Kim Byung-Su, Chung Pil-Wook, Kim Byung-Kun, Lee Mi Ji, Chu Min Kyung, Ahn Jin-Young, Bae Dae Woong, Song Tae-Jin, Sohn Jong-Hee, Oh Kyungmi, Kim Daeyoung, Kim Jae-Moon, Park Jeong Wook, Chung Jae Myun, Moon Heui-Soo, Cho Soohyun, Seo Jong-Geun, Kim Soo-Kyoung, Choi Yun-Ju, Park Kwang-Yeol, Chung Chin-Sang, Cho Soo-Jin
Department of Neurology, Daejin Medical Center, Bundang Jesaeng General Hospital, Seongnam, South Korea.
Department of Neurology, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Front Neurol. 2022 Feb 10;13:827734. doi: 10.3389/fneur.2022.827734. eCollection 2022.
Cluster headache (CH) is a rare, primary headache disorder, characterized of excruciating, strictly one-sided pain attacks and ipsilateral cranial autonomic symptoms. Given the debilitating nature of CH, delayed diagnosis can increase the disease burden. Thus, we aimed to investigate the diagnostic delay, its predictors, and clinical influence among patients with CH.
Data from a prospective multicenter CH registry over a 4-year period were analyzed. CH was diagnosed according to the International Classification of Headache Disorders (ICHD)-3 criteria, and diagnostic delay of CH was assessed as the time interval between the year of the first onset and the year of CH diagnosis. Patients were classified into three groups according to the tertiles of diagnostic delay (1st tertile, <1 year; 2nd tertile, 1-6 years; and 3rd tertile, ≥7 years).
Overall, 445 patients were evaluated. The mean duration of diagnosis delay was 5.7 ± 6.7 years, (range, 0-36 years). Regarding the age of onset, majority of young patients (age <20 years) belonged to the third tertile (60%), whereas minority of old patients (>40 years) belonged to the third tertile (9.0%). For year of onset, the proportion of patients in the 3rd tertile was the highest for the groups before the publication year of the ICHD-2 (74.7%) and the lowest for the groups after the publication year of the ICHD-3 beta version (0.5%). Compared with the first CH, episodic CH [multivariable-adjusted odds ratio (aOR) = 5.91, 95% CI = 2.42-14.48], chronic CH (aOR = 8.87, 95% CI = 2.66-29.51), and probable CH (aOR = 4.12, 95% CI = 1.48-11.43) were associated with the tertiles of diagnostic delay. Age of onset (aOR = 0.97, 95% CI = 0.95-0.99) and PHQ-9 score (aOR = 0.96, 95% CI = 0.93-0.99) were inversely associated with the tertile of diagnostic delay. The prevalence of suicidal ideation was highest in the patients of the third tertile. The mean HIT-6 score increased significantly with the diagnostic delay ( = 0.041).
Patients with a younger onset of CH have a higher risk of diagnostic delay. Nevertheless, the rate of delayed diagnosis gradually improved over time and with the publication of the ICHD criteria, supporting the clinical significance of diagnostic clinical criteria and headache education to reduce the disease burden of CH.
丛集性头痛(CH)是一种罕见的原发性头痛疾病,其特征为剧烈的、严格单侧的疼痛发作以及同侧颅神经自主症状。鉴于CH的致残性,诊断延迟会增加疾病负担。因此,我们旨在调查CH患者的诊断延迟情况、其预测因素及临床影响。
分析了一个前瞻性多中心CH登记处4年期间的数据。CH根据国际头痛疾病分类(ICHD)-3标准进行诊断,CH的诊断延迟被评估为首次发病年份与CH诊断年份之间的时间间隔。根据诊断延迟的三分位数将患者分为三组(第一三分位数,<1年;第二三分位数,1 - 6年;第三三分位数,≥7年)。
总体上,评估了445例患者。诊断延迟的平均时长为5.7±6.7年(范围,0 - 36年)。关于发病年龄,大多数年轻患者(年龄<20岁)属于第三三分位数(60%),而老年患者(>40岁)中少数属于第三三分位数(9.0%)。对于发病年份,ICHD - 2出版年份之前的组中第三三分位数的患者比例最高(74.7%),而ICHD - 3β版出版年份之后的组中该比例最低(0.5%)。与首次CH相比,发作性CH[多变量调整优势比(aOR)= 5.91,95%置信区间(CI)= 2.42 - 14.48]、慢性CH(aOR = 8.87,95% CI = 2.66 - 29.51)和可能的CH(aOR = 4.12,95% CI = 1.48 - 11.43)与诊断延迟的三分位数相关。发病年龄(aOR = 0.97,95% CI = 0.95 - 0.99)和PHQ - 9评分(aOR = 0.96,95% CI = 0.93 - 0.99)与诊断延迟的三分位数呈负相关。自杀意念的患病率在第三三分位数的患者中最高。平均HIT - 6评分随诊断延迟显著增加(P = 0.041)。
CH发病年龄较小的患者诊断延迟风险较高。然而,随着时间推移以及ICHD标准的发布,延迟诊断率逐渐改善,这支持了诊断临床标准和头痛教育对减轻CH疾病负担的临床意义。