Dental Pulp Therapy for Primary Teeth in Children Undergoing Cancer Therapy

被引:8
|
作者
Halperson, Elinor [1 ]
Moss, Dinna [1 ]
Tickotsky, Nili [2 ]
Weintraub, Michael [3 ]
Moskovitz, Moti [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Sch Dent Med, Dept Pediat Dent, Jerusalem, Israel
[2] Bar Ilan Univ, Ramat Gan, Israel
[3] Hadassah Hebrew Univ, Med Ctr, Dept Pediat Hematol Oncol & Bone Marrow Transplan, Jerusalem, Israel
关键词
childhood cancer; dental care; pulpotomy; MANAGEMENT; RADIATION; PULPOTOMY;
D O I
10.1002/pbc.25227
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundChildhood cancer treatment negatively affects the immune system, increasing the risk for bacteremia and septicemia. As the oral cavity is a major entry portal for pathogens into the bloodstream dental care in such children tends to be radical, favouring tooth extraction over less drastic treatments such as pulpotomy, the amputation of infected dental pulp. The present study aimed to compare pulpotomy treatment success rate in children with cancer receiving immunosuppressive therapy with that of healthy children, and investigate if unsuccessful pulpotomy treatment in oncologic patients may lead to systemic complications. ProcedureTwenty-six medical records of children from a paediatric oncology referral centre who had dental pulpotomy treatment (in 41 teeth) while receiving active cancer care during the years 2006-2012 were compared with records of 41 randomly selected healthy children who had undergone pulpotomy treatment (41 teeth) in the same institute during these years. Clinical and radiographic data were collected during treatments and at the end of the follow-up period (six months post dental treatment). ResultsNo statisticaly significant difference was found between pulpotomy success rate amongst the two groups. Treatments success rates in the study and control groups were 82.9% (5.9) and 90.2% (+/- 4.7), respectively. No patient in the study group suffered from sepsis from a dental origin during follow-up period. ConclusionsPulpotomy in paediatric cancer patients did not increase the risk for bacteremia or systemic complications from oral origin. We therefore recommend the re-evaluation of the current protocol for treating paediatric oncology patients. Pediatr Blood Cancer 2014;61:2297-2301. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:2297 / 2301
页数:5
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