Potential Role for Nocturnal PtcCO2 Monitoring in the Close Follow up of ALS Patients.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 66
- 试验地点
- 2
- 主要终点
- Nocturnal Transcutaneous PCO2
研究概览
简要总结
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease affecting motoneurons, with a prevalence around 5/100.000. Respiratory muscle involvement is a major feature in ALS and remains the main prognostic factor. Timing and rate of progression of this respiratory muscle involvement is also highly variable among individuals.
Respiratory manifestations justify a careful follow up including clinical evaluation, pulmonary function tests and blood gases. Prognostic value of respiratory muscle assessment has been clearly demonstrated in ALS, although several cut off values have been published. The clinical benefit of non invasive ventilation (NIV) is well established in ALS, but the optimal criteria for its initiation remain debated .
The 1999 consensus for NIV selected classical criteria to consider NIV in patients with respiratory symptoms suggesting hypoventilation: daytime hypercapnia (PaCO2 > 45 mmHg), nocturnal SaO2 < 89 % more than 5 consecutive minutes and for progressive neuromuscular disorders (NMD) (mainly ALS), a vital capacity (VC) < 50 % pred or a PImax < 60 cmH2O.
Besides daytime clinical and PFT assessment, nocturnal evaluation is essential in ALS. The prevalence of sleep apnea ranges from 16 % to 76 %.
Transcutaneous PCO2 (tcPCO2) is an attractive technique to evaluate non invasively nocturnal hypoventilation. The technique is well validated in different settings. Its use in neuromuscular disorders (NMD) is recent. In particular one study has demonstrated a high predictive value of tcPCO2 for the development of daytime hypoventilation within 1 year. To our knowledge, this technique has not been specifically assessed in ALS. There is a potential role for nocturnal PtcCO2 monitoring in the close follow up of ALS patients. Indeed, a close respiratory follow up of ALS patients is essential to determine the optimal timing of NIV, avoiding the occurence of unexpected acute respiratory failure.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Amyotrophic lateral sclerosis :definite, probable or probable with EMG (Airlie House Criteria, 1998).
- •Forced vital capacity >70% pred.
- •Daytime PaCO2 <43 mmHg.
- •Venous HCO3- <28 mmol/L
排除标准
- •Patients unable to perform pulmonary function tests or nocturnal recordings.
- •Coexisting significant lung disease: moderate to severe asthma or COPD
- •Current NIV, CPAP or oxygen therapy.
研究组 & 干预措施
PtcCO2
干预措施: PtcCO2 (Device)
结局指标
主要结局
Nocturnal Transcutaneous PCO2
时间窗: 6 months
次要结局
- Pulmonary function(6 months)
研究者
DELRIEU Jacqueline
PhD
Association Nationale pour les Traitements A Domicile, les Innovations et la Recherche
