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2.
Pain Med ; 16(12): 2338-43, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26301791

RESUMO

OBJECTIVE: To evaluate the durability of pain relief provided by a new formulation of single-entity, hydrocodone extended-release (ER) (Zohydro(®) ER) throughout the 12-hour dosing interval by examining patterns of rescue medication use. DESIGN: Phase 3, enriched enrollment, randomized withdrawal study with an open-label, conversion/titration phase (≤6 weeks) followed by a placebo-controlled, double-blind treatment phase (12 weeks). SETTING: Fifty-seven study sites in the United States enrolled patients. SUBJECTS: One hundred and fifty-one opioid-experienced subjects with moderate to severe chronic low back pain who were treated with hydrocodone ER once every 12 hours. METHODS: Post hoc analysis of rescue medication use by frequency and distribution of use following the morning and evening dose of hydrocodone ER. RESULTS: No rescue medication was used following the morning or evening dose of hydrocodone ER during 36.0% and 76.7% of the dosing days, respectively. Time distribution of rescue medication use showed that 79.3% of all rescue medication doses were administered following the morning dose, with the highest rate of usage (46.2%) occurring 4-8 hours postdose, followed by 18.7% and 14.4% usage 0-4 and 8-12 hours postdose, respectively. Examination of the three 4-hour intervals following the evening dose of hydrocodone ER revealed similar minimal rescue medication use (5.6-8.2%). CONCLUSIONS: End-of-dose failure was not observed based on the use of rescue medication after administration of single-entity, twice daily, hydrocodone ER capsules (Zohydro ER).


Assuntos
Dor Crônica/diagnóstico , Dor Crônica/tratamento farmacológico , Hidrocodona/administração & dosagem , Dor Lombar/diagnóstico , Dor Lombar/tratamento farmacológico , Medição da Dor/efeitos dos fármacos , Adolescente , Adulto , Idoso , Analgésicos Opioides/administração & dosagem , Método Duplo-Cego , Esquema de Medicação , Feminino , Humanos , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Efeito Placebo , Resultado do Tratamento , Estados Unidos , Adulto Jovem
3.
J Natl Compr Canc Netw ; 11(8): 992-1022, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23946177

RESUMO

Pain is a common symptom associated with cancer and its treatment. Pain management is an important aspect of oncologic care, and unrelieved pain significantly comprises overall quality of life. These NCCN Guidelines list the principles of management and acknowledge the range of complex decisions faced in the management oncologic pain. In addition to pain assessment techniques, these guidelines provide principles of use, dosing, management of adverse effects, and safe handling procedures of pharmacologic therapies and discuss a multidisciplinary approach for the management of cancer pain.


Assuntos
Neoplasias/terapia , Manejo da Dor/métodos , Dor/complicações , Acetaminofen/uso terapêutico , Analgésicos Opioides/uso terapêutico , Anti-Inflamatórios não Esteroides/uso terapêutico , Humanos , Dor/tratamento farmacológico , Medição da Dor , Apoio Social
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