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Safety and Efficacy of Combined Injection of Pure-µ-Opioid Agonist with Tramadol as an Opioid Induction Agent for Opioid-Naïve Cancer Patients.
Sato, Tetsumi; Ono, Shigeki; Sato, Tetsu; Tanaka, Rei; Kamo, Yoshiko; Suzuki, Tomomi.
Afiliación
  • Sato T; Division of Palliative Medicine, Shizuoka Cancer Center, Shizuoka, Japan.
  • Ono S; Palliative Care Team, Shizuoka Cancer Center, Shizuoka, Japan.
  • Sato T; Division of Palliative Medicine, Shizuoka Cancer Center, Shizuoka, Japan.
  • Tanaka R; Palliative Care Team, Shizuoka Cancer Center, Shizuoka, Japan.
  • Kamo Y; Palliative Care Team, Shizuoka Cancer Center, Shizuoka, Japan.
  • Suzuki T; Department of Pharmacy, Shizuoka Cancer Center, Shizuoka, Japan.
Palliat Med Rep ; 5(1): 340-349, 2024.
Article en En | MEDLINE | ID: mdl-39144134
ABSTRACT

Background:

Tramadol is known to provide synergistic analgesia when used in combination with morphine.

Objectives:

The aims of this study were (1) to introduce an opioid combination therapy using pure-µ-opioid receptor agonist (OPI) + tramadol injections (OPI + tramadol) and (2) to elucidate safety and efficacy of this combination therapy for opioid-naïve cancer pain patients.

Methods:

Opioid-naïve patients referred to our palliative care team (in Japan) who were unable to take oral medications and received OPI + tramadol as opioid induction agents were retrospectively investigated on the electric medical chart. OPI + tramadol dosage was adjusted to achieve the patient's pain as Numerical Rating Scale ≤4/10 or Support Team Assessment Schedule-Japanese ≤1. Patients' demography, doses of OPI and tramadol administered, and adverse events were analyzed.

Results:

A total of 44 patients were included. The primary organs of malignancy were pancreas (11), stomach (5), lung (4), breast (4), liver (4), and others (13). OPI injections administered were hydromorphone (39), morphine (6), oxycodone (1), and fentanyl (1). The starting doses of OPI (morphine equivalent) and tramadol were 6.05 ± 1.63 and 67.8 ± 13.6 mg/day, respectively, and the final doses of OPI (morphine equivalent) and tramadol were 8.14 ± 3.85 and 80.0 ± 28.5 mg/day, respectively. Treatment goals were achieved in all patients. There were three patients in whom OPI was switched owing to inadequate analgesia and no new side effects other than those known to occur when OPI or tramadol is administered appeared.

Conclusion:

The results suggest that this innovative and unique opioid therapy can be safely and effectively introduced to opioid-naïve cancer patients who are relatively close to the end of life.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Palliat Med Rep Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Palliat Med Rep Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos