Ghassemi Jahani Shadi A, Danielson Barbro, Karlsson Jón, Danielsson Aina J
Department of Orthopaedics, Sahlgrenska University Hospital, Gothenburg, Sweden,
J Child Orthop. 2014 Oct;8(5):423-33. doi: 10.1007/s11832-014-0609-9. Epub 2014 Oct 10.
Between 1959 and 1962, several children with multiple malformations were born after maternal intake of thalidomide during pregnancy, known as thalidomide embryopathy (TE).
The aim of this study was to evaluate the malformations, their long-term effect on the function of the extremities and the development of degenerative osteoarthritis (OA) in the lower extremities.
All living persons with TE in Sweden were invited to participate in the study. Thirty-one patients were examined clinically as a part of a multi-disciplinary follow-up programme. Evaluation of upper and lower limb function was performed by validated questionnaires [Disabilities of the Arm, Shoulder and Hand (DASH) and Rheumatoid and Arthritis Outcome Score (RAOS), respectively] and radiographic appearance of lower limbs by the use of spiral computed tomography.
Five individuals had severe malformations of the lower limbs and proximal femoral focal deficiency (PFFD), with significantly reduced function as found on the RAOS values. Twenty-seven patients had two fully functional arms and hands, despite the fact that 8% of shoulders, 26% of elbows/forearms and 70% of hands were malformed. Loss of gripping function did not significantly affect the upper extremity function, as measured by the DASH score. Ten patients without major deformities had OA in the hips and 15 in the knees, mostly mild and with no effect on the RAOS value.
A wide variety of malformations in the upper and lower limbs was found in the study group. Degenerative changes were found in the hips and the knees but were mostly mild and without major clinical significance. Despite upper limb anomalies that affected the fine motor skills, upper extremity function was not significantly reduced for most individuals. Individuals with PFFD along with major deformities of upper limbs had a reduced function of upper as well as lower limbs.
1959年至1962年期间,数名母亲在孕期服用沙利度胺后生下了患有多种畸形的儿童,即所谓的沙利度胺胚胎病(TE)。
本研究旨在评估畸形情况、其对四肢功能的长期影响以及下肢退行性骨关节炎(OA)的发展。
邀请瑞典所有在世的TE患者参与本研究。作为多学科随访计划的一部分,对31名患者进行了临床检查。通过经过验证的问卷[分别为上肢、肩部和手部功能障碍量表(DASH)以及类风湿性关节炎和关节炎结局评分(RAOS)]评估上肢和下肢功能,并使用螺旋计算机断层扫描评估下肢的影像学表现。
5名个体存在严重的下肢畸形和近端股骨局灶性缺损(PFFD),RAOS值显示其功能显著降低。27名患者的双臂和双手功能完全正常,尽管8%的肩部、26%的肘部/前臂和70%的手部存在畸形。根据DASH评分,抓握功能丧失并未显著影响上肢功能。10名无重大畸形的患者髋关节患有OA,15名患者膝关节患有OA,大多为轻度,对RAOS值无影响。
研究组中发现了上肢和下肢的多种畸形。在髋关节和膝关节发现了退行性改变,但大多为轻度,无重大临床意义。尽管上肢异常影响了精细运动技能,但大多数个体的上肢功能并未显著降低。患有PFFD以及上肢重大畸形的个体上肢和下肢功能均有所降低。