Professor and Head of Unit.
Senior Resident Doctor.
J Assoc Physicians India. 2023 Aug;71(8):11-12. doi: 10.59556/japi.71.0286.
Hemophilia is an X-linked recessive inherited disease affecting the coagulation pathway due to congenital deficiencies in either factor VIII (hemophilia A) or factor IX (hemophilia B). The clinical assessment of a patient's functional ability and the state of joint conditions is carried out by the clinicians by administering questionnaires namely the Gilbert or the World Federation of Hemophilia Physical Examination (WFH-PE) score for joint condition and Functional Independence Score in Hemophilia (FISH) for joint function. Here, we have studied the clinical profile of adult hemophilia patients with the short- and long-term complications of the disease. Additionally, the FISH score and the Gilbert score are calculated to assess functional independence and joint condition, respectively. The scores were also compared according to the severity of the disease.
An observational cross-sectional study of 40 adult hemophilia patients was carried out in Sir Sayajirao General Hospital and Medical College, Baroda, Gujarat, India, over a period of 1 year. Data regarding age, sex, and complications associated with the disease were collected in the form of a questionnaire. The overall mean and standard deviation (SD) of FISH and Gilbert scores were calculated and correlated with the severity of the disease.
The majority of cases (19) were between 20 and 40 years, and most (24) were diagnosed in childhood. All the subjects were male and all except one had hemophilia A. Family history was seen in only half of the cases. Nine had mild, 20 had moderate, and 11 had severe disease. Around 46% of the subjects had joint arthropathy with the knee joint most affected (60%) followed by the ankle (22.5%). The mean FISH score was 27.132 ± 4.0691 with a minimum score of 15 in severe disease suggesting more functional deficit. The average Gilbert score was 7.4 ± 2.985 with a maximum score of 14 in severe disease suggesting more joint damage Interpretations and conclusion: All subjects were male and except one all had hemophilia A. Majority were between 20 and 40 years but most were diagnosed before 10 years of age and only 50% had positive family history. Arthropathy is the most common complication with the knee joint being most affected. Majority of mild hemophiliacs achieved a maximum FISH score denoting maximum functional capacity. Compared to existing studies, our study showed better FISH scores in moderate hemophiliacs suggesting more functional independence. While comparing Gilbert's score to other studies, moderate and severe hemophiliacs in our study showed less joint damage.
血友病是一种 X 连锁隐性遗传性疾病,由于先天性因子 VIII(血友病 A)或因子 IX(血友病 B)缺乏,导致凝血途径异常。临床医生通过评估患者的功能能力和关节状况,采用吉尔伯特或世界血友病联合会体格检查(WFH-PE)评分评估关节状况和血友病的功能独立性评分(FISH)评估关节功能。在这里,我们研究了成年血友病患者的临床特征及其疾病的短期和长期并发症。此外,还计算了 FISH 评分和吉尔伯特评分,分别评估功能独立性和关节状况。根据疾病的严重程度对评分进行了比较。
在印度古吉拉特邦巴罗达的萨亚杰拉奥总医院和医学院进行了一项为期 1 年的 40 名成年血友病患者的观察性横断面研究。以问卷形式收集了年龄、性别和与疾病相关的并发症等数据。计算了 FISH 和吉尔伯特评分的总体平均值和标准差(SD),并与疾病的严重程度相关联。
大多数患者(19 例)年龄在 20 至 40 岁之间,大多数(24 例)在儿童时期被诊断出患有该疾病。所有患者均为男性,除 1 例外均患有血友病 A。仅一半的病例有家族史。9 例为轻度,20 例为中度,11 例为重度。约 46%的患者有关节关节炎,最受影响的关节是膝关节(60%),其次是踝关节(22.5%)。FISH 评分的平均值为 27.132 ± 4.0691,重度疾病的最低评分为 15,提示功能缺陷更大。平均吉尔伯特评分为 7.4 ± 2.985,重度疾病的最高评分为 14,提示关节损伤更大。
所有患者均为男性,除 1 例外均为血友病 A。大多数患者年龄在 20 至 40 岁之间,但大多数患者在 10 岁之前被诊断出患有该疾病,仅有 50%有阳性家族史。关节炎是最常见的并发症,最受影响的关节是膝关节。大多数轻度血友病患者的 FISH 评分最高,提示功能能力最大。与现有研究相比,我们的研究显示中度血友病患者的 FISH 评分更好,提示功能独立性更高。与其他研究相比,我们研究中的中度和重度血友病患者的吉尔伯特评分显示关节损伤较小。