Lachlan Stranks, Mohammad Abdulsalam, David O'Regan, Joerg Steier, Alanna Hare
{"title":"声学衍生的家庭睡眠研究诊断成人智力障碍阻塞性睡眠呼吸暂停:可行性研究。","authors":"Lachlan Stranks, Mohammad Abdulsalam, David O'Regan, Joerg Steier, Alanna Hare","doi":"10.1111/jir.70000","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Adults with intellectual disabilities (IDs) face significant health inequalities and reduced life expectancy compared to the general population. Sleep disorders, including obstructive sleep apnoea (OSA), are highly prevalent in this population; however, standard diagnostic modalities may be poorly tolerated and many people may remain undiagnosed. The aim of this study was to assess the feasibility of using an acoustic-derived home-based sleep study to diagnose OSA in adults with ID who were unable to tolerate standard inpatient or home sleep studies.</p><p><strong>Method: </strong>This was a prospective feasibility study (GSTT/2024/15803). Participants were identified from two tertiary outpatient sleep departments in London, UK. Eligible participants were aged ≥ 17 years with a diagnosed ID. Inpatient or existing home studies had not been tolerated or had been declined. Participants wore a small diagnostic sensor, the AcuPebble SA100 (Acurable Ltd., London, UK) for one to two nights in their own home. Baseline symptom screening and quality of life questionnaires were administered. Semiqualitative and qualitative feedback was obtained from participants. The primary outcome was successful completion of testing, defined as ≥ 240 min of recording on at least one night. Quantitative diagnostic parameters were reviewed in a multidisciplinary team (MDT) meeting to formulate a management plan. Data are presented as mean (standard deviation), unless otherwise specified.</p><p><strong>Results: </strong>Seventeen people were screened, and 10 agreed to participate in the study (3F/7M). Eight participants (80%) successfully completed testing (2F/6M, 4 severe ID, age 29.7 [15.4] years, body mass index, BMI 27.1 [5.9] kg/m<sup>2</sup>, apnoea hypopnoea index, median AHI 5.5 [IQR 7.8] ev/h). Of these, five participants (63%) were found to have OSA. Feedback was favourable with an average total satisfaction score of 14.0 (4.8) out of 20 points.</p><p><strong>Conclusion: </strong>In a cohort of participants with ID who were unable to tolerate standard sleep diagnostics to assess OSA, an acoustic-derived home-based sleep study may provide a solution to achieve clinically diagnostic recordings.</p>","PeriodicalId":16163,"journal":{"name":"Journal of Intellectual Disability Research","volume":" ","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Acoustics-Derived Home-Based Sleep Study for the Diagnosis of Obstructive Sleep Apnoea in Adults With Intellectual Disabilities: A Feasibility Study.\",\"authors\":\"Lachlan Stranks, Mohammad Abdulsalam, David O'Regan, Joerg Steier, Alanna Hare\",\"doi\":\"10.1111/jir.70000\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Adults with intellectual disabilities (IDs) face significant health inequalities and reduced life expectancy compared to the general population. Sleep disorders, including obstructive sleep apnoea (OSA), are highly prevalent in this population; however, standard diagnostic modalities may be poorly tolerated and many people may remain undiagnosed. The aim of this study was to assess the feasibility of using an acoustic-derived home-based sleep study to diagnose OSA in adults with ID who were unable to tolerate standard inpatient or home sleep studies.</p><p><strong>Method: </strong>This was a prospective feasibility study (GSTT/2024/15803). Participants were identified from two tertiary outpatient sleep departments in London, UK. Eligible participants were aged ≥ 17 years with a diagnosed ID. Inpatient or existing home studies had not been tolerated or had been declined. Participants wore a small diagnostic sensor, the AcuPebble SA100 (Acurable Ltd., London, UK) for one to two nights in their own home. Baseline symptom screening and quality of life questionnaires were administered. Semiqualitative and qualitative feedback was obtained from participants. The primary outcome was successful completion of testing, defined as ≥ 240 min of recording on at least one night. Quantitative diagnostic parameters were reviewed in a multidisciplinary team (MDT) meeting to formulate a management plan. Data are presented as mean (standard deviation), unless otherwise specified.</p><p><strong>Results: </strong>Seventeen people were screened, and 10 agreed to participate in the study (3F/7M). Eight participants (80%) successfully completed testing (2F/6M, 4 severe ID, age 29.7 [15.4] years, body mass index, BMI 27.1 [5.9] kg/m<sup>2</sup>, apnoea hypopnoea index, median AHI 5.5 [IQR 7.8] ev/h). Of these, five participants (63%) were found to have OSA. Feedback was favourable with an average total satisfaction score of 14.0 (4.8) out of 20 points.</p><p><strong>Conclusion: </strong>In a cohort of participants with ID who were unable to tolerate standard sleep diagnostics to assess OSA, an acoustic-derived home-based sleep study may provide a solution to achieve clinically diagnostic recordings.</p>\",\"PeriodicalId\":16163,\"journal\":{\"name\":\"Journal of Intellectual Disability Research\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-06-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Intellectual Disability Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/jir.70000\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"EDUCATION, SPECIAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Intellectual Disability Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/jir.70000","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"EDUCATION, SPECIAL","Score":null,"Total":0}
Acoustics-Derived Home-Based Sleep Study for the Diagnosis of Obstructive Sleep Apnoea in Adults With Intellectual Disabilities: A Feasibility Study.
Background: Adults with intellectual disabilities (IDs) face significant health inequalities and reduced life expectancy compared to the general population. Sleep disorders, including obstructive sleep apnoea (OSA), are highly prevalent in this population; however, standard diagnostic modalities may be poorly tolerated and many people may remain undiagnosed. The aim of this study was to assess the feasibility of using an acoustic-derived home-based sleep study to diagnose OSA in adults with ID who were unable to tolerate standard inpatient or home sleep studies.
Method: This was a prospective feasibility study (GSTT/2024/15803). Participants were identified from two tertiary outpatient sleep departments in London, UK. Eligible participants were aged ≥ 17 years with a diagnosed ID. Inpatient or existing home studies had not been tolerated or had been declined. Participants wore a small diagnostic sensor, the AcuPebble SA100 (Acurable Ltd., London, UK) for one to two nights in their own home. Baseline symptom screening and quality of life questionnaires were administered. Semiqualitative and qualitative feedback was obtained from participants. The primary outcome was successful completion of testing, defined as ≥ 240 min of recording on at least one night. Quantitative diagnostic parameters were reviewed in a multidisciplinary team (MDT) meeting to formulate a management plan. Data are presented as mean (standard deviation), unless otherwise specified.
Results: Seventeen people were screened, and 10 agreed to participate in the study (3F/7M). Eight participants (80%) successfully completed testing (2F/6M, 4 severe ID, age 29.7 [15.4] years, body mass index, BMI 27.1 [5.9] kg/m2, apnoea hypopnoea index, median AHI 5.5 [IQR 7.8] ev/h). Of these, five participants (63%) were found to have OSA. Feedback was favourable with an average total satisfaction score of 14.0 (4.8) out of 20 points.
Conclusion: In a cohort of participants with ID who were unable to tolerate standard sleep diagnostics to assess OSA, an acoustic-derived home-based sleep study may provide a solution to achieve clinically diagnostic recordings.
期刊介绍:
The Journal of Intellectual Disability Research is devoted exclusively to the scientific study of intellectual disability and publishes papers reporting original observations in this field. The subject matter is broad and includes, but is not restricted to, findings from biological, educational, genetic, medical, psychiatric, psychological and sociological studies, and ethical, philosophical, and legal contributions that increase knowledge on the treatment and prevention of intellectual disability and of associated impairments and disabilities, and/or inform public policy and practice. Expert reviews on themes in which recent research has produced notable advances will be included. Such reviews will normally be by invitation.