Consequences of Poor Access to Dental Care in Adult Patients with Sickle Cell Disease
Journal Title: Journal of Blood Disorders & Transfusion - Year 2018, Vol 9, Issue 3
Abstract
Sickle cell disease (SCD) is the most prevalent genetic disease in the United States. The patients with SCD areprone to dental problems due to vasoocclusion, increased risk of infection and structural bone changes. There areno specific guidelines for the management of dental problems in SCD. We did a survey on adult patients with SCDto evaluate the prevalence of patient reported dental problems, including existing “bad tooth”, and tooth abscess. Wealso investigated the prevalence of dental insurance that pays for regular dental exams. We found that, only 33%had their last dental exam within a year and a third of them had more than 2 adult teeth removed. Large number(41%) of the patients reported that they currently had tooth ache or have a bad tooth. We also found that only 33%of the adults with SCD had the dental insurance to pay for dental care. On further analysis, it was found that adultswith dental insurance had more dental exams and fewer episodes of dental abscess or bad teeth. Dental careremains a significant unmet need in this special population who are at risk of various dental disorde
Authors and Affiliations
Samip Master, Richard Preston Mansour
Consequences of Poor Access to Dental Care in Adult Patients with Sickle Cell Disease
Sickle cell disease (SCD) is the most prevalent genetic disease in the United States. The patients with SCD areprone to dental problems due to vasoocclusion, increased risk of infection and structural bone changes. There...
Assessment of Knowledge, Attitude and Practice of Graduating Health Science Students towards Blood Donation at Wolaita Soddo University
Background: Adequate quantity of blood is considered necessary to receive adequate oxygen and nutrients and to carry out certain function. A huge volume of blood can be lost as a result of various medical, obstetrics or...
Heterozygous Haemoglobin C/Beta Thalassemia: About a Fortuitous Discovery Case
Haemoglobin C is a genetic disorder caused by the synthesis of abnormal haemoglobin (Hbc) that replaceshaemoglobin A. We report in our observation a case of a 50-years-old woman with heterozygous haemoglobin C/beta thala...
Anesthetic Considerations of a Surgical Patient with Favism: A Case Report
Rationale: Favism is a genetic disease of Glucose 6 phosphatase dehydrogenase (G6PD) deficiency in humanred blood cells. It is mainly due to the mutation of G6PD gene encoded on the X chromosome, which leads to thedecrea...
A Rare Case of Saudi Girl with Recurrent Strokes and Abnormal Multiple Thrombophilia
Recurrent multiple symptomatic strokes are infrequent in paediatric population. The causes for such events areusually cardiac, multiple inherited thrombophilia; such as Protein C, Protein S, Antithrombin III, and Antipho...