期刊论文详细信息
BMC Clinical Pharmacology
Cohort study of consistency between the compliance with guidelines for chemotherapy-induced nausea and vomiting and patient outcome
Hiroyuki Shibata2  Masatomo Miura1  Kazunori Otsuka2  Naomi Shindo2  Manabu Shoji1  Masahiro Inoue2 
[1] Department of Pharmacy, Akita University, Akita, Japan;Division of Chemotherapy for Outpatient, Akita University, Akita, Japan
关键词: Emetogenicity;    Guidelines;    Chemotherapy-induced nausea and vomiting;   
Others  :  1145164
DOI  :  10.1186/s40360-015-0005-1
 received in 2014-10-09, accepted in 2015-03-12,  发布年份 2015
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【 摘 要 】

Background

Chemotherapy-induced nausea and vomiting is one of the most influential factors that affect patient quality of life; thus, preventing this adverse event could lead to better patient outcome. Standard preventive guidelines for antiemetic treatment have already been established based on the emetogenicity of chemotherapeutic agents. It is important that compliance with in-house guidelines and their effect on patient outcome is monitored.

Methods

In 3 years since the Akita university hospital antiemetic guidelines were outlined, we assessed the incidence of chemotherapy-induced nausea and vomiting using the antiemesis tool of the Multinational Association of Supportive Care in Cancer. Compliance of the guidelines was extracted from the hospital clinical record, and the chemotherapy-induced nausea and vomiting was examined by the patient reported outcome.

Results

Seventy-three patients answered the questionnaire. The overall compliance rate with the guidelines for early nausea and vomiting was 98.6% and with the delayed nausea and vomiting was 87.7%. The complete response rate for the early and delayed chemotherapy-induced nausea and vomiting was 77.8% and 73.8%, respectively. The overall relative risk of early nausea and vomiting was 0.22 (P < 0.05), whereas the relative risk for delayed nausea and vomiting was 2.09 (P < 0.05). Breakthrough vomiting was observed in 3 cases in the low-risk group only. These data suggest that delayed nausea and vomiting is difficult to prevent, particularly in the low-risk group. Further, it seems that the individual sensitivity for emetogenicity might differ among patients.

Conclusions

In addition to standard prevention guidelines based on emetogenicity, individual care based on patient reports should be considered for the complete prevention of chemotherapy-induced nausea and vomiting.

【 授权许可】

   
2015 Inoue et al.; licensee BioMed Central.

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【 参考文献 】
  • [1]Morran C, Smith DC, Anderson DA, McArdle CS: Incidence of nausea and vomiting with cytotoxic chemotherapy: a prospective randomised trial of antiemetics. Br Med J 1979, 1:1323-4.
  • [2]Richardson JL, Marks G, Levine A: The influence of symptoms of disease and side effects of treatment on compliance with cancer therapy. J Clin Oncol 1988, 6:1746-52.
  • [3]Baker PD, Morzorati SL, Ellett ML: The pathophysiology of chemotherapy-induced nausea and vomiting. Gastroenterol Nurs 2005, 28:469-80.
  • [4]Basch E, Prestrud AA, Hesketh PJ, Kris MG, Feyer PC, Somerfield MR, et al.: American Society of Clinical Oncology guideline for antiemetics in oncology: update 2006. J Clin Oncol 2006, 24:2932-47.
  • [5]Aapro M, Fabi A, Nolè F, Medici M, Steger G, Bachmann C, et al.: Double-blind, randomised, controlled study of the efficacy and tolerability of palonosetron plus dexamethasone for 1 day with or without dexamethasone on days 2 and 3 in the prevention of nausea and vomiting induced by moderately emetogenic chemotherapy. Ann Oncol 2010, 21:1083-8.
  • [6]Gralla RJ, De Wit R, Herrstedt J, Carides AD, Ianus J, Guoguang-Ma J, et al.: Antiemetic efficacy of the neurokinin-1 antagonist, aprepitant, plus a 5-HT3 antagonist and a corticosteroid in patients receiving anthracy-clines or cyclophosphamide in addition to high-dose cisplatin: analysis of combined data from two phase III randomized clinical trials. Cancer 2005, 104:864-8.
  • [7]Jordan K, Sippel C, Schmoll HJ: Guidelines for antiemetic treatment of chemotherapy-induced nausea and vomiting: past, present, and future recommendations. Oncologist 2007, 12:1143-50.
  • [8]Liau CT, Chu NM, Liu HE, Deuson R, Lien J, Chen JS: Incidence of chemotherapy-induced nausea and vomiting in Taiwan: physicians’ and nurses’ estimation vs. patients’ reported outcomes. Support Care Cancer 2005, 13:277-86.
  • [9]MASCC Antiemesis Tool© (MAT) [http://www.mascc.org/mat]
  • [10]Caracuel F, Muñoz N, Baños U, Ramirez G. Adherence to antiemetic guidelines and control of chemotherapy-induced nausea and vomiting (CINV) in a large hospital. J Oncol Pharm Pract. 2014. [Epub ahead of print].
  • [11]Keat CH, Phua G, Abdul Kassim MS, Poh WK, Sriraman M: Can granisetron injection used as primary prophylaxis improve the control of nausea and vomiting with low-emetogenic chemotherapy? Asian Pac J Cancer Prev 2013, 14:469-73.
  • [12]Jones JM, Qin R, Bardia A, Linquist B, Wolf S, Loprinzi CL: Antiemetics for chemotherapy-induced nausea and vomiting occurring despite prophylactic antiemetic therapy. J Palliat Med 2011, 14:810-4.
  • [13]Bouganim N, Dranitsaris G, Hopkins S, Vandermeer L, Godbout L, Dent S, et al.: Prospective validation of risk prediction indexes for acute and delayed chemotherapy-induced nausea and vomiting. Curr Oncol 2012, 19:e414-21.
  • [14]Kris MG, Roila F, De Mulder PH, Marty M: Delayed emesis following anticancer chemotherapy. Support Care Cancer 1998, 6:228-32.
  • [15]Kim HK, Hsieh R, Chan A, Yu S, Han B, Gao Y, et al. Impact of CINV in earlier cycles on CINV and chemotherapy regimen modification in subsequent cycles in Asia Pacific clinical practice. Support Care Cancer. 2014. [Epub ahead of print].
  • [16]Molassiotis A, Stamataki Z, Kontopantelis E: Development and preliminary validation of a risk prediction model for chemotherapy-related nausea and vomiting. Support Care Cancer 2013, 21:2759-67.
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