𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Long-acting morphine for pain control in paediatric oncology

✍ Scribed by Zernikow, Boris ;Lindena, Gabriele


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
180 KB
Volume
36
Category
Article
ISSN
0098-1532

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Background

Guidelines for treatment of paediatric cancer pain recommend the usage of long‐acting morphine. However, published paediatric experience with this drug is restricted to 147 children not systematically evaluated, and thus insufficient. We aimed to systematically analyse the age‐dependent effects and adverse effects of long‐acting morphine in paediatric cancer patients.

Procedure

Ninety‐five children aged 1 to 19 years were enrolled in a collaborative retrospective study conducted over seven‐and‐a‐half years. Pain was scored according to a numeric rating scale (NRS, range 0 to 5), and the corresponding medication was recorded.

Results

In 83 children documentation period started during morphine treatment (71, oral long‐acting; 1, rectal; 11, IV). Mean oral/equivalent morphine starting dose was 1.3 mg/kgbw/d (SD 0.9). Mean end dose was 2.8 mg/kgbw/d (SD 2.7). Infants aged < 7 years received the highest average dose (2.6 mg/kgbw/d, SD 2.8), while patients > 12 years received the lowest dose (1.4 mg/kgbw/d, SD 1.1). Median pain intensity decreased from score 1.0 (mean 1.2) NRS at the beginning to 0 (mean 0.6) NRS at the end. The proportion of patients scoring > 2 NRS (severe or most severe pain) under morphine treatment decreased from 26 to 12% (P = 0.08). In children > 12 years pruritus was frequently observed (23% of patients). In all age groups, there were no severe adverse effects during the study period.

Conclusions

In paediatric haematology/oncology, pain control by oral long‐acting morphine proved to be safe and effective even in the very young patients. The pharmacological properties of long‐acting morphine are ideally suited for paediatric use, combining efficacy and compatibility. Med. Pediatr. Oncol. 36:451–458, 2001. © 2001 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Dextromethorphan for the reduction of im
✍ Avi A. Weinbroum; Alexander Gorodetzky; Alexander Nirkin; Yehuda Kollender; Jaco 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 97 KB 👁 1 views

## Background: Postoperative pain is mediated centrally by n-methyl-d-aspartate (nmda) receptors. the beneficial effects of preincision oral dextromethorphan (dm), which is an nmda antagonist, on postoperative pain and intravenous patient-controlled analgesia (iv-pca) morphine (mo) consumption have

Intrathecal morphine combined with intra
✍ Justin Sangwook Ko; Soo Joo Choi; Mi Sook Gwak; Gaab Soo Kim; Hyun Joo Ahn; Jie 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 248 KB

The healthy condition of living donors makes their tolerance to pain particularly low, and clinicians are often challenged to come up with an analgesic technique that is effective yet ensures donor safety. This study compared, in donor right hepatectomy, the efficacy and safety of preoperative intra