Pain Relief in the Sickle-Cell Crisis: Intravenous Morphine Versus Ketorolac; A Double-Blind, Randomized Clinical Trial

Morteza Talebi Doluee; Behrang Rezvani Kakhki; Hamid Heidarian Mir; Mahsa Fateminayyeri; Farideh Madanitorbati; Somayyehalsadat Hosseini

Volume 21, Issue 4 , 2019, Pages 1-5

Abstract
  Background: Sickle cell disease (SCD) is a congenital hemoglobinopathy. A low Hb level and high hemoglobin-to-hematocrit ratio may lead to the vaso-occlusive crisis in patients, for the management of which hyperbaric oxygen, hydration, and pain relief therapy are proposed.Objectives: In this study, we ...  Read More