지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2019.12
- 수록면
- 147 - 153 (7page)
이용수
초록· 키워드
오류제보하기
Purpose: The aims of this study were to investigate the expectation of patients with burning mouth syndrome (BMS) and assess the relationship between patient expectations and clinical and psychological characteristics.
Methods: Eligibility was retrospectively assessed on 93 patients with BMS. A total of five questionnaires on patients’ expectation for a visit, pain, sleep quality (Pittsburgh Sleep Quality Index), cognition (Pain Catastrophizing Scale) and psychological distress (Symptom Checklist-90 revised) were measured.
Results: Sixty-five patients were included in this study. The top 3 priorities of expectation for a treatment visit to the Department of Oral Medicine were as following; “I want my pain to be free”; “I want to understand why it hurts”; “I want to communicate better with doctors about pain”. Patients with priority of pain relief showed poor sleep quality than patients who are more interested in the disease related information.
Conclusions: To improve treatment outcomes of BMS, clinicians should improve their own understanding of patients who are suffering from BMS. Inquiring about the patient expec-tations may be one of them, and it would contribute to the enhancement of patients’ overall well-being.
Methods: Eligibility was retrospectively assessed on 93 patients with BMS. A total of five questionnaires on patients’ expectation for a visit, pain, sleep quality (Pittsburgh Sleep Quality Index), cognition (Pain Catastrophizing Scale) and psychological distress (Symptom Checklist-90 revised) were measured.
Results: Sixty-five patients were included in this study. The top 3 priorities of expectation for a treatment visit to the Department of Oral Medicine were as following; “I want my pain to be free”; “I want to understand why it hurts”; “I want to communicate better with doctors about pain”. Patients with priority of pain relief showed poor sleep quality than patients who are more interested in the disease related information.
Conclusions: To improve treatment outcomes of BMS, clinicians should improve their own understanding of patients who are suffering from BMS. Inquiring about the patient expec-tations may be one of them, and it would contribute to the enhancement of patients’ overall well-being.
목차
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES
참고문헌 (19)
참고문헌 신청
IASP orofacial pain fact sheet
Feller L / 2017 / Burning mouth syndrome: aetiopathogenesis and principles of management / Pain Res Manag 2017:1926269
Souza FT / 2011 / The impact of burning mouth syndrome on health-related quality of life / Health Qual Life Outcomes 9:57
López-Jornet P / 2008 / Quality of life in patients with burning mouth syndrome / J Oral Pathol Med 37:389~394
Ni Riordain R / 2010 / Burning mouth syndrome and oral health-related quality of life: is there a change over time? / Oral Dis 16:643~647
Feller L / 2017 / Burning mouth syndrome: aetiopathogenesis and principles of management / Pain Res Manag 2017:1926269
Souza FT / 2011 / The impact of burning mouth syndrome on health-related quality of life / Health Qual Life Outcomes 9:57
López-Jornet P / 2008 / Quality of life in patients with burning mouth syndrome / J Oral Pathol Med 37:389~394
Ni Riordain R / 2010 / Burning mouth syndrome and oral health-related quality of life: is there a change over time? / Oral Dis 16:643~647
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