Kermelly SB, Lajoie AC, Boucher ME, Series F. Impact of continuous positive airway pressure mode on adherence to treatment in obstructive sleep apnea patients awaiting bariatric surgery. J Sleep Res. 2021 Oct;30(5):e13288. doi: 10.1111/jsr.13288. Epub 2021 Feb 6. PMID 33547713
- Katasani T, Holt G, Al-Khyatt W, Idris I. Peri- and Postoperative Outcomes for Obstructive Sleep Apnoea Patients after Bariatric Surgery-a Systematic Review and Meta-analysis. Obes Surg. 2023 Jul;33(7):2016-2024. doi: 10.1007/s11695-023-06557-8. Epub 2023 May 4. PMID 37140722
- Collen J, Lettieri CJ, Eliasson A. Postoperative CPAP use impacts long-term weight loss following bariatric surgery. J Clin Sleep Med. 2015 Mar 15;11(3):213-7. doi: 10.5664/jcsm.4528. PMID 25515283
- de Raaff CAL, de Vries N, van Wagensveld BA. Obstructive sleep apnea and bariatric surgical guidelines: summary and update. Curr Opin Anaesthesiol. 2018 Feb;31(1):104-109. doi: 10.1097/ACO.0000000000000542. PMID 29176373
- Joosten SA, Hamilton GS, Naughton MT. Impact of Weight Loss Management in OSA. Chest. 2017 Jul;152(1):194-203. doi: 10.1016/j.chest.2017.01.027. Epub 2017 Feb 6. PMID 28185772
- Kapur VK, Auckley DH, Chowdhuri S, Kuhlmann DC, Mehra R, Ramar K, Harrod CG. Clinical Practice Guideline for Diagnostic Testing for Adult Obstructive Sleep Apnea: An American Academy of Sleep Medicine Clinical Practice Guideline. J Clin Sleep Med. 2017 Mar 15;13(3):479-504. doi: 10.5664/jcsm.6506. PMID 28162150
- Xu YX, Wang SS, Wan YH, Su PY, Tao FB, Sun Y. Association of sleep fragmentation with general and abdominal obesity: a population-based longitudinal study. Int J Obes (Lond). 2024 Sep;48(9):1258-1265. doi: 10.1038/s41366-024-01547-x. Epub 2024 May 28. PMID 38806646
- Mediano O, Gonzalez Mangado N, Montserrat JM, Alonso-Alvarez ML, Almendros I, Alonso-Fernandez A, Barbe F, Borsini E, Caballero-Eraso C, Cano-Pumarega I, de Carlos Villafranca F, Carmona-Bernal C, Carrillo Alduenda JL, Chiner E, Cordero Guevara JA, de Manuel L, Duran-Cantolla J, Farre R, Franceschini C, Gaig C, Garcia Ramos P, Garcia-Rio F, Garmendia O, Gomez Garcia T, Gonzalez Pondal S, Hoyo Rodr PMID 33875282
Identifiers
NCT: NCT07001215 · 111/25