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[Conversion to tapentadol PR improves analgesia and quality of life in patients with severe and chronic pain despite using tramadol > 300 mg/d]. / Konsekutive Umstellung auf Tapentadol PR verbessert Analgesie und Lebensqualität bei Patienten mit starken und chronischen Schmerzen unter Tramadol > 300 mg/d.
Richter, Uwe; Waldmann-Rex, Susanne; Lehmann, Ute.
Afiliação
  • Richter U; Palliativmedizin. Med. Versorgungszentrum Spez. Schmerztherapie und Palliativmedizin am DRK Krankenhaus, Chemnitz-Rabenstein, Deutschland.
Wien Klin Wochenschr ; 127(11-12): 477-87, 2015 Jun.
Article em De | MEDLINE | ID: mdl-25409951
ABSTRACT
STUDY

OBJECTIVE:

This subgroup analysis of a non-interventional study involving general practitioners and internists investigated the administration of tapentadol PR (prolonged release) in patients with widely-utilized tramadol pretreatment in routine clinical practice in Germany.

METHODS:

Data of all patients in the study cohort who had tramadol as the only opioid in their previous therapy were included in the analysis (n = 685); among them especially the 99 patients with tramadol dosages exceeding 300 mg/d were focused. Data collection during the 3-month observation period included previous and concomitant analgesic treatment, tapentadol PR dosage, pain intensity, sleep and quality of life parameters, and tolerability of tapentadol PR.

RESULTS:

Back pain was the most common cause of pain (n = 86/99), other pain diagnoses were (partly additionally) recorded in 68 cases. A mixed type of pain dominated. The previous tramadol therapy was usually combined with non-opioids (n = 74), co-analgesics (n = 44) and analgesic rescue medication (n = 35). Tapentadol PR therapy reduced the mean initial pain intensity of 7.3 ± 1.5 to 3.1 ± 1.8 points (NRS-11, 11-point pain scale, n = 96) at the end of observation, using an average dosage of 218.7 mg/d. Tapentadol PR was finally applied as the sole analgesic in 32/95 patients. 69/96 patients achieved a clinically meaningful pain relief of at least 50 %, while 63 patients gained a pain reduction of ≥ 4 NRS-points. 89/95 patients reached or exceeded their additional individual treatment goal. This was accompanied by a significant decrease in pain-related impairments of daily activities and an improvement in quality of life with an overall good tolerability of tapentadol PR. Treatment with tapentadol PR was assessed positively by physicians and patients.

CONCLUSIONS:

Data analysis shows a clinically relevant benefit in patients unsuccessfully pretreated with tramadol by consecutive conversion to the potent analgesic tapentadol PR.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenóis / Qualidade de Vida / Tramadol / Medição da Dor / Dor Crônica Tipo de estudo: Clinical_trials Limite: Aged / Female / Humans / Male / Middle aged Idioma: De Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenóis / Qualidade de Vida / Tramadol / Medição da Dor / Dor Crônica Tipo de estudo: Clinical_trials Limite: Aged / Female / Humans / Male / Middle aged Idioma: De Ano de publicação: 2015 Tipo de documento: Article