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囊性纤维化患者的口腔护理建议——给牙医的建议

Oral Care Recommendation for Cystic Fibrosis Patients-Recommendation for Dentists.

作者信息

Pawlaczyk-Kamieńska Tamara, Borysewicz-Lewicka Maria, Batura-Gabryel Halina, Cofta Szczepan

机构信息

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.

出版信息

J Clin Med. 2022 May 13;11(10):2756. doi: 10.3390/jcm11102756.

Abstract

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.

摘要

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。

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Periodontal health.牙周健康。
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J Oral Rehabil. 2018 Sep;45(9):730-746. doi: 10.1111/joor.12664. Epub 2018 Jun 25.
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Epigenetic regulation of CFTR in salivary gland.唾液腺中囊性纤维化跨膜传导调节因子的表观遗传调控
Biochem Biophys Res Commun. 2016 Dec 2;481(1-2):31-37. doi: 10.1016/j.bbrc.2016.11.023. Epub 2016 Nov 8.

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