American Porphyria Foundation, 4915 St. Elmo Avenue, Suite 200, Bethesda, MD, USA.
British Porphyria Association, Durham, UK.
Adv Ther. 2022 Sep;39(9):4330-4345. doi: 10.1007/s12325-022-02172-8. Epub 2022 Jul 30.
Acute hepatic porphyria (AHP) is a family of rare metabolic diseases characterized by potentially life-threatening acute attacks and, in some patients, chronic debilitating symptoms. While patients with frequent or recurrent attacks (three or more attacks annually) are known to have reduced health-related quality of life (HRQoL) as most aspects of daily living are impacted, limited data exist in patients with sporadic attacks. This research aims to identify porphyria-related symptoms between attacks, characterize the frequency, severity, and bothersomeness of these symptoms, and more generally understand the burden of this disease in patients who experience attacks sporadically.
Patients with AHP with sporadic attacks (AHP-SA) (at least one porphyria attack in the past 2 years, but no more than two attacks per year in the previous 2 years) were recruited, via outreach performed by patient advocacy groups, for participation in qualitative telephone interviews. Interviews were conducted using a semi-structured guide and were audio-recorded, transcribed, anonymized, coded, and analyzed to determine if saturation was reached.
A total of 14 participants with AHP-SA were interviewed (mean age 45 years, 100% female). The most frequently reported chronic symptoms were fatigue, pain, heartburn, and constipation. The most frequently experienced chronic impacts were difficulty performing daily activities, difficulty exercising, negative impact on work, need for a special diet, anxiety, and depression. Beyond these chronic symptoms and impacts, participants also frequently described flares in their porphyria that were severe, did not qualify in their minds as an acute attack, but were nonetheless more severe than their typical chronic experience.
Patients with acute hepatic porphyria who experience sporadic attacks face significant chronic symptoms and impacts that frequently require significant pharmacological and clinical treatment. The reported severity of these symptoms and impacts suggests that the humanistic burden of AHP-SA is substantial and may lead to a significant decrease in health-related quality of life in these patients between acute attacks. The presence of flares that do not reach the level of what is considered an acute attack by patients is a unique finding of this study not reported elsewhere and requires additional investigation.
急性肝性卟啉症(AHP)是一组罕见的代谢疾病,其特征为潜在危及生命的急性发作,且部分患者会出现慢性虚弱症状。虽然已知频繁或反复发作(每年发作 3 次或以上)的患者健康相关生活质量(HRQoL)会降低,因为日常生活的各个方面都受到影响,但在偶发性发作的患者中,此类数据有限。本研究旨在确定发作间期的卟啉症相关症状,描述这些症状的频率、严重程度和困扰程度,并更全面地了解偶发性发作患者的疾病负担。
通过患者权益倡导团体开展外联活动,招募了过去 2 年内有过至少 1 次、过去 2 年内每年不超过 2 次发作的 AHP 偶发性发作(AHP-SA)患者参与定性电话访谈。访谈采用半结构化指南进行,并进行音频记录、转录、匿名、编码和分析,以确定是否达到饱和。
共对 14 名 AHP-SA 患者进行了访谈(平均年龄 45 岁,100%为女性)。报告最频繁的慢性症状为疲劳、疼痛、胃灼热和便秘。报告最频繁的慢性影响为日常活动困难、运动困难、工作受影响、需要特殊饮食、焦虑和抑郁。除了这些慢性症状和影响外,患者还经常描述他们的卟啉症发作,这些发作非常严重,在他们看来不符合急性发作的标准,但仍比他们典型的慢性发作更严重。
偶发性发作的急性肝性卟啉症患者面临着严重的慢性症状和影响,这些症状和影响通常需要进行大量的药物和临床治疗。这些症状和影响的严重程度表明,AHP-SA 的人文负担很大,可能会导致这些患者在急性发作之间的健康相关生活质量显著下降。患者报告的不符合急性发作标准的发作的存在是本研究的一个独特发现,尚未在其他地方报道,需要进一步调查。