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Feasibility of Outpatient Hybrid Brachytherapy for Cervical Cancer with Minimal Sedation: Results from a Single-institutional Protocol

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Date 2023 Mar 27
PMID 36970442
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Abstract

Purpose: Pain control techniques during high-dose-rate hybrid intracavitary-interstitial brachytherapy (HBT) for cervical cancer vary widely, with many centers opting for general anesthesia (GA) or conscious sedation (CS). Here, we describe a single-institutional series of patients treated with HBT and ASA-defined minimal sedation, utilizing oral analgesic and anxiolytic medications in substitution for GA or CS.

Material And Methods: The charts of patients who underwent HBT treatments for cervical cancer from June 2018 to May 2020 were retrospectively reviewed. Prior to HBT, all patients underwent an exam under anesthesia (EUA), and Smit sleeve placement under general anesthesia or deep sedation. Oral lorazepam and oxycodone/acetaminophen were administered between 30-90 minutes before HBT procedure for minimal sedation. HBT placement was performed on computed tomography (CT) table, with needle advancement under CT-guidance.

Results: Treatments with minimal sedation were attempted in 63 patients. A total of 244 interstitial implants with 453 needles were placed via CT-guidance. Sixty-one patients (96.8%) tolerated the procedure without any additional intervention, while two patients (3.2%) required the use of epidural anesthesia. None of the patients in the series required a transition to general anesthesia for the procedure. Bleeding, which resolved with short-term vaginal packing, occurred in 22.1% of insertions.

Conclusions: In our series, the treatment of HBT for cervical cancer with minimal sedation was feasible at a high percentage (96.8%). The ability to perform HBT without GA or CS could be a reasonable option to provide image-guided adaptive brachytherapy (IGABT) with limited resources, allowing for more widespread use. Further investigations using this technique are warranted.

References
1.
Rijkmans E, Nout R, Rutten I, Ketelaars M, Neelis K, Laman M . Improved survival of patients with cervical cancer treated with image-guided brachytherapy compared with conventional brachytherapy. Gynecol Oncol. 2014; 135(2):231-8. DOI: 10.1016/j.ygyno.2014.08.027. View

2.
Potter R, Tanderup K, Schmid M, Jurgenliemk-Schulz I, Haie-Meder C, Fokdal L . MRI-guided adaptive brachytherapy in locally advanced cervical cancer (EMBRACE-I): a multicentre prospective cohort study. Lancet Oncol. 2021; 22(4):538-547. DOI: 10.1016/S1470-2045(20)30753-1. View

3.
Kirchheiner K, Czajka-Pepl A, Ponocny-Seliger E, Scharbert G, Wetzel L, Nout R . Posttraumatic stress disorder after high-dose-rate brachytherapy for cervical cancer with 2 fractions in 1 application under spinal/epidural anesthesia: incidence and risk factors. Int J Radiat Oncol Biol Phys. 2014; 89(2):260-7. DOI: 10.1016/j.ijrobp.2014.02.018. View

4.
Nomden C, de Leeuw A, Moerland M, Roesink J, Tersteeg R, Jurgenliemk-Schulz I . Clinical use of the Utrecht applicator for combined intracavitary/interstitial brachytherapy treatment in locally advanced cervical cancer. Int J Radiat Oncol Biol Phys. 2011; 82(4):1424-30. DOI: 10.1016/j.ijrobp.2011.04.044. View

5.
Bates J, Thaker N, Parekh A, Royce T . Geographic access to brachytherapy services in the United States. Brachytherapy. 2021; 21(1):29-32. DOI: 10.1016/j.brachy.2021.05.004. View