Safety and efficacy of ketorolac continuous infusion for multimodal analgesia of vaso-occlusive crisis in patients with sickle cell disease

被引:0
|
作者
Valeria Maria Pinto
Barbara Gianesin
Salvatore Sardo
Filippo Mazzi
Giammarco Baiardi
Sofia Menotti
Fabio Piras
Sabrina Quintino
Giacomo Robello
Francesca Mattioli
Gabriele Finco
Gian Luca Forni
Lucia De Franceschi
机构
[1] EO Ospedali Galliera,Department of Medical Science and Public Health
[2] For Anemia Foundation,Department of Medicine
[3] University of Cagliari,Department of Internal Medicine, Pharmacology & Toxicology Unit
[4] University of Verona and AOUI Verona,Clinical Pharmacology Unit
[5] University of Genoa,undefined
[6] EO Ospedali Galliera,undefined
关键词
Sickle cell disease; Ketorolac; Multi-modal analgesia; Pain;
D O I
暂无
中图分类号
学科分类号
摘要
Pain is an hallmark of sickle-cell-related acute clinical manifestations as part of acute vaso-occlusive crisis (VOC). In SCD pain has different origins such as vascular or neuropathic pain, which requires multimodal analgesia. This is based on the administration of drugs with different pharmacological mechanisms of action, maximizing analgesia and minimizing their adverse events and the risk of drug-addition in patients experiencing acute-recurrent pain events as in SCD. Ketorolac is a potent non-narcotic analgesic, being relatively safe and effective during pain-management in children and adults. Up to now, there is a lack of safety information on continuous infusion ketorolac as used to control acute pain in patients with SCD, and the benefits/risks ratio needs to be investigated. Here, we report for the first time the safety profile of ketorolac in the special population of patients with SCD. We confirmed that ketorolac in combination with tramadol, an opioid like molecule, is effective in pain control of adult patients with SCD experiencing acute severe VOCs defined by pain visual analog scale. Our study shows that short term (72 h) continuous infusion of ketorolac plus tramadol is not associated with adverse events such as liver or kidney acute disfunction or abnormalities in coagulation parameters during patients’ hospitalization and within 30 days after patients discharge. This is extremely important for patients with SCD, who should have access to multimodal therapy to control recurrent acute pain crisis in order to limit central sensitization a fearsome issue of undertreated recurrent acute pain and of chronic pain.
引用
收藏
相关论文
共 50 条
  • [1] Safety and efficacy of ketorolac continuous infusion for multimodal analgesia of vaso-occlusive crisis in patients with sickle cell disease
    Pinto, Valeria Maria
    Gianesin, Barbara
    Sardo, Salvatore
    Mazzi, Filippo
    Baiardi, Giammarco
    Menotti, Sofia
    Piras, Fabio
    Quintino, Sabrina
    Robello, Giacomo
    Mattioli, Francesca
    Finco, Gabriele
    Forni, Gian Luca
    De Franceschi, Lucia
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2024, 19 (01)
  • [2] Effect of ketorolac in pediatric sickle cell vaso-occlusive pain crisis
    Hardwick, WE
    Givens, TG
    Monroe, KW
    King, WD
    Lawley, D
    [J]. PEDIATRIC EMERGENCY CARE, 1999, 15 (03) : 179 - 182
  • [3] Ketorolac versus meperidine in vaso-occlusive crisis: A study of safety and efficacy
    Grisham, JE
    Vichinsky, EP
    [J]. INTERNATIONAL JOURNAL OF PEDIATRIC HEMATOLOGY/ONCOLOGY, 1996, 3 (04): : 239 - 247
  • [4] Benefits of Patient-Controlled Analgesia without Continuous Infusion for the Treatment of Sickle Cell Disease Vaso-Occlusive Crisis Pain
    Carullo, Veronica
    Murphy, Meagan
    Choi, Jaeun
    Gao, Qi
    Driscoll, Catherine
    Manwani, Deepa
    [J]. BLOOD, 2015, 126 (23)
  • [5] A randomised controlled trial of patient controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease
    Van Beers, EJ
    Nieuwkerk, PT
    Van Tuijn, CFJ
    Friederich, PW
    Levi, MM
    Vranken, JH
    Biemond, BJ
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2006, 133 : 120 - 120
  • [6] PATIENT-CONTROLLED ANALGESIA IN PATIENTS WITH SICKLE-CELL VASO-OCCLUSIVE CRISIS
    MCPHERSON, E
    PERLIN, E
    FINKE, H
    CASTRO, O
    PITTMAN, J
    [J]. AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1990, 299 (01): : 10 - 12
  • [7] A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis
    Dampier, Carlton D.
    Telen, Marilyn Jo
    Wun, Ted
    Brown, R. Clark
    Desai, Payal
    El Rassi, Fuad
    Fuh, Beng
    Kanter, Julie
    Pastore, Yves
    Rothman, Jennifer
    Taylor, James G.
    Readett, David
    Sivamurthy, Krupa M.
    Tammara, Brinda
    Tseng, Li-Jung
    Lozier, Jay Nelson
    Thackray, Helen
    Magnani, John L.
    Hassell, Kathryn L.
    [J]. BLOOD, 2023, 141 (02) : 168 - 179
  • [8] A multimodal pain protocol for treatment of vaso-occlusive crisis in patients with sickle cell disease: Implementation and evaluation
    Admiraal, Manouk
    van Daalen, Jonathan
    Ritt, Michael W. J.
    Dekker, Joost
    van Tuijn, Charlotte F. J.
    Nur, Erfan
    Hollmann, Markus W.
    Hermanns, Henning
    Hermanides, Jeroen
    Biemond, Bart J.
    [J]. EUROPEAN JOURNAL OF HAEMATOLOGY, 2023, 111 (03) : 382 - 390
  • [9] Approach to the vaso-occlusive crisis in adults with sickle cell disease
    Yale, SH
    Nagib, N
    Guthrie, T
    [J]. AMERICAN FAMILY PHYSICIAN, 2000, 61 (05) : 1349 - 1356
  • [10] Crizanlizumab in vaso-occlusive crisis caused by sickle cell disease
    Gardner, R., V
    [J]. DRUGS OF TODAY, 2020, 56 (11) : 705 - 714