Kelsey E. Joyce, Kimberly Ashdown, John P. Delamere, Chris Bradley, Christopher T. Lewis, Abigail Letchford, Rebekah A. I. Lucas, Will Malein, Owen Thomas, Arthur R. Bradwell, Samuel J. E. Lucas
{"title":"Nocturnal pulse oximetry for the detection and prediction of acute mountain sickness: An observational study","authors":"Kelsey E. Joyce, Kimberly Ashdown, John P. Delamere, Chris Bradley, Christopher T. Lewis, Abigail Letchford, Rebekah A. I. Lucas, Will Malein, Owen Thomas, Arthur R. Bradwell, Samuel J. E. Lucas","doi":"10.1113/EP091691","DOIUrl":null,"url":null,"abstract":"<p>Acute mountain sickness (AMS) is a well-studied illness defined by clinical features (e.g., headache and nausea), as assessed by the Lake Louise score (LLS). Although obvious in its severe form, early stages of AMS are poorly defined and easily confused with common travel-related conditions. Measurement of hypoxaemia, the cause of AMS, should be helpful, yet to date its utility for identifying AMS susceptibility remains unclear. This study quantified altitude-induced hypoxaemia in individuals during an ascent to 4800 m to determine the utility of nocturnal pulse oximetry measurements for prediction of AMS. Eighteen individuals (36 ± 16 years of age) ascended to 4800 m over 12 days. Symptomology of AMS was assessed each morning via LLS criteria, with participants categorized as either AMS-positive (LLS ≥ 3 with headache) or AMS-negative. Overnight peripheral oxygen saturations (ov-<span></span><math>\n <semantics>\n <msub>\n <mi>S</mi>\n <mrow>\n <mi>p</mi>\n <msub>\n <mi>O</mi>\n <mn>2</mn>\n </msub>\n </mrow>\n </msub>\n <annotation>${{S}_{{\\mathrm{p}}{{{\\mathrm{O}}}_2}}}$</annotation>\n </semantics></math>) were recorded continuously (1 Hz) using portable oximeters. Derivatives of these recordings were compared between AMS-positive and -negative subjects (Mann–Whitney <i>U</i>-test). Exploratory analyses (Pearson's) were conducted to investigate relationships between overnight parameters and AMS severity. Overnight derivatives, including ov-<span></span><math>\n <semantics>\n <msub>\n <mi>S</mi>\n <mrow>\n <mi>p</mi>\n <msub>\n <mi>O</mi>\n <mn>2</mn>\n </msub>\n </mrow>\n </msub>\n <annotation>${{S}_{{\\mathrm{p}}{{{\\mathrm{O}}}_2}}}$</annotation>\n </semantics></math>, heart rate/ov-<span></span><math>\n <semantics>\n <msub>\n <mi>S</mi>\n <mrow>\n <mi>p</mi>\n <msub>\n <mi>O</mi>\n <mn>2</mn>\n </msub>\n </mrow>\n </msub>\n <annotation>${{S}_{{\\mathrm{p}}{{{\\mathrm{O}}}_2}}}$</annotation>\n </semantics></math>, variance, oxygen desaturation index, hypoxic burden and total sleep time at <80% <span></span><math>\n <semantics>\n <msub>\n <mi>S</mi>\n <mrow>\n <mi>p</mi>\n <msub>\n <mi>O</mi>\n <mn>2</mn>\n </msub>\n </mrow>\n </msub>\n <annotation>${{S}_{{\\mathrm{p}}{{{\\mathrm{O}}}_2}}}$</annotation>\n </semantics></math>, all differed significantly between AMS-positive and -negative subjects (all <i>P </i>< 0.01), with cumulative/relative frequency plots highlighting these differences visually. Exploratory analysis revealed that ov-<span></span><math>\n <semantics>\n <msub>\n <mi>S</mi>\n <mrow>\n <mi>p</mi>\n <msub>\n <mi>O</mi>\n <mn>2</mn>\n </msub>\n </mrow>\n </msub>\n <annotation>${{S}_{{\\mathrm{p}}{{{\\mathrm{O}}}_2}}}$</annotation>\n </semantics></math> from 3850 m was correlated with peak LLS at 4800 m (<i>r</i> = 0.58–0.61). The findings highlight the potential for overnight oximetry to predict AMS susceptibility during ascent to high altitude. Further investigation is required to develop, evaluate and optimize predictive models to improve AMS management and prevention.</p>","PeriodicalId":12092,"journal":{"name":"Experimental Physiology","volume":"109 11","pages":"1856-1868"},"PeriodicalIF":2.6000,"publicationDate":"2024-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1113/EP091691","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental Physiology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1113/EP091691","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Acute mountain sickness (AMS) is a well-studied illness defined by clinical features (e.g., headache and nausea), as assessed by the Lake Louise score (LLS). Although obvious in its severe form, early stages of AMS are poorly defined and easily confused with common travel-related conditions. Measurement of hypoxaemia, the cause of AMS, should be helpful, yet to date its utility for identifying AMS susceptibility remains unclear. This study quantified altitude-induced hypoxaemia in individuals during an ascent to 4800 m to determine the utility of nocturnal pulse oximetry measurements for prediction of AMS. Eighteen individuals (36 ± 16 years of age) ascended to 4800 m over 12 days. Symptomology of AMS was assessed each morning via LLS criteria, with participants categorized as either AMS-positive (LLS ≥ 3 with headache) or AMS-negative. Overnight peripheral oxygen saturations (ov-) were recorded continuously (1 Hz) using portable oximeters. Derivatives of these recordings were compared between AMS-positive and -negative subjects (Mann–Whitney U-test). Exploratory analyses (Pearson's) were conducted to investigate relationships between overnight parameters and AMS severity. Overnight derivatives, including ov-, heart rate/ov-, variance, oxygen desaturation index, hypoxic burden and total sleep time at <80% , all differed significantly between AMS-positive and -negative subjects (all P < 0.01), with cumulative/relative frequency plots highlighting these differences visually. Exploratory analysis revealed that ov- from 3850 m was correlated with peak LLS at 4800 m (r = 0.58–0.61). The findings highlight the potential for overnight oximetry to predict AMS susceptibility during ascent to high altitude. Further investigation is required to develop, evaluate and optimize predictive models to improve AMS management and prevention.
急性高山反应(AMS)是一种经过深入研究的疾病,其临床特征(如头痛和恶心)可通过路易斯湖评分(LLS)进行评估。虽然高山反应的严重程度显而易见,但其早期阶段的定义并不明确,很容易与常见的旅行相关疾病混淆。低氧血症是引起高山反应的原因,因此测量低氧血症应该会有所帮助,但迄今为止,低氧血症在确定高山反应易感性方面的作用仍不明确。本研究量化了个人在上升到海拔 4800 米时由海拔引起的低氧血症,以确定夜间脉搏血氧仪测量值对预测高山反应的实用性。18 人(36 ± 16 岁)在 12 天内登上了海拔 4800 米的高山。每天早上通过 LLS 标准评估 AMS 症状,并将参与者分为 AMS 阳性(LLS ≥ 3 且伴有头痛)或 AMS 阴性。使用便携式血氧仪连续(1 Hz)记录隔夜外周血氧饱和度(ov- S p O 2 ${{S}_{\{mathrm{p}}{{{\{mathrm{O}}}_2}}$ )。这些记录的衍生物在 AMS 阳性和阴性受试者之间进行比较(曼-惠特尼 U 检验)。进行了探索性分析(Pearson's),以研究隔夜参数与 AMS 严重程度之间的关系。隔夜衍生物包括ov- S p O 2 ${{S}_{\mathrm{p}}{{{\mathrm{O}}}_2}}$ 、心率/ov- S p O 2 ${{S}_{{\mathrm{p}}{{{\mathrm{O}}}}_2}}$ 、方差、氧饱和度指数、S p O 2 ${{S}_{\mathrm{p}}{{{mathrm{O}}}_2}}$ 时的缺氧负担和总睡眠时间,在 AMS 阳性和阴性受试者之间均存在显著差异(3850 米处的所有 P S p O 2 ${{S}_{\mathrm{p}}{{{\mathrm{O}}}_2}}$ 与 4800 米处的 LLS 峰值相关(r = 0.58-0.61).这些研究结果突显了夜间血氧仪在预测高海拔上升过程中 AMS 易感性方面的潜力。需要进行进一步调查,以开发、评估和优化预测模型,从而改善 AMS 的管理和预防。
期刊介绍:
Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged.
Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.