医学
肌萎缩侧索硬化
强直性营养不良
机械通风
格林-巴利综合征
神经肌肉疾病
间歇强制通风
内科学
麻醉
心脏病学
免疫学
疾病
作者
Shinya Narukawa,Keita Ishizuka,Kohei Sugimoto,Kyoichi Nomura
摘要
Abstract Introduction/Aims Predicting when a patient will require invasive mechanical ventilation (IMV) is a major challenge in routine care for some neuromuscular diseases. In this study, we prospectively investigated whether phrenic nerve conduction studies (PNCS) can predict when IMV will be required in patients with amyotrophic lateral sclerosis (ALS), Guillain‐Barré syndrome (GBS), chronic inflammatory demyelinating polyneuropathy (CIDP), and myotonic dystrophy (DM). Methods PNCS amplitude (avAMP) and latency (avLAT) were compared between patients who required IMV (IMV group) and those who did not (non‐IMV group). PNCS were performed in 62 healthy controls and in patients with four different diseases that may require IMV: ALS (n = 56), GBS (n = 72), CIDP (n = 38), and DM (n = 24). Results The IMV group consisted of 12 patients with ALS, 14 with GBS, 2 with CIDP, and 4 with DM. avAMP was significantly lower in the IMV group with ALS than in the non‐IMV group ( P < .05), but no significant difference was observed in avLAT. avAMP was significantly lower and avLAT was significantly longer in the IMV group with GBS than in the non‐IMV group (both P < .05). Receiver operating characteristic analysis showed that the avAMP cutoff between the IMV and non‐IMV groups was 184.3 μV (area under the curve = 0.921; sensitivity, 84.6%; specificity, 88.2%) for ALS and GBS. Discussion PNCSs may aid in determining whether a patient with ALS or GBS requires IMV.
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