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Updated: Dec 8, 2025

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How I Treat Acute and Persistent Sickle Cell Pain
1Cardeza Foundation for Hematologic Research, Department of Medicine, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA.
Sickle cell disease (SCD) pain management requires individualized approaches for acute vaso-occlusive crises (VOC). Understanding pain types and complications like opioid tolerance is crucial for effective patient care.
Area of Science:
- Hematology
- Pain Medicine
- Clinical Therapeutics
Background:
- Sickle cell disease (SCD) is characterized by significant pain, a major manifestation impacting patient quality of life.
- The classification and interrelationship of various pain types in SCD, including acute, chronic, and neuropathic pain, remain subjects of ongoing discussion.
- Effective management of SCD pain is essential, yet presents complex challenges.
Purpose of the Study:
- To review the general approach to managing acute vaso-occlusive crisis (VOC) pain in sickle cell disease.
- To present and discuss common management issues encountered in SCD patients, such as individualized pain treatment, opioid tolerance, and withdrawal syndromes.
- To highlight the distinction between resolving pain and persistent complications like tolerance and withdrawal.
Main Methods:
- Review of general strategies for acute vaso-occlusive crisis (VOC) pain management.
- Case-based discussion of five patients illustrating common challenges in SCD pain management.
- Description of clinical aspects and management of issues including individualized treatment, bilaterality of pain, illicit drug use, opioid tolerance, opioid-induced hyperalgesia, and withdrawal.
Main Results:
- Standard approaches to acute VOC pain include education, counseling, pharmacotherapy, non-pharmacotherapy, and fluid therapy.
- Common clinical issues in SCD pain management involve individualized treatment, pain bilaterality, illicit drug use, opioid tolerance, opioid-induced hyperalgesia, and withdrawal.
- Complications such as opioid tolerance and withdrawal can persist post-discharge, potentially misdiagnosed as chronic pain.
Conclusions:
- Individualized pain management strategies are paramount in sickle cell disease (SCD).
- Recognizing and addressing specific challenges like opioid tolerance and withdrawal is critical for effective long-term care.
- Differentiating between acute/relapsing pain and persistent complications is vital for appropriate treatment and patient outcomes.
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