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Chiou T–J et al. – From 2005 to 2006, 822 outpatients received TTS–F to collect pain assessment forms and diaries for 4 weeks. Most (78.7%) patients were initially prescribed 25 microg/h TTS–F. Doses were adjusted weekly at clinicians' discretion, according to pain assessment and side effects. Patients receiving 50 microgg/h, 75 microgg/h, and > 75 microgg/h TTS–F had increased from 17.5% to 32.1%, 1.8% to 3.4%, and 1.9% to 2.2%, respectively, by week 2; further small increases were found in weeks 3 and 4. Pain palliation improved from 60.6% during week 1 to 78.6% at week 4. The common adverse effects were nausea/vomiting. Patient’s compliance was >90%. This study found that the TTS–F is effective and well tolerated.

Exclusive Author Commentary
Tzeon-Jye Chiou, 10/05/09

This is the first article to describe the use of TTS-F in the treatment of pain in advanced cancer patients in Taiwan. It is a valuable article to describe the use of TTS-F as a fist step or second step to treat cancer pain in advanced cancer patients. The result just shows us that the early use of TTS-F in cancer pain is worthful for cancer pain and results in lower incidence of opioid related toxicity.

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