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A Comparison of the Clinical Effectiveness Between Low-Dose Strong Opioids and Non-Steroidal Anti-Inflammatory Drugs in the Treatment of Mild Cancer Pain: A Randomized Trial.
Liu, Mei-Zuo; Ma, Jian; Li, Jun-Dong; Sun, Jing; Zhou, Hua; Guan, Shuo; Han, Ying; Zhang, Xia; Bian, Ji-Lai.
Afiliação
  • Liu MZ; Department of Oncology, The Fifth People's Hospital of Dalian, Dalian, 116000, People's Republic of China.
  • Ma J; Intensive Care Unit, The Fifth People's Hospital of Dalian, Dalian, 116000, People's Republic of China.
  • Li JD; Department of Oncology, The Fifth People's Hospital of Dalian, Dalian, 116000, People's Republic of China.
  • Sun J; Department of Oncology, The Fifth People's Hospital of Dalian, Dalian, 116000, People's Republic of China.
  • Zhou H; Department of Oncology, The Fifth People's Hospital of Dalian, Dalian, 116000, People's Republic of China.
  • Guan S; Department of Oncology, The Fifth People's Hospital of Dalian, Dalian, 116000, People's Republic of China.
  • Han Y; Department of Oncology, The Fifth People's Hospital of Dalian, Dalian, 116000, People's Republic of China.
  • Zhang X; Medical Examination Center, The Fifth People's Hospital of Dalian, Dalian, 116000, People's Republic of China.
  • Bian JL; Department of Oncology, The Fifth People's Hospital of Dalian, Dalian, 116000, People's Republic of China.
J Pain Res ; 14: 3411-3419, 2021.
Article em En | MEDLINE | ID: mdl-34754234
ABSTRACT

OBJECTIVE:

The present study aims to explore the effectiveness and safety of low-dose strong opioids compared with non-steroidal anti-inflammatory drugs (NSAIDs) in the treatment of mild cancer pain.

METHODS:

From September 2016 to September 2018, 66 patients with a malignant tumor and mild cancer pain admitted to the Department of Oncology of Dalian Fifth People's Hospital were divided into the group A (treated with ibuprofen sustained-release tablets for pain relief) and the group B (treated with oxycodone hydrochloride sustained-release tablets for pain relief). After 7 days of treatment, the pain relief (Numeric Rating Scale [NRS]), physical strength, quality of life scores (Zubrod/ECOG/WHO [ZPS]), the Edmonton Symptom Assessment System [ESAS], and the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core15-Palliative [EORTC QLQ-C15-PAL] scores), and the occurrence of adverse reactions between the two groups were compared. The occurrence of adverse reactions in the mid-term (after one month and three months of treatment) between the two groups were also compared.

RESULTS:

Both groups had over 90% analgesic efficiency, but complete pain relief was more likely to be obtained in the group B (41.18%). The total analgesic efficiency in the group B was higher (100%) than in the group A (98.9%), and the difference was statistically significant (P < 0.05). The differences in the physical strength and quality of life scores in the two groups before and after treatment were statistically significant (P < 0.05). The differences in the ZPS scores between the two groups were statistically significant (P < 0.05). The differences in ESAS and EORTC QLQ-C15-PAL scores between groups were not statistically significant (P > 0.05).

CONCLUSION:

The application of low-dose oxycodone hydrochloride sustained-release tablets as the initial medication for patients with mild cancer pain was safe and effective, and the adverse reactions were easy to manage.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Aspecto: Patient_preference Idioma: En Revista: J Pain Res Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Aspecto: Patient_preference Idioma: En Revista: J Pain Res Ano de publicação: 2021 Tipo de documento: Article