The Evaluation of Patient‐Controlled Analgesia Compared to Standard Opioid Analgesic Therapy in Pain Management Among Patients With Sickle Cell Disease: A Systematic Review and Meta‐Analysis Protocol

ABSTRACT Background and Aims Sickle cell disease (SCD) is an inherited blood disorder characterized by the production of abnormal hemoglobin S (HbS), leading to the deformation of red blood cells into a sickle shape under low oxygen conditions. These deformed cells impede blood flow, causing vaso‐oc...

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Main Authors: Maria Pramila D'Costa, Melita Sheela Alva, Seyed Aria Nejadghaderi, Salha Humaid Al Bloushi, Wafa Ibrahim Saleh Al Shizawi, Nikhil Muduli, Sana Ahuja, Salma Al‐Amri, Alireza Mosavi Jarrahi, Nabeel Al‐Yateem, Syed Azizur Rahman, Amina Mohammed Al‐Marzouqi
Format: Article
Language:English
Published: Wiley 2025-03-01
Series:Health Science Reports
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Online Access:https://doi.org/10.1002/hsr2.70577
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