Go Ronaldo C, Shah Roshan, Nyirenda Themba, Oe Yukiko, Sarfraz Khurram, Panthappattu Justin J, Philip Lesley, Bheeman Chandni, Shah Neel, Shah Sapan, Dar Sophia, Hung Sung, Rahman Waqas, Im Hyun, Marafelias Michael, Omidvari Karan, Pradhan Anuja, Sadikot Sean, Rose Keith M, Sperber Steven J, Josephs Joshua
Hackensack Meridian School of Medicine, Nutley, NJ.
Division of Pulmonary, Critical Care and Sleep Medicine, Hackensack University Medical Center, Hackensack, NJ.
Crit Care Explor. 2021 Jul 19;3(7):e0493. doi: 10.1097/CCE.0000000000000493. eCollection 2021 Jul.
To determine methylprednisolone's dose, duration, and administration from onset of symptoms and association with 60 days in hospital survival of coronavirus disease 2019 pneumonia.
Cohort study.
Thirteen hospitals in New Jersey, United States during March to June 2020.
Seven-hundred fifty-nine hospitalized coronavirus disease 2019 patients.
We performed a propensity matched cohort study between patients who received methylprednisolone and no methylprednisolone. Patients in the methylprednisolone group were further differentiated into dose (high dose and low dose), duration, and administration from onset of symptoms.
In the propensity matched sample, 99 out of 380 (26%) in no methylprednisolone, 69 out of 215 (31.9%) in low-dose methylprednisolone, and 74 out of 164 (55.2%) high-dose methylprednisolone expired. Overall median survival for no methylprednisolone (25.0 d), low-dose methylprednisolone (39.0 d), high-dose methylprednisolone (20.0 d), less than or equal to 7 days duration (19.0 d), 7-14 days duration (30.0 d), greater than 14 days duration (44.0 d), onset of symptoms less than or equal to 7 days (20.0 d), and onset of symptoms 7-14 days (27.0 d) were statistically significant (log-rank ≤ 0.001). Multivariate Cox regression showed nursing home residents, coronary artery disease, and invasive mechanical ventilation were independently associated with mortality. Methylprednisolone was associated with reduced mortality compared with no methylprednisolone (hazard ratio, 0.40; 95% CI, 0.27-0.59; < 0.001) but no added benefit with high dose. Low-dose methylprednisolone for 7-14 days was associated with reduced mortality compared with less than or equal to 7 days (hazard ratio, 0.45; 95% CI, 0.22-0.91; = 0.0273), and no additional benefit if greater than 14 days (hazard ratio, 1.27; 95% CI, 0.60-2.69; = 0.5434). Combination therapy with tocilizumab was associated with reduced mortality over monotherapy ( < 0.0116).
Low-dose methylprednisolone was associated with reduced mortality if given greater than 7 days from onset of symptoms, and no additional benefit greater than 14 days. High dose was associated with higher mortality.
确定甲基强的松龙的剂量、用药时长以及从症状出现开始的给药方式,及其与2019冠状病毒病肺炎患者60天住院生存率的关联。
队列研究。
2020年3月至6月期间美国新泽西州的13家医院。
759例住院的2019冠状病毒病患者。
我们对接受甲基强的松龙和未接受甲基强的松龙的患者进行了倾向匹配队列研究。甲基强的松龙组的患者进一步按剂量(高剂量和低剂量)、用药时长以及从症状出现开始的给药方式进行区分。
在倾向匹配样本中,未接受甲基强的松龙的380例患者中有99例(26%)死亡,低剂量甲基强的松龙组的215例患者中有69例(31.9%)死亡,高剂量甲基强的松龙组的164例患者中有74例(55.2%)死亡。未接受甲基强的松龙组(25.0天)、低剂量甲基强的松龙组(39.0天)、高剂量甲基强的松龙组(20.0天)、用药时长小于或等于7天组(19.0天)、7 - 14天组(30.0天)、大于14天组(44.0天)、症状出现小于或等于7天组(20.0天)以及症状出现7 - 14天组(27.0天)的总体中位生存期具有统计学意义(对数秩检验≤0.001)。多因素Cox回归显示,养老院居民、冠状动脉疾病和有创机械通气与死亡率独立相关。与未接受甲基强的松龙相比,甲基强的松龙与死亡率降低相关(风险比,0.40;95%置信区间,0.27 - 0.59;<0.001),但高剂量并无额外益处。与用药时长小于或等于7天相比,低剂量甲基强的松龙用药7 - 14天与死亡率降低相关(风险比,0.45;95%置信区间,0.22 - 0.91;=0.0273),用药大于14天则无额外益处(风险比,1.27;95%置信区间,0.60 - 2.69;=0.5434)。与单药治疗相比,托珠单抗联合治疗与死亡率降低相关(<0.0116)。
症状出现后大于7天给予低剂量甲基强的松龙与死亡率降低相关,大于14天则无额外益处。高剂量与更高死亡率相关。