Evaluation of pain associated with oral mucositis during the acute period after administration of high-dose chemotherapy

被引:41
作者
Cella, D
Pulliam, J
Fuchs, H
Miller, C
Hurd, D
Wingard, JR
Sonis, ST
Martin, PJ
Giles, F
机构
[1] Evanston NW Healthcare Res Inst, Inst Hlth Serv Res & Policy Studies, CORE, Evanston, IL 60201 USA
[2] Northwestern Univ, Evanston, IL USA
[3] IntraBiotics Pharmaceut Inc, Mountain View, CA USA
[4] Johns Hopkins Oncol Ctr, Baltimore, MD USA
[5] Wake Forest Univ, Ctr Comprehens Canc, Winston Salem, NC 27109 USA
[6] Univ Florida, Coll Med, Dept Med, Gainesville, FL USA
[7] Brigham & Womens Hosp, Div oral Med Oral & Maxillofacial Surg & Dent, Dept Surg, Boston, MA 02115 USA
[8] Univ Washington, Dept Med, Seattle, WA 98195 USA
[9] MD Anderson Canc Ctr, Dept Leukemia, Houston, TX USA
关键词
oral mucositis; stomatitis; dysphagia; oral pain; iseganan HCl;
D O I
10.1002/cncr.11505
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. No single oral mucositis (OM) assessment scale is universally accepted; the most commonly used scales are deficient because they combine subjective and objective measures and do not capture the patient's perspective. Because pain is the hallmark symptom of OM, the authors sought to determine whether a simple measure of patient-reported pain was correlated with objective, physician-assessed measures of OM. The findings of the current study may provide a clinical context for understanding the relation between objective indicators and patients' perceptions of OM. METHODS. Three hundred twenty-three patients receiving stomatotoxic chemotherapy and randomized to receive either iseganan or placebo for treatment of OM underwent periodic objective and subjective evaluations of OM. Objective measures included clinician scoring of stomatitis and dysphagia using the National Cancer Institute Common Toxicity Criteria scales. A subjective measure was obtained by having patients complete a questionnaire (with questions based on an 11-point numeric scale) regarding oral pain. RESULTS. More than 90% of scheduled oral assessments were obtained. Mouth pain scores were closely related to stomatitis and dysphagia; peak mouth pain coincided with peak stomatitis and dysphagia. Analgesic use increased by 0.7 days for each unit rise on the pain scale. Patients receiving iseganan had a significantly lower level of peak mouth pain than did patients receiving placebo (P = 0.041). CONCLUSIONS. A separate measurement of patient-reported pain was useful for capturing the patient's perspective on OM and was correlated with the physician's objective assessment. These findings support the use of a simple, patient-reported rating of mouth pain as a clinically relevant and responsive endpoint in clinical trials. This rating system also may provide a straightforward method of following OM in clinical practice. (C) 2003 American Cancer Society.
引用
收藏
页码:406 / 412
页数:7
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