Nater J P, Brain R G, Deutman R, Mulder T J
Contact Dermatitis. 1976 Oct;2(5):259-61. doi: 10.1111/j.1600-0536.1976.tb03044.x.
Sixty-six patients who had to undergo total hip replacement by means of a metal-to-plastic Stanmore prosthesis, were patch-tested prior to and 6 to 12 months after surgery with the standard ICDRG all allergens series and with acrylic monomer 5% in acetone. In 62 patients the history of metal allergy as well as the patch tests to all tested allergens were negative. One patient with a history of metal allergy reacted negatively before surgery; about 6 months after surgery the patch test to nickel sulphate was positive (2 plus). Three other patients developed positive patch test reaction after surgery: two reacted positively to nickel sulphate (2 plus) and one to cobalt chloride (2 plus). In none of the 66 patients have local side effects of the prostheses been found to date.
66例必须通过金属对塑料的斯坦莫尔假体进行全髋关节置换的患者,在手术前以及术后6至12个月,使用标准的国际接触性皮炎研究组(ICDRG)所有过敏原系列以及5%丙烯酸单体丙酮溶液进行了斑贴试验。62例患者的金属过敏史以及对所有测试过敏原的斑贴试验均为阴性。1例有金属过敏史的患者在手术前反应为阴性;术后约6个月,对硫酸镍的斑贴试验呈阳性(2级阳性)。另外3例患者术后出现阳性斑贴试验反应:2例对硫酸镍呈阳性反应(2级阳性),1例对氯化钴呈阳性反应(2级阳性)。迄今为止,66例患者中均未发现假体的局部副作用。