Pawlaczyk-Kamieńska Tamara, Borysewicz-Lewicka Maria, Batura-Gabryel Halina, Cofta Szczepan
Department of Risk Group Dentistry, Chair of Pediatric Dentistry, Poznan University of Medical Sciences, 61-701 Poznan, Poland.
Department of Pulmonology, Allergology and Respiratory Oncology, Poznan University of Medical Sciences, 60-569 Poznan, Poland.
J Clin Med. 2022 May 13;11(10):2756. doi: 10.3390/jcm11102756.
Cystic fibrosis (CF) is a genetic disease that is caused by a defect in the gene coding for the transmembrane cystic fibrosis transmembrane conductance regulator (CFTR). Research papers published so far point out that despite the numerous dental treatment needs of CF patients, there are no oral care guidelines for this group of patients. The aim of the article is to propose standards of dental prophylactic and therapeutic procedures for CF patients in different age groups. Regardless of the CF patient's age, dental check-ups should be scheduled at least every 6 months. However, taking into account the actual condition of the individual CF patients, therapeutic visits may be scheduled for earlier dates, to provide well-fitting treatment, considering the level of risk of oral diseases. The described management standards may be helpful and may improve the quality of dental care provided to CF patients.
囊性纤维化（CF）是一种遗传性疾病，由编码跨膜囊性纤维化跨膜传导调节因子（CFTR）的基因缺陷引起。迄今为止发表的研究论文指出，尽管CF患者有众多的牙科治疗需求，但针对这组患者尚无口腔护理指南。本文的目的是为不同年龄组的CF患者提出牙科预防和治疗程序的标准。无论CF患者的年龄如何，牙科检查应至少每6个月安排一次。然而，考虑到个别CF患者的实际情况，治疗就诊可能需要安排得更早，以便根据口腔疾病的风险程度提供合适的治疗。所述的管理标准可能会有所帮助，并可能提高为CF患者提供的牙科护理质量。
