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Fentanyl Buccal Tablet: A New Breakthrough Pain Medication in Early Management of Severe Vaso‐Occlusive Crisis in Sickle Cell Disease
Author(s) -
De Franceschi Lucia,
Mura Paolo,
Schweiger Vittorio,
Vencato Elisa,
Quaglia Francesca Maria,
Delmonte Letizia,
Evangelista Maurizio,
Polati Enrico,
Olivieri Oliviero,
Finco Gabriele
Publication year - 2016
Publication title -
pain practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 58
eISSN - 1533-2500
pISSN - 1530-7085
DOI - 10.1111/papr.12313
Subject(s) - medicine , vaso occlusive crisis , anesthesia , tramadol , fentanyl , sickle cell anemia , crossover study , opioid , acute pain , disease , analgesic , pathology , alternative medicine , receptor , placebo
Background Sickle cell disease ( SCD ) is a worldwide distributed hereditary red cell disorder. The principal clinical manifestations of SCD are the chronic hemolytic anemia and the acute vaso‐occlusive crisis ( VOC s), which are mainly characterized by ischemic/reperfusion tissue injury. Pain is the main symptom of VOC s, and its management is still a challenge for hematologists, requiring a multidisciplinary approach. Methods We carried out a crossover study on adult SCD patients, who received two different types of multimodal analgesia during two separate severe VOC s with time interval between VOC s of at least 6 months. The first VOC episode was treated with ketorolac (0.86 mg/kg/day) and tramadol (7.2 mg/kg/day) ( TK treatment). In the second VOC episode, fentanyl buccal tablet ( FBT ; 100 μg) was introduced in a single dose after three hours from the beginning of TK analgesia ( TKF treatment). We focused on the first 24 hours of acute pain management. The primary efficacy measure was the time‐weighted‐sum of pain intensity differences ( SPID 24). The secondary efficacy measures included the pain intensity difference ( PID ), the total pain relief ( TOTPAR ), and the time‐wighted sum of anxiety ( SAID 24). Results SPID 24 was significantly higher in TKF than in TK treatment. All the secondary measures were significantly ameliorated in TKF compared to TK treatment, without major opioid side effects. Patients satisfaction was higher with TKF treatment than with TK one. Conclusions We propose that VOC s might require breakthrough pain drug strategy as vaso‐occlusive phenomena and enhanced vasoconstriction promoting acute ischemic pain component exacerbate the continuous pain of VOC s. FBT might be a powerful and feasible tool in early management of acute pain during VOC s in emergency departments.