Trajectories of Insomnia in Adults After Traumatic Brain Injury.
Trajectories of Insomnia in Adults After Traumatic Brain Injury.
复制标题
成年人创伤性脑损伤后的神经冲动轨迹。
DOI:
10.1001/jamanetworkopen.2021.45310
复制
发表时间:
2022-01-04
影响因子:
13.8
通讯作者:
Transforming Research and Clinical Knowledge in Traumatic Brain Injury (TRACK-TBI) Investigators
中科院分区:
文献类型:
--
作者:
Wickwire EM;Albrecht JS;Capaldi VF 2nd;Jain SO;Gardner RC;Werner JK;Mukherjee P;McKeon AB;Smith MT;Giacino JT;Nelson LD;Williams SG;Collen J;Sun X;Schnyer DM;Markowitz AJ;Manley GT;Krystal AD;Transforming Research and Clinical Knowledge in Traumatic Brain Injury (TRACK-TBI) Investigators
What is the natural history of insomnia in the 12 months after traumatic brain injury (TBI)? In this analysis of 2022 adults from the large cohort study Transforming Research and Clinical Knowledge in Traumatic Brain Injury, insomnia was common during the 12 months after TBI. Five trajectory classes of insomnia were identified, and baseline factors including sex, race and ethnicity, history of TBI, psychiatric history, and computed tomography status were identified as significantly associated with insomnia trajectory class membership. These findings suggest that insomnia is common after TBI and should be assessed early in recovery. This cohort study of 2022 adults with traumatic brain injury identifies unique trajectories of insomnia during the 12 months after injury based on serial assessment using standardized measures. Insomnia is common after traumatic brain injury (TBI) and contributes to morbidity and long-term sequelae. To identify unique trajectories of insomnia in the 12 months after TBI. In this prospective cohort study, latent class mixed models (LCMMs) were used to model insomnia trajectories over time and to classify participants into distinct profile groups. Data from the Transforming Research and Clinical Knowledge in Traumatic Brain Injury (TRACK-TBI) study, a longitudinal, multisite, observational study, were uploaded to the Federal Interagency Traumatic Brain Injury Repository (FITBIR) database. Participants were enrolled at 1 of 18 participating level I trauma centers and enrolled within 24 hours of TBI injury. Additional data were obtained directly from the TRACK-TBI investigators that will be uploaded to FITBIR in the future. Data were collected from February 26, 2014, to August 8, 2018, and analyzed from July 1, 2020, to November 15, 2021. Traumatic brain injury. Insomnia Severity Index assessed serially at 2 weeks and 3, 6, and 12 months thereafter. The final sample included 2022 participants (1377 [68.1%] men; mean [SD] age, 40.1 [17.2] years) from the FITBIR database and the TRACK-TBI study. The data were best fit by a 5-class LCMM. Of these participants, 1245 (61.6%) reported persistent mild insomnia symptoms (class 1); 627 (31.0%) initially reported mild insomnia symptoms that resolved over time (class 2); 91 (4.5%) reported persistent severe insomnia symptoms (class 3); 44 (2.2%) initially reported severe insomnia symptoms that resolved by 12 months (class 4); and 15 (0.7%) initially reported no insomnia symptoms but had severe symptoms by 12 months (class 5). In a multinomial logistic regression model, several factors significantly associated with insomnia trajectory class membership were identified, including female sex (odds ratio [OR], 1.65 [95% CI, 1.02-2.66]), Black race (OR, 2.36 [95% CI, 1.39-4.01]), history of psychiatric illness (OR, 2.21 [95% CI, 1.35-3.60]), and findings consistent with intracranial injury on computed tomography (OR, 0.36 [95% CI, 0.20-0.65]) when comparing class 3 with class 1. These results suggest important heterogeneity in the course of insomnia after TBI in adults. More work is needed to identify outcomes associated with these insomnia trajectory class subgroups and to identify optimal subgroup-specific treatment approaches.
登录
查看更多内容
影响因子:
4.8
作者:
Bastien, Celyne H.;Vallieres, Annie;Morin, Charles M.
通讯作者:
Morin, Charles M.
影响因子:
7.2
作者:
Strauss, Vicky Y.;Jones, Peter W.;Jordan, Kelvin P.
通讯作者:
Jordan, Kelvin P.
DOI:
10.1176/appi.ajp.2012.12040432
发表时间:
2013-04
期刊:
The American journal of psychiatry
影响因子:
--
作者:
Germain A
通讯作者:
Germain A
影响因子:
29
作者:
Nelson, Lindsay D.;Temkin, Nancy R.;Zafonte, Ross
通讯作者:
Zafonte, Ross
影响因子:
3
作者:
Taylor, Brent C.;Hagel, Emily M.;Sayer, Nina A.
通讯作者:
Sayer, Nina A.