Local Anesthesia With General Anesthesia for Pediatric Bone Marrow Procedures

Author:

Zarnegar-Lumley Sara12,Lange Katharine R.13,Mathias Melissa D.14,Nakajima-Hatano Miho15,Offer Katharine M.16,Ogu Ugochi O.17,Ortiz Michael V.1,Tan Kay See8,Kellick Michael9,Modak Shakeel1,Roberts Stephen S.1,Basu Ellen M.1,Dingeman R. Scott11011

Affiliation:

1. Departments of Pediatrics,

2. Division of Hematology/Oncology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee;

3. Children’s Minnesota Hematology Oncology, Minneapolis, Minnesotta;

4. Regeneron Pharmaceuticals, Tarrytown, New York;

5. National Cancer Center, Tokyo, Japan;

6. Children's Cancer Institute, Joseph M. Sanzari Children's Hospital, Hackensack University Medical Center, Hackensack, New Jersey;

7. Division of Hematology, Department of Oncology, Montefiore Medical Center, Bronx, New York; and

8. Epidemiology and Biostatistics,

9. Pharmacy, and

10. Anesthesiology and Critical Care Medicine, Memorial Sloan Kettering Cancer Center, New York, New York;

11. Division of Pediatric Anesthesiology, Department of Anesthesiology and Critical Care Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland

Abstract

BACKGROUND: Pediatric patients with cancer undergo repeated painful procedures, including bone marrow aspirations and biopsies (BMABs). Optimal management of procedure-related pain can reduce discomfort, anxiety, and distress. METHODS: Children with neuroblastoma were randomly assigned to 1 of 2 arms on a prospective, single-blind, crossover trial conducted at Memorial Sloan Kettering Cancer Center from October 2016 to January 2018 (www.clinicaltrials.gov, identifier NCT02924324). Participants underwent 2 sequential BMABs: one with general anesthesia (GA) alone, the other with GA plus local anesthesia (LA) (GA + LA). The objective was to assess procedure-related pain and its interference with quality of life (QoL) with GA versus GA + LA. Primary outcome was percentage of participants requiring postprocedural opioids. Secondary outcomes were total opioid and nonopioid analgesics, pain scores, time to first analgesic, QoL, and toxicity. Management of postprocedural pain was standardized. RESULTS: Of 56 participants randomly assigned (3–16.5 years old), 46 completed both procedures. There was no significant difference in percentage of participants requiring opioids with GA versus GA + LA (24% vs 20%, P = .5). Pain scores in the recovery room were significantly lower for GA + LA versus GA (median [IQR]: 0 [0–2] vs 2 [0–4], P = .002). There were no statistically significant differences in total opioid or nonopioid analgesic, 6- and 24-hour pain scores, median time to first analgesic, or pain interference. No adverse events occurred. CONCLUSIONS: LA was associated with significant improvement in pain scores in the immediate recovery period. LA did not reduce postprocedural opioid use, nor did it improve QoL for patients undergoing BMAB with GA.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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