Severity, timeline, and management of complications after stereotactic brain biopsy

Author:

Riche Maximilien12,Marijon Pauline12,Amelot Aymeric1,Bielle Franck23,Mokhtari Karima23,Chambrun Marc Pineton de456,Joncour Alexandre Le7,Idbaih Ahmed28,Touat Mehdi28,Do Chung-Hi9,Deme Mamadou9,Pasqualotto Romain9,Jacquens Alice9,Degos Vincent91011,Shotar Eimad12,Chougar Lydia212,Carpentier Alexandre12,Mathon Bertrand12

Affiliation:

1. Departments of Neurosurgery,

2. INSERM U 1127, CNRS UMR 7225, Sorbonne University, UMR S 1127, Paris Brain Institute, ICM

3. Neuropathology,

4. Internal Medicine 2,

5. Intensive Care Medicine,

6. INSERM, UMRS_1166-ICAN, Institute of Cardiometabolism and Nutrition

7. Internal Medicine and Clinical Immunology,

8. Neurology Mazarin,

9. Anesthesia, Critical Care, and Perioperative Medicine, and

10. Clinical Research Group ARPE, Sorbonne University

11. INSERM UMR 1141, PROTECT, Paris, France

12. Neuroradiology, APHP, Sorbonne University, La Pitié-Salpêtrière Hospital

Abstract

OBJECTIVE The literature shows discrepancies in stereotactic brain biopsy complication rates, severities, and outcomes. Little is known about the timeline of postbiopsy complications. This study aimed to analyze 1) complications following brain biopsies, using a graded severity scale, and 2) a timeline of complication occurrence. The secondary objectives were to determine factors associated with an increased risk of complications and to assess complication-related management and extra costs. METHODS The authors retrospectively examined 1500 consecutive stereotactic brain biopsies performed in adult patients at their tertiary medical center between April 2009 and April 2019. RESULTS Three hundred eighty-one biopsies (25.4%) were followed by a complication, including 88.2% of asymptomatic hemorrhages. Symptomatic complications involved 3.0% of the biopsies, and 0.8% of the biopsies were fatal. The severity grading scale had a 97.6% interobserver reproducibility. Twenty-three (51.1%) of the 45 symptomatic complications occurred within the 1st hour following the biopsy, while 75.6% occurred within the first 6 hours. Age ≥ 65 years, second biopsy procedures, gadolinium-enhanced lesions, glioblastomas, and lymphomas were predictors of biopsy-related complications. Brainstem biopsy-targeted lesions and cerebral toxoplasmosis were predictive of mortality. Asymptomatic hemorrhage was associated with delayed (> 6 hours) symptomatic complications. Symptomatic complications led to extended hospitalization in 86.7% of patients. The average extra cost for management of a patient with postbiopsy symptomatic complication was $35,702. CONCLUSIONS Symptomatic complications from brain biopsies are infrequent but associated with substantial adverse effects and cost implications for the healthcare system. The use of a severity grading scale, as the authors propose in this article, helps to classify complications according to the therapeutic consequences and the patient’s outcome. Because this study indicates that most complications occur within the first few hours following the biopsy, postbiopsy monitoring can be tailored accordingly. The authors therefore recommend systematic monitoring for 2 hours in the recovery unit and a CT scan 2 hours after the end of the biopsy procedure. In addition, they propose a modern algorithm for optimal postoperative management of patients undergoing stereotactic biopsy.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Genetics,Animal Science and Zoology

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