Hewitt L Arthur, Lindsten Annika, Gorny Stephen, Karnik-Henry Meghana, Kymes Steven, Favit Antonella
Lundbeck Deerfield Illinois.
Lundbeck A/S Copenhagen Denmark.
Health Sci Rep. 2021 Jan 20;4(1):e227. doi: 10.1002/hsr2.227. eCollection 2021 Mar.
Patients with neurogenic orthostatic hypotension (nOH) due to autonomic dysfunction may also experience supine hypertension (defined as supine systolic blood pressure [SBP] ≥140 mmHg). Because pressor agents used to improve nOH symptoms by increasing standing blood pressure (BP) may exacerbate or cause supine hypertension, changes in supine BP with nOH treatments are of interest.
This post hoc study examined changes in SBP in patients receiving droxidopa (100-600 mg, three times daily) during a 12-month long-term extension study based on whether patients had supine hypertension (ie, supine SBP ≥140 mmHg) at baseline. Shifts from baseline in supine hypertension categorization and mean supine and standing SBP after 6 and 12 months of treatment with droxidopa were determined.
At baseline, 64 patients did not have supine hypertension (mean supine SBP, 120 mmHg) and 38 patients had supine hypertension (mean supine SBP, 157 mmHg). A similar percentage of patients shifted from their respective baseline supine hypertension categorization (ie, with or without supine hypertension) to the other category after receiving droxidopa for 6 or 12 months. After 12 months of droxidopa treatment, patients with supine hypertension at baseline had a mean supine SBP decrease of 3 mmHg and a mean standing SBP increase of 9 mmHg. Patients without supine hypertension at baseline had mean supine and standing SBP increases of 12 and 15 mmHg, respectively.
There was no consistent or progressive elevation in supine SBP over time during the 12-month treatment with droxidopa in patients either with or without supine hypertension at baseline. These data suggest that long-term droxidopa treatment for nOH does not adversely affect supine BP.
因自主神经功能障碍导致神经源性直立性低血压(nOH)的患者也可能出现卧位高血压(定义为卧位收缩压[SBP]≥140mmHg)。由于用于通过提高站立血压(BP)来改善nOH症状的升压药可能会加重或导致卧位高血压,因此nOH治疗期间卧位BP的变化备受关注。
这项事后分析研究在一项为期12个月的长期扩展研究中,根据患者基线时是否存在卧位高血压(即卧位SBP≥140mmHg),检查接受屈昔多巴(100 - 600mg,每日三次)治疗的患者SBP的变化。确定屈昔多巴治疗6个月和12个月后,卧位高血压分类从基线的变化以及平均卧位和站立位SBP。
基线时,64例患者没有卧位高血压(平均卧位SBP,120mmHg),38例患者有卧位高血压(平均卧位SBP,157mmHg)。接受屈昔多巴治疗6个月或12个月后,从各自基线卧位高血压分类(即有或无卧位高血压)转变为另一分类的患者比例相似。屈昔多巴治疗12个月后,基线时有卧位高血压的患者平均卧位SBP下降3mmHg,平均站立位SBP升高9mmHg。基线时无卧位高血压的患者平均卧位和站立位SBP分别升高12mmHg和15mmHg。
在为期12个月的屈昔多巴治疗期间,无论基线时有无卧位高血压,患者的卧位SBP均未随时间持续或逐渐升高。这些数据表明,长期使用屈昔多巴治疗nOH对卧位BP没有不利影响。