Krasuska-Sławińska Ewa, Brożyna Agnieszka, Dembowska-Bagińska Bożenna, Olczak-Kowalczyk Dorota
The Children's Memorial Health Institute, Warsaw, Poland.
Department of Pediatric Dentistry, Warsaw Medical University, Warsaw, Poland.
Contemp Oncol (Pozn). 2016;20(1):45-51. doi: 10.5114/wo.2015.55319. Epub 2016 Mar 16.
To determine reasons for the increase in caries among children/adolescents treated for neoplasms.
Health promoting behaviour, oral hygiene (PLI), gingiva (GI), dentition (DMFt/DMFs), number of teeth with white spot lesions (WSL), and enamel defects (ED) were assessed in three groups of 60 patients each. The three groups were as follows: under chemotherapy (CH), after chemotherapy (PCH), and generally healthy (CG). Medical files supplied information on neoplasm type, chemotherapeutic type and dose, age at treatment start, chemotherapy duration, and complications. Statistical analysis was performed with Mann-Whitney U test and Spearman's rho test.
The age at which chemotherapy was started/its duration was 5.9 ±4.0/1.3 ±0.5 years in PCH and 9.12 ±4.44/0.8 ±0.3 years in CH; PCH completed treatment 4.9 ±3.4 years ago. Chemotherapy most often included vincristine (VCR), etoposide (VP-16), adriamycin (ADM), cyclophosphamide (CTX), cisplatin (CDDP), and ifosphamide (IF). Mucositis occurrence was 28.33% in PCH and 45.00% in CH; vomiting occurrence was 43.33% and 50.00%, respectively. Nutrition and prophylaxis mistakes occurred more often in CH/PCH than in CG; PLI, GI, caries incidence and severity, and the number of teeth with WSL were higher. Correlation between caries incidence and chemotherapeutic type and dose, age at treatment start and treatment duration, mucositis, emesis, PLI, GI, ED, no fluoride prophylaxis, and nutritional mistakes was established. Ifosphamide and mucositis treatment played a major role in chemotherapy; after chemotherapy - ED and CTX, ADM, IF, and VP-16.
Caries in permanent teeth in children/adolescents undergoing chemotherapy result from nutritional mistakes, poor prophylaxis, and indirectly from chemotherapy complications (first mucositis and emesis, and later developmental ED).
确定接受肿瘤治疗的儿童/青少年龋齿增加的原因。
对三组各60例患者的健康促进行为、口腔卫生(菌斑指数,PLI)、牙龈(牙龈指数,GI)、牙列(恒牙龋失补牙数,DMFt/乳牙龋失补牙数,DMFs)、出现白斑病变(WSL)的牙齿数量以及釉质缺陷(ED)进行评估。三组如下:化疗中(CH)、化疗后(PCH)和一般健康组(CG)。病历提供了肿瘤类型、化疗类型和剂量、开始治疗时的年龄、化疗持续时间以及并发症的信息。采用曼-惠特尼U检验和斯皮尔曼等级相关检验进行统计分析。
PCH组开始化疗的年龄/化疗持续时间为5.9±4.0/1.3±0.5岁,CH组为9.12±4.44/0.8±0.3岁;PCH组在4.9±3.4年前完成治疗。化疗最常使用长春新碱(VCR)、依托泊苷(VP-16)、阿霉素(ADM)、环磷酰胺(CTX)、顺铂(CDDP)和异环磷酰胺(IF)。PCH组黏膜炎发生率为28.33%,CH组为45.00%;呕吐发生率分别为43.33%和50.00%。CH/PCH组比CG组更常出现营养和预防方面的失误;PLI、GI、龋齿发生率和严重程度以及出现WSL的牙齿数量更高。确定了龋齿发生率与化疗类型和剂量、开始治疗时的年龄和治疗持续时间、黏膜炎、呕吐、PLI、GI、ED、未进行氟化物预防以及营养失误之间的相关性。异环磷酰胺和黏膜炎治疗在化疗中起主要作用;化疗后则是ED以及CTX、ADM、IF和VP-16起主要作用。
接受化疗的儿童/青少年恒牙龋齿是由营养失误、预防措施不力以及化疗并发症(首先是黏膜炎和呕吐,随后是发育性ED)间接导致的。