Use of Dexmedetomidine in a Parturient with Multiple Endocrine Neoplasia Type 2A Undergoing Adrenalectomy and Thyroidectomy

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Use of Dexmedetomidine in a Parturient with Multiple Endocrine Neoplasia Type 2A Undergoing Adrenalectomy and Thyroidectomy PRACTICE CASE REPORT Use of Dexmedetomidine in a Parturient With Multiple Endocrine Neoplasia Type 2A Undergoing Adrenalectomy and Thyroidectomy: A Case Report Amanda L. Faulkner, MD, Eric Swanson, MD, Thomas L. McLarney, MD, Cortney Y. Lee, MD, and Annette Rebel, MD * * * † * 08/15/2018 on BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AWnYQp/IlQrHD3yRlXg5VZA8uqNuqWFo8dRhJiNZRTFLkCeIa0nEMHM2KbYm37VRaE3A== by https://journals.lww.com/aacr from Downloaded Dexmedetomidine is a selective α2-agonist, frequently used in perioperative medicine as anes- thesia adjunct. The medication carries a Food and Drug Administration pregnancy category C Downloaded designation and is therefore rarely used for parturients undergoing nonobstetric surgery. We are reporting the use of dexmedetomidine in the anesthetic management of a parturient undergoing minimally invasive unilateral adrenalectomy for pheochromocytoma during the second trimester from https://journals.lww.com/aacr of pregnancy. Additionally, because of the multiple endocrine neoplasia type 2A constellation with diagnosis of medullary thyroid cancer, the patient underwent a total thyroidectomy 1 week after the adrenalectomy. (A&A Practice. XXX;XXX:00–00.) exmedetomidine is a selective α2-agonist, fre- CASE REPORT by BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AWnYQp/IlQrHD3yRlXg5VZA8uqNuqWFo8dRhJiNZRTFLkCeIa0nEMHM2KbYm37VRaE3A== quently used in perioperative medicine. It has A 34-year-old gravida 3 para 2 woman (body weight, 61 Dfound favor in this setting because of its sedative kg; body height, 167 cm) at 18 weeks’ gestation presented and analgesic properties without associated respiratory to her obstetrician and was found to have a single coin- depression. Current evidence shows that perioperative dex- sized neck mass on physical examination. Medullary thy- medetomidine is associated with reduced opioid require- roid carcinoma was diagnosed by fne needle aspiration. ments, reduced emergence delirium, decreased incidence of Investigational thyroid studies revealed a low-normal postoperative nausea and vomiting, reduced incidence of thyroid-stimulating hormone level, an elevated calcitonin postoperative shivering, and increased hemodynamic sta- level, and an elevated carcinoembryonic antigen value bility when compared to other anesthetic agents.1 (Table). Further laboratory evaluation revealed signif- In the United States, dexmedetomidine carries a Food cantly elevated fractionated metanephrines, confrming and Drug Administration (FDA) pregnancy category C des- the diagnosis of pheochromocytoma. The patient denied ignation, indicating that insuffcient data exist to document palpitations, sweating, or headaches. A magnetic resonance the agent’s effect on the fetus and that potential benefts imaging of the abdomen demonstrated a 3-cm left adrenal may warrant drug use during pregnancy despite poten- mass concerning for pheochromocytoma (Figure 1) and a tial risks.2 Dexmedetomidine has been successfully used as contralateral 1 cm adrenal nodule. On these diagnoses of an adjunct for both labor analgesia and cesarean delivery.3 thyroid carcinoma and pheochromocytoma, the patient However, information regarding the use of perioperative admitted to a family history of MEN2A. Her sister was dexmedetomidine for nonobstetric surgery during preg- diagnosed with a gene mutation that is associated with nancy is sparse.4–6 MEN2A and MEN type 2B and had a history of metastatic We are reporting the use of dexmedetomidine in the medullary thyroid carcinoma and underwent bilateral anesthetic management of a parturient undergoing mini- adrenalectomies for pheochromocytoma. Her mother was mally invasive unilateral adrenalectomy for pheochro- diagnosed with medullary thyroid carcinoma on autopsy. mocytoma during the second trimester of pregnancy. Interestingly, our patient refused genetic testing approxi- Additionally, because of the multiple endocrine neoplasia mately 3 years before her presentation (at the time of her type 2A (MEN2A) constellation including diagnoses of both sister’s diagnosis). pheochromocytoma and medullary thyroid carcinoma,7 the on 08/15/2018 patient underwent a total thyroidectomy with neck dissec- Preoperative Management tion, using a similar anesthetic approach 1 week after the Although the patient did not report signifcant symptoms adrenalectomy. related to the pheochromocytoma, the patient care team The patient provided written consent to use her informa- (endocrinologist, oncologist, and surgeon) felt that the tion for publication. pheochromocytoma should be resected before the thyroid mass, and the thyroid malignancy be addressed as soon as From the Departments of Anesthesiology and Surgery, University of Ken- possible (before delivery). The aim was to complete all pro- tucky, Lexington, Kentucky. cedures within the second trimester. An organized care plan * † Accepted for publication July 3, 2018. was created by obstetric, surgical, and anesthesia providers; Funding: None. the plan detailed a minimally invasive adrenalectomy at 22 The authors declare no conficts of interest. weeks gestational age, followed by a total thyroidectomy Address correspondence to Annette Rebel, MD, Department of Anesthesiology, approximately 1 week later. Therefore, the workup and University of Kentucky, 800 Rose St, N 202 Lexington, KY 40536. Address e-mail to [email protected]. time for hemodynamic optimization were signifcantly lim- Copyright © 2018 International Anesthesia Research Society ited. A transthoracic echocardiogram was performed and DOI: 10.1213/XAA.0000000000000861 demonstrated normal cardiac anatomy and unremarkable XXX XXX, 2018 • Volume XXX • Number XXX cases-anesthesia-analgesia.org 1 Copyright © 2018 International Anesthesia Research Society. Unauthorized reproduction of this article is prohibited. Table. Preoperative Laboratory Evaluation Therefore, only the large adrenal nodule was addressed at Thyroid Nodule Workup this stage to avoid the hormone replacement requirements Patient Value Normal Range warranted by a bilateral adrenalectomy during the preg- TSH 0.98 0.4–4.2 μIU/mL nancy. The patient remained on phenoxybenzamine (lower Calcitonin 264 <5 pg/mL doses) through the second thyroid surgery as a precaution. CEA 96 <4 ng/mL It was successfully discontinued after the thyroid surgery. FNA Medullary thyroid carcinoma, positive for all the submitted neuroendocrine markers Anesthetic Management for Posterior Free metanephrine 2.1 <0.9 nmol/L Free normetanephrine 3.3 <0.9 nmol/L Retroperitoneoscopic Adrenalectomy Preoperatively, the patient arrived anxious regarding her The Table describes the parturient’s initial workup on discovery of the neck mass. The calcitonin and CEA levels were concerning for thyroid carcinoma, pending surgeries. The patient requested anxiolytic med- which was confrmed by FNA. Elevated metanephrines and normetanephrines ications before being taken to the operating room. After raised suspicion for pheochromocytoma. a detailed discussion of risks and possible implication Abbreviations: CEA, carcinoembryonic antigen; FNA, fne needle aspiration; TSH, thyroid-stimulating hormone. on the pregnancy, we initiated a dexmedetomidine load (0.5 μg/kg over 15 minutes) and infusion (0.5 μg/kg/h) in the preoperative area under continuous HR and pulse oximetry monitoring. Once in the operating suite, a pre- induction arterial line was inserted. After an intrave- nous induction of anesthesia (fentanyl, 100 μg; propofol, 100 mg; rocuronium, 60 mg) in modifed rapid sequence fashion, a central venous catheter was placed in the right internal jugular vein. The patient positioning is shown in Figure 2. This position was chosen by the surgical team to allow best retroperitoneal exposure with minimal dis- turbance of the abdominal cavity. The posterior retroperi- toneal approach avoids the surgical manipulations of any intraabdominal organs and is usually faster than the trans- abdominal technique. Bispectral index monitoring was used for the assessment of anesthetic depth (range, 40–50). General anesthesia was maintained with isofurane (end- tidal concentration, 0.5–0.9 vol %); nicardipine and dex- medetomidine infusions were titrated for hemodynamic variations associated with tumor manipulation (target: Figure 1. Preoperative MRI, identifying nodule in left adrenal gland. mean arterial blood pressure [MAP] within 15% of base- The fgure demonstrates a nodule in the left adrenal gland (red line, HR within 90–110 bpm). Intravenous fentanyl boluses arrow). MRI, magnetic resonance imaging. (50–75 μg) were given intraoperatively (total 300 μg). The surgical procedure was completed in 109 minutes, cardiac function. The baseline blood pressure in the obste- and the total anesthetic exposure was 135 minutes. The trician offce was 140/98, and heart rate (HR) 96 beats per combination of dexmedetomidine, nicardipine, and bal- minute (bpm). Alpha blockade was initiated 2 weeks before anced general anesthesia provided stable hemodynamics the adrenalectomy using phenoxybenzamine. Blood pres- during adrenalectomy without severe hypertension or sure measurements fuctuated in the range of 121/80 to hypotension. There was no need for vasopressor therapy 108/67, and HR range 108–90 bpm without endorsement after tumor removal. The patient was extubated in the of orthostasis. Further symptomatic management and con- operating room at the end of the case. Postoperative fetal trol of hypertension thereafter were achieved with labetalol. HR (FHR) monitoring in the recovery room showed
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