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Published on: August 1, 2018
[Anesthesia for cesarean section in a patient with familiar hypertrophic cardiomyopathy: case report.]
Renato Mestriner Stocche1, Luis Vicente Garcia, Jyrson Guilherme Klamt
1Serviço de Anestesiologia, HC, FMRP, USP.
Insights
Anesthetic management for cesarean section in patients with Familiar Hypertrophic Cardiomyopathy (FHC) can safely utilize combined spinal-epidural anesthesia. This technique, with careful monitoring and vasopressor use, avoids complications in high-risk pregnancies.
Area of Science:
- Cardiology
- Anesthesiology
- Genetics
Context:
- Familiar Hypertrophic Cardiomyopathy (FHC) is a rare genetic cardiac condition.
- FHC can lead to left ventricular outlet obstruction, arrhythmias, and ischemia.
- Cesarean sections in FHC patients require careful anesthetic considerations.
Purpose:
- To report the anesthetic management of a cesarean section in a pregnant patient with FHC.
- To evaluate the safety and efficacy of combined spinal-epidural anesthesia in this context.
Summary:
- A pregnant patient with FHC and a history of ventricular tachycardia underwent an elective cesarean section.
- Combined spinal-epidural anesthesia was administered with careful hemodynamic monitoring and vasopressor support.
- The procedure was completed without perioperative hypotension or maternal complications.
Impact:
- Combined spinal-epidural anesthesia is a safe alternative to general anesthesia for cesarean sections in FHC patients.
- This approach can help avoid increased myocardial contractility and manage hypotension effectively.
- Highlights the importance of tailored anesthetic strategies for high-risk obstetric patients.
Background And Objectives:
Familiar Hypertrophic cardiomyopathy (FHC) is a rare hereditary cardiac disorder characterized by hypertrophy of the ventricular septum and variable degrees of subvalvular aortic stenosis. In this disease, the increase in myocardial contractility and reduction in peripheral vascular resistance can aggravate left ventricular outlet obstruction, leading to arrhythmias and cardiac ischemia. The objective of this report was to discuss the anesthetic management of cesarean section in a patient with FHC.
Case Report:
A patient in the 33rd week of pregnancy and prior diagnosis of FHC presented, on the 24-hour Holter monitor, 22 episodes of non-sustained ventricular tachycardia (NSVT) and 2 episodes of sustained ventricular tachycardia (SVT). She complained of episodes of palpitation, dyspnea, and chest pain of short duration. The patient was medicated with atenolol, with control of symptoms and cardiac arrhythmias. Within 38 weeks and 5 days of gestation, the patient underwent elective cesarean section. Besides the usual monitoring, analysis of the ST segment and invasive blood pressure were also instituted. Anesthesia consisted of combined spinal-epidural technique with subarachnoidal administration of 5 microg of sufentanil followed by the administration of increasing doses of 0.375% bupivacaine until it reached the level of T6 (total of 16 mL). Metaraminol was used as a vasopressor. Perioperative maternal hypotension or other complications were not observed.
Conclusions:
General anesthesia is often used for cesarean sections in patients with FHC. Spinal-epidural anesthesia with slow installation of the blockade was a safe alternative. In those patients, one should avoid an increase in myocardial contractility and, if necessary, a a-agonist should be used to treat maternal hypotension.
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