BioMarin (UK) Limited, London, UK.
Guy's and St Thomas' NHS Foundation Trust, London, UK.
Orphanet J Rare Dis. 2023 Jul 25;18(1):211. doi: 10.1186/s13023-023-02811-5.
The natural history of skeletal complications in achondroplasia (ACH) is well-described. However, it remains unclear how the rates of non-skeletal complications, surgical procedures, healthcare needs and mortality differ between individuals with ACH and the general population. This study aimed to contextualise the extent of these outcomes by comparing event rates across the lifespan, between those with ACH and matched controls in a United Kingdom (UK) population.
This retrospective, matched cohort study used data from national UK databases: the Clinical Practice Research Database (CPRD) GOLD from primary care, the secondary care Hospital Episode Statistics (HES) databases and the Office of National Statistics mortality records. ACH cases were identified using disorder-specific Read Codes or International Classification of Diseases 10th Revision codes. For each ACH case, up to four age- and sex-matched controls (defined as those without evidence of skeletal/growth disorders) were included. Event rates per 100 person-years were calculated for a pre-defined set of complications (informed by reviews of existing ACH literature and discussion with clinical authors), healthcare visits and mortality. Rate ratios (RRs) with 95% confidence intervals (CIs) were used to compare case and control cohorts.
541 ACH cases and 2052 controls were identified for the CPRD cohort; of these, 275 cases and 1064 matched controls had linkage to HES data. Approximately twice as many non-skeletal complications were reported among individuals with ACH versus controls (RR [95% CI] 1.80 [1.59-2.03]). Among ACH cases, a U-shaped distribution of complications was observed across age groups, whereby the highest complication rates occurred at < 11 and > 60 years of age. Individuals with ACH had greater needs for medication, GP referrals to specialist care, medical imaging, surgical procedures and healthcare visits versus controls, as well as a mortality rate of almost twice as high.
Patients with ACH experience high rates of a range of both skeletal and non-skeletal complications across their lifespan. To manage these complications, individuals with ACH have significantly increased healthcare needs compared to the general population. These results underscore the need for more coordinated and multidisciplinary management of people with ACH to improve health outcomes across the lifespan.
成骨不全症(ACH)骨骼并发症的自然病史已有详细描述。然而,ACH 患者与普通人群相比,非骨骼并发症、手术程序、医疗保健需求和死亡率的发生率差异仍不清楚。本研究旨在通过比较英国(UK)人群一生中的事件发生率,来了解这些结果的严重程度,ACH 患者与匹配对照组之间的发生率差异。
这是一项回顾性、匹配队列研究,使用了来自英国国家数据库的数据:初级保健的临床实践研究数据库(CPRD)GOLD、二级保健医院入院统计(HES)数据库和国家统计局死亡率记录。ACH 病例通过特定疾病的 Read 代码或国际疾病分类第 10 版代码来识别。对于每个 ACH 病例,纳入最多 4 名年龄和性别匹配的对照(定义为无骨骼/生长障碍证据者)。根据现有 ACH 文献综述和与临床作者的讨论,为一组预先定义的并发症(包括非骨骼并发症)、医疗就诊和死亡率计算每 100 人年的发生率。使用率比(RR)及其 95%置信区间(CI)比较病例和对照组。
CPRD 队列共确定了 541 例 ACH 病例和 2052 例对照;其中,275 例病例和 1064 例匹配对照与 HES 数据相关联。ACH 患者报告的非骨骼并发症数量几乎是对照组的两倍(RR [95%CI] 1.80 [1.59-2.03])。在 ACH 病例中,并发症的发生率随年龄组呈 U 型分布,即并发症发生率最高的年龄组为<11 岁和>60 岁。ACH 患者与对照组相比,药物治疗、全科医生向专科医生转诊、医学影像、手术程序和医疗就诊的需求更高,死亡率几乎高出一倍。
ACH 患者一生中会经历一系列骨骼和非骨骼并发症,发生率很高。为了管理这些并发症,ACH 患者的医疗保健需求明显高于普通人群。这些结果强调了需要更协调和多学科的管理,以改善 ACH 患者的健康结局。