Bridging the Gap Among Clinical Practice Guidelines for Pain Management in Cancer and Sickle Cell Disease

Author:

Schatz Alyssa A.1,Oliver Thomas K.2,Swarm Robert A.13,Paice Judith A.124,Darbari Deepika S.56,Dowell Deborah7,Meghani Salimah H.8,Winckworth-Prejsnar Katy1,Bruera Eduardo29,Plovnick Robert M.5,Richardson Lisa7,Vapiwala Neha8,Wollins Dana2,Hudis Clifford A.2,Carlson Robert W.1

Affiliation:

1. 1National Comprehensive Cancer Network, Plymouth Meeting, Pennsylvania;

2. 2American Society of Clinical Oncology, Alexandria, Virginia;

3. 3Washington University School of Medicine, St. Louis, Missouri;

4. 4Northwestern University, Feinberg School of Medicine, Chicago, Illinois;

5. 5American Society of Hematology, Washington, DC;

6. 6Children’s National Medical Center, George Washington University School of Medicine and Health Sciences, Washington, DC;

7. 7Centers for Disease Control and Prevention, Atlanta, Georgia;

8. 8University of Pennsylvania, Philadelphia, Pennsylvania; and

9. 9University of Texas MD Anderson Cancer Center, Houston, Texas.

Abstract

Opioids are a critical component of pain relief strategies for the management of patients with cancer and sickle cell disease. The escalation of opioid addiction and overdose in the United States has led to increased scrutiny of opioid prescribing practices. Multiple reports have revealed that regulatory and coverage policies, intended to curb inappropriate opioid use, have created significant barriers for many patients. The Centers for Disease Control and Prevention, National Comprehensive Cancer Network, and American Society of Clinical Oncology each publish clinical practice guidelines for the management of chronic pain. A recent JAMA Oncology article highlighted perceived variability in recommendations among these guidelines. In response, leadership from guideline organizations, government representatives, and authors of the original article met to discuss challenges and solutions. The meeting featured remarks by the Commissioner of Food and Drugs, presentations on each clinical practice guideline, an overview of the pain management needs of patients with sickle cell disease, an overview of perceived differences among guidelines, and a discussion of differences and commonalities among the guidelines. The meeting revealed that although each guideline varies in the intended patient population, target audience, and methodology, there is no disagreement among recommendations when applied to the appropriate patient and clinical situation. It was determined that clarification and education are needed regarding the intent, patient population, and scope of each clinical practice guideline, rather than harmonization of guideline recommendations. Clinical practice guidelines can serve as a resource for policymakers and payers to inform policy and coverage determinations.

Publisher

Harborside Press, LLC

Subject

Oncology

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