Frequency, severity, and impact on daily life of delayed and intercycle chemotherapy-induced nausea, vomiting, and retching.


Journal

Tumori
ISSN: 2038-2529
Titre abrégé: Tumori
Pays: United States
ID NLM: 0111356

Informations de publication

Date de publication:
Dec 2021
Historique:
pubmed: 5 2 2021
medline: 15 12 2021
entrez: 4 2 2021
Statut: ppublish

Résumé

Chemotherapy-induced nausea, vomiting, and retching (CINVR) remains a common side effect of treatment. Most previous studies have focused on vomiting control; nausea and retching have been less explored. This study aimed at describing the incidence, severity, and impact on daily life (IDL) of CINVR in the acute (0-24 hours), delayed (>24-120 hours), and overall (0-120 hours) postchemotherapy periods and beyond 120 hours (until next chemotherapy administration); and the pharmacologic and nonpharmacologic strategies adopted by patients to relieve symptoms. This was a single-center, cross-sectional study of 60 patients undergoing chemotherapy. Participants reported the frequency, severity, and IDL of CINVR from the day of chemotherapy administration up to 120 hours thereafter and nausea and vomiting that occurred beyond 120 hours, as well as pharmacologic and nonpharmacologic remedies used. Forty-seven (78.3%, 95% confidence interval [CI] 66.4-86.9), 37 (61.7%, 95% CI 49.0-72.9), and 35 (58.3%, 95% CI 45.7-69.9) patients reported no nausea (Numeric Rating Scale ⩽1), vomiting, or retching in the acute, delayed, and overall periods, respectively. Nausea was more frequent, more severe, and had a greater IDL than did vomiting and retching across the overall observation period; beyond 120 hours, 11 (18.3%, 95% CI 10.6-29.9) patients reported nausea and none reported vomiting, with a median IDL of 1/10 (interquartile range: 0.75-5.00; 95% CI 0-7.6). Metoclopramide (n = 57 administrations), dexamethasone (n = 28), eating small servings of food (n = 13), and aloe (n = 11) were the most commonly used rescue therapies. Future studies should set hard outcomes, such as the absence of any symptoms, as a primary end point, and these should be assessed across and beyond the 120-hour period.

Identifiants

pubmed: 33535920
doi: 10.1177/0300891621990434
doi:

Substances chimiques

Antiemetics 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

571-577

Auteurs

Silvia Gonella (S)

Department of Public Health and Pediatrics, University of Torino, Torino, Italy.
Direction of Health Professions, Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino, Torino, Italy.

Dino S Di Massimo (DS)

Direction of Health Professions, Biella Hospital, Ponderano (BI), Italy.

Marinella Mistrangelo (M)

Piedmont and Aosta Valley Oncological Inter-Regional Network, Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino, Torino, Italy.

Gianmauro Numico (G)

Oncological ward, Medical Department, Azienda Ospedaliera Santa Croce e Carle, Cuneo (CN), Italy.

Paola Berchialla (P)

Department of Clinical and Biological Sciences, University of Torino, Torino, Italy.

Paola Di Giulio (P)

Department of Public Health and Pediatrics, University of Torino, Torino, Italy.

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