- Case report
- Open access
- Published:
Profound postinduction hypotension precipitated by immune checkpoint inhibitors: a case report
Journal of Medical Case Reports volume 18, Article number: 146 (2024)
Abstract
Background
With the increasing use of immune checkpoint inhibitors (ICIs) in cancer therapy, perioperative healthcare professionals need to be vigilant about potential immune-related adverse events (irAEs). We report a case of severe postinduction hypotension in a patient undergoing laparotomy due to suspected intraabdominal bleeding from gastric cancer and Krukenberg tumors, caused by unrecognized hypothyroidism precipitated by ICIs.
Case presentation
A 65-year-old Chinese female with a history of gastric adenocarcinoma and Krukenberg tumors, previously treated with nivolumab, presented to the emergency room with abdominal pain and hypotension. Despite ruling out other causes, including hypovolemia and anaphylaxis, her hypotension persisted. The patient was found to have severe hypothyroidism, likely an irAE from the use of nivolumab. Thyroxine replacement therapy resolved the hypotension, and the patient recovered uneventfully after surgery.
Conclusions
This case underscores the importance of considering irAEs, such as hypothyroidism, in patients treated with ICIs. Perioperative healthcare providers must remain vigilant for potential complications and promptly recognize and manage irAEs to optimize patient outcomes.
Background
While immune checkpoint inhibitor (ICI) therapy has improved patient outcomes, it has also led to an increase in unique immune-related adverse events (irAEs) [1, 2]. Endocrinopathies caused by ICIs have been reported in up to 5% of patients, with hypothyroidism occurring in up to 8% of patients [3]. Anesthesia in the presence of hypothyroidism carries an increased risk of morbidity and potential mortality [4, 5]. It is crucial to stay updated on the field of immunotherapy and its associated toxicities, which can complicate perioperative management [6, 7]. Herein, we report a case of severe postinduction hypotension in a female patient scheduled for laparotomy due to suspected intraabdominal bleeding due to gastric cancer and Krukenberg tumors. Her hypotension was later found to be caused by unrecognized hypothyroidism due to immune-related adverse events (irAEs) related to nivolumab.
Case presentation
A 65-year-old Chinese female presented to the emergency room (ER) with abdominal pain and one episode of syncope due to hypotension (70/60Â mmHg).
Upon physical examination for the current emergency room visit, a palpable mass was identified in the lower abdominal and pelvic region, accompanied by tenderness and rebound pain. Neurological exam is insignificant with E3V4M5. The patient’s vital signs were stable, with blood pressure (BP) of 90/60 mmHg, oxygen saturation (SPO2) of 91% on room air, heart rate (HR) of 64 bpm with normal electrocardiograph, and arterial blood gas (ABG) analysis showing a lactate (Lac) level of 3.5 mmol/L.
Laboratory results revealed a platelet level of 93 × 109/L, hemoglobin (Hb) of 101 g/L, hematocrit (Hct) of 28.7% and creatine kinase (CK) level of 1928 U/L with other liver and renal function tests, urinalysis and complete blood count tests within normal ranges.
An abdominal/pelvic computed tomography (CT) scan suggested possible bleeding in the uterine and appendix regions (Fig. 1). The patient's past medical history was significant for diagnosis of poorly differentiated adenocarcinoma in the gastric antrum 2 years ago, with initial tumor staging of cT4aN + . Following 3 cycles of FOLFOX treatment, Stable Disease (SD) was observed. Upon follow up newly identified seeding metastasis in the bilateral adnexal area led to a diagnosis of Progressive Disease (PD) with Krukenberg tumors. Then patient underwent 6 cycles of Nivolumab + XELOX with SD and tumor shrinkage achieved. Three months before the recent emergency visit, the patient had been on maintenance therapy with nivolumab + Capecitabine. During the treatment patients experienced iron-deficient anemia and one episode of upper gastrointestinal bleeding which completely resolved. There was no prior history of surgical procedures.
Peritoneocentesis performed in the ER revealed unclotted blood, indicating the need for emergency laparotomy. The patient's vital signs remained stable during her stay in the emergency room, with systolic BP ranging from 110 to 100 mmHg and HR ranging from 60 to 70 bpm. Her elevated CK was considered to be dermatomyositis caused by nivolumab, and methylprednisolone 40Â mg iv every 24Â h was given. Upon entering the operating room (OR), the patient was oriented, alert, and conscious (Glasgow Coma Scale: E4V5M6), with vitals similar to those in the ER and SPO2 at room air ranging from 85 to 88%. ABG analysis showed a pH of 7.43, Hct of 27.8%, Hb of 89 g/L, partial pressure of oxygen (PO2) of 72.9Â mmHg, partial pressure of carbon dioxide (PCO2) of 32.6Â mmHg, and lactate (Lac) of 4.7Â mmol/L. Invasive arterial blood pressure monitoring was initiated, and point-of-care ultrasonography (POCUS) was performed.
The transthoracic echocardiogram (TTE) showed normal left ventricular contractility with no obvious valvular abnormalities or RWMA. The inferior vena cava (IVC) was not collapsed, and respiratory variability was not apparent. Abdominal ultrasound showed her bilateral diaphragm elevated to around the T4 level, likely due to the abdominal mass and possible bleeding. Fluid was observed in both the left and right abdominal cavities. Pulmonary ultrasound revealed B-lines in the lower lung regions, possibly caused by the elevated diaphragm due to the abdominal mass and potential intraperitoneal bleeding.
During the POCUS exam, the patient remained calm and cooperative, showing no signs of distress. Due to elevated intraperitoneal pressure, rapid sequence induction was performed to minimize the risk of aspiration. Propofol Targeted control infusion of 3 µg/mL, rocuronium 50 µg, and fentanyl 50 µg were used for anesthesia induction, and the Sellick maneuver was performed. Successful intubation was quickly achieved, but the patient's blood pressure started to drop. Boluses of 6 mg ephedrine and 100 µg phenylephrine were administered. The patient was quickly placed in the Trendelenburg position to compensate for vasodilation and facilitate central venous catheter placement. Despite repeated doses of ephedrine (36mg in total) and phenylephrine (1mg in total), the patient remained hypotensive at approximately 60/40 mmHg and unresponsive to fluid resuscitation(rapid infusion of 500ml lactate ringer’s solution). A bolus of 20 µg of epinephrine was administered together with epinephrine infusion and norepinephrine infusion, gradually improving the patient's BP. Throughout the hypotensive period, which lasted approximately 15 min, the patient's heart rate remained below 80 bpm. After establishing a central line and initiating a continuous infusion of epinephrine and norepinephrine, the hypotension was slowly corrected, and the patient’s invasive BP stabilized at 130/70 mmHg with an epinephrine infusion rate of 0.15 µg/kg/min and a norepinephrine infusion rate of 0.1 µg/kg/min. Surgery revealed hemorrhagic infarction of the Krukenberg tumor due to torsion of the pedicle as the source of intra-abdominal bleeding. The patient received 4 units of packed red blood cells. ABG analysis at the end of the surgery showed an Hb level of 9 g/L and lactate of 8.2 mmol/L, with an Hct of 27.6%.
The surgery proceeded uneventfully and lasted approximately 90 min. Despite the absence of continuous surgical bleeding, vasopressor support could not be downscaled. The patient was transferred to the intensive care unit (ICU) with continuous vasopressor infusion. Bedside ultrasonography was repeated to investigate the cause of severe hypotension after the induction agent. The patient's ventricular contractility was normal, without other apparent signs of valvular abnormalities or RWMA. The possibility of an anaphylactic reaction to induction agents was considered. However, the patient’s absence of signs and symptoms of anaphylaxis, including cutaneous and respiratory manifestations, led us to consider another possible cause: an immune-related adverse event (irAE). Considering the patient's history of taking nivolumab, a PD-1 inhibitor, together with the patient's unelevated HR during intro-abdominal bleeding and profound hypotension after induction, thyroid dysfunction was suspected. Thyroid hormone levels were ordered together with cardiac biomarkers to detect cardiac injury. The results on the second day revealed severe hypothyroidism, while troponins and NT-pro BNP remained unelevated (Table 1). An endocrinology consult was ordered, and thyroxine was promptly administered. The patient was free of vasopressors and successfully weaned off ventilation after 14 h in the ICU and transferred to the ward on the 2nd postoperative day, with an uneventful recovery. Up to 6 months after the surgery, patient recovered well and underwent regular oncologic outpatient clinic visits.
Discussion
This case underscores the significance of recognizing and addressing post-induction hypotension, which, in our case, could have been prevented or at least mitigated if we had known about the patient's immune-related adverse event (irAE)-related hypothyroidism due to Nivolumab, a PD-1 inhibitor.
In contemporary surgical settings, it's uncommon to encounter patients with severe hypothyroidism undergoing elective surgeries [8]. Hypothyroidism can lead to heightened sensitivity to anesthetic agents during general anesthesia [9], along with reduced medication metabolism, bradycardia, and difficulties in weaning off mechanical ventilatory support [10]. Most reported complications have occurred in patients with unrecognized hypothyroidism [11]. Refractory hypotension and cardiogenic shock due to hypothyroidism can be corrected by levothyroxine in a few days [10, 12]. Therefore preoperative recognition of hypothyroidism is essential for the safe anesthetic management of these patients.
Reflecting on this case, the bradycardia resulting from hypothyroidism also masked relative hypovolemia state due to Krukenberg tumor infraction. Hypothyroidism can blunt sympatho-excitatory and tachycardic responses to decreases in blood pressure [13]. Poor end vital organ perfusion resulting in elevated lactate level can also be found among with sever hypothyroidism [12], consistent with patient’s preoperative elevated lactate level though her vitals seems to be stable with BP ranging from 110 to 100 mmHg and HR ranging from 60 to 70 bpm. The blunted response to initial bolus of phenylephrine and ephedrine can also be supported by research evidence indicating diminished sensitivity to alpha-adrenergic agonist in hypothyroid patients [14].
This case also underscores the value of bedside ultrasound, which can help rule out hypovolemia and contractility dysfunction related to ischemic heart problems or valvular dysfunction, leading us to consider other uncommon cause of hypotension and pining the culprit of (irAE)-related hypothyroidism.
In the future for all the patients having history of taking PD-1, a quick preoperative work-up of irAE is need for emergency and elective surgeries alike and guidance on levothyroxine in dose, route of administration, and loading dose s needed. The current American Thyroid Association (ATA) guidelines recommend intravenous administration of levothyroxine at an initial dose of 200–400 µg. However, treatment should be pragmatic and adapted to the patient’s age, medical history, and critical illness condition.
Conclusions
In emergent settings where time is limited to gather complete patient information, it is important to remain open-minded to the possibility of irAEs when treating patients receiving ICIs. This case also highlights the importance of POCUS in the initial diagnostic work-up of hepatic and renal complications, as in the present case. As the use of immune checkpoint inhibitors continues to expand, it is crucial for perioperative healthcare professionals to be aware of potential irAEs.
Availability of data and materials
Not applicable.
Abbreviations
- irAE:
-
Immune-related adverse event
- ICI:
-
Immune checkpoint inhibitor
- ECG:
-
Electrocardiogram
- T3:
-
Triiodothyronine
- T4:
-
Thyroxine
- FT4:
-
Free thyroxine
- FT3:
-
Free triiodothyronine
- TSH:
-
Thyroid-stimulating hormone
- A-TPO:
-
Anti-thyroid peroxidase antibodies
- A-Tg:
-
Anti-Thyroglobulin Antibodies
- TTE:
-
Transthoracic echocardiogram
- RWMA:
-
Regional wall motion abnormality
- ABG:
-
Arterial blood gas
- BP:
-
Blood pressure
- SPO2:
-
Oxygen saturation
- Hb:
-
Hemoglobin
- CK:
-
Creatine kinase
- POCUS:
-
Point-of-care ultrasonography
References
Wright JJ, Powers AC, Johnson DB. Endocrine toxicities of immune checkpoint inhibitors. Nat Rev Endocrinol. 2021;17(7):389–99. https://doi.org/10.1038/s41574-021-00484-3.
Iyer PC, Cabanillas ME, Waguespack SG, Hu MI, Thosani S, Lavis VR, et al. Immune-related thyroiditis with immune checkpoint inhibitors. Thyroid. 2018;28(10):1243–51. https://doi.org/10.1089/thy.2018.0116.
Khoja L, Day D, Wei-Wu Chen T, Siu LL, Hansen AR. Tumour- and class-specific patterns of immune-related adverse events of immune checkpoint inhibitors: a systematic review. Ann Oncol. 2017;28(10):2377–85. https://doi.org/10.1093/annonc/mdx286.
Murkin JM. Anesthesia and hypothyroidism: a review of thyroxine physiology, pharmacology, and anesthetic implications. Anesth Analg. 1982;61(4):371–83.
Ladenson PW, Levin AA, Ridgway EC, Daniels GH. Complications of surgery in hypothyroid patients. Am J Med. 1984;77(2):261–6. https://doi.org/10.1016/0002-9343(84)90701-0.
Spain L, Diem S, Larkin J. Management of toxicities of immune checkpoint inhibitors. Cancer Treat Rev. 2016;44:51–60. https://doi.org/10.1016/j.ctrv.2016.02.001.
Darnell EP, Mooradian MJ, Baruch EN, Yilmaz M, Reynolds KL. Immune-related adverse events (irAEs): diagnosis, management, and clinical pearls. Curr Oncol Rep. 2020;22(4):39. https://doi.org/10.1007/s11912-020-0897-9.
Bogojevic M, Bansal V, Pattan V, Singh R, Tekin A, Sharma M, et al. Association of hypothyroidism with outcomes in hospitalized adults with COVID-19: results from the International SCCM Discovery Viral Infection and Respiratory Illness Universal Study (VIRUS): COVID-19 Registry. Clin Endocrinol (Oxf). 2022. https://doi.org/10.1111/cen.14699.
Kim JM, Hackman L. Anesthesia for untreated hypothyroidism: report of three cases. Anesth Analg. 1977;56(2):299–302.
Kumar E, McCurdy MT, Koch CA, Hamadah A, Fülöp T, Gharaibeh KA. Impairment of thyroid function in critically ill patients in the intensive care units. Am J Med Sci. 2018;355(3):281–5. https://doi.org/10.1016/j.amjms.2017.06.026.
Weinberg AD, Brennan MD, Gorman CA, Marsh HM, O’Fallon WM. Outcome of anesthesia and surgery in hypothyroid patients. Arch Intern Med. 1983;143(5):893–7.
Bourcier S, Coutrot M, Ferré A, Van Grunderbeeck N, Charpentier J, Hraiech S, et al. Critically ill severe hypothyroidism: a retrospective multicenter cohort study. Ann Intensive Care. 2023;13(1):15. https://doi.org/10.1186/s13613-023-01112-1.
Foley CM, McAllister RM, Hasser EM. Thyroid status influences baroreflex function and autonomic contributions to arterial pressure and heart rate. Am J Physiol Heart Circ Physiol. 2001;280(5):H2061–8. https://doi.org/10.1152/ajpheart.2001.280.5.H2061.
Polikar R, Kennedy B, Ziegler M, Smith J, Nicod P. Decreased sensitivity to alpha-adrenergic stimulation in hypothyroid patients. J Clin Endocrinol Metab. 1990;70(6):1761–4. https://doi.org/10.1210/jcem-70-6-1761.
Acknowledgements
Not applicable.
Funding
CAMS Innovation Fund for Medical Sciences(2021-I2M-C&T-B-020).
Author information
Authors and Affiliations
Contributions
LC and AFZ drafted the manuscript; CHY and WC edited and approved the final version of the manuscript. All authors are involved with the clinical management of this case.
Corresponding author
Ethics declarations
Ethical approval and consent to participate
Written informed consent was obtained from the patient for publication of this case report.
Consent for publication
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Competing interests
The authors declare that they have no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Che, L., Zhu, A., Chen, W. et al. Profound postinduction hypotension precipitated by immune checkpoint inhibitors: a case report. J Med Case Reports 18, 146 (2024). https://doi.org/10.1186/s13256-024-04375-9
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s13256-024-04375-9