Department of Internal Medical Nursing, Nursing Faculty, Hacettepe University, Ankara, Turkey.
Department of Internal Medical Nursing, Nursing Faculty, Hacettepe University, Ankara, Turkey.
Clin Breast Cancer. 2024 Feb;24(2):112-121. doi: 10.1016/j.clbc.2023.10.012. Epub 2023 Nov 3.
To determine the effects of oral cryotherapy (OC) on the anticipatory, and acute nausea and vomiting of patients with breast cancer who are receiving adjuvant chemotherapy.
Seventy eligible patients with breast cancer were assigned to 2 groups by stratified randomization. This parallel grouped, randomized, clinical trial used the ice application protocol. OC application for an intervention group (IG, n = 35) was performed in 3 stages: i) instructions on by the investigator at the hospital; ii) the implementation accompanied by the investigator at the hospital; iii) the individual application of at home by patients. The IG had been doing the application for 12 weeks. The patients in the control group (CG, n = 35) received standard care. Additionally, Rhodes Index of Nausea Vomiting, and Retching, and EORTC QLQ-C30 Life Quality Index were conducted on the first (T1 = cycle 1 day 0), second (T2 = cycle 2 day 21), third (T3 = cycle 3 day 42), and fourth (T4 = cycle 4 day 63) cycles of adjuvant chemotherapy.
The anticipatory nausea scores in the T2 and T4, IG were significantly lower than the CG (P < .05). In the T3, all symptom sub-dimensions except symptom occurrence (t = -0,48; P = .63) of the IG were significantly lower than those of the CG (P < .05). In the T1, T2, T3, and T4, acute nausea, acute vomiting, acute retching, and anticipatory retching scores, were significantly lower than the CG (P < .05).
OC alone was effective and safe for the treatment of nausea and vomiting. The results of this study showed the clinical applicability of OC in the management of nausea and vomiting.
确定口腔冷冻疗法(OC)对接受辅助化疗的乳腺癌患者预期性和急性恶心呕吐的影响。
通过分层随机化将 70 名符合条件的乳腺癌患者分配到 2 组。这是一项平行分组、随机临床试验,采用冰敷方案。OC 应用于干预组(IG,n = 35)分为 3 个阶段:i)由研究人员在医院进行指导;ii)在医院由研究人员陪同实施;iii)由患者在家中自行应用。IG 持续进行了 12 周的应用。对照组(CG,n = 35)接受标准护理。此外,在辅助化疗的第 1 个周期(T1 = 第 0 天)、第 2 个周期(T2 = 第 21 天)、第 3 个周期(T3 = 第 42 天)和第 4 个周期(T4 = 第 63 天),进行 Rhodes 恶心呕吐指数和 EORTC QLQ-C30 生活质量指数评估。
T2 和 T4 时,IG 的预期性恶心评分明显低于 CG(P <.05)。在 T3 时,IG 的除症状发生外的所有症状亚维度评分(t = -0.48;P =.63)均明显低于 CG(P <.05)。在 T1、T2、T3 和 T4 时,急性恶心、急性呕吐、急性干呕和预期性干呕评分均明显低于 CG(P <.05)。
OC 单独用于治疗恶心和呕吐是有效且安全的。本研究结果表明 OC 在恶心和呕吐管理中的临床适用性。