# Use of Intravenous Clevidipine in the Management of Severe Preeclampsia: A Case Report

**Authors:** Cody Brazeal, Anne Shapiro

PMC · DOI: 10.7759/cureus.99287 · Cureus · 2025-12-15

## TL;DR

This case report describes the successful use of clevidipine, an intravenous drug, to manage severe preeclampsia when standard treatments failed.

## Contribution

The paper presents a novel case of clevidipine use in obstetric hypertensive emergencies, emphasizing its advantages in titratable blood pressure control.

## Key findings

- Clevidipine effectively controlled blood pressure in a patient with severe preeclampsia unresponsive to standard therapy.
- Its rapid onset and short half-life allow precise and flexible blood pressure management during critical obstetric procedures.
- Clevidipine's metabolism via esterases avoids reliance on impaired hepatic or renal function common in preeclampsia.

## Abstract

Severe preeclampsia is a hypertensive disorder of pregnancy that poses significant risks to both maternal and fetal health. First-line antihypertensives such as labetalol, hydralazine, and nifedipine are widely used; however, alternative agents may be considered in refractory cases. Clevidipine, an ultrashort-acting intravenous dihydropyridine calcium channel blocker, offers rapid titratability and is used in critical care settings, although its use in pregnancy remains understudied. We present a case of successful clevidipine use in a patient with severe preeclampsia refractory to standard therapy, highlighting its potential role in obstetric hypertensive emergencies. Clevidipine was selected due to its rapid onset, short half-life, and capacity for precise, titratable blood pressure control. Additionally, its metabolism by blood and tissue esterases, independent of hepatic or renal function, makes clevidipine advantageous in preeclampsia, where hepatic and renal dysfunction are often part of the disease process. Its rapid titratability also allows prompt discontinuation following spinal anesthesia, preventing prolonged hypotension that may result from non-titratable agents.

## Linked entities

- **Chemicals:** Clevidipine (PubChem CID 153994), labetalol (PubChem CID 3869), hydralazine (PubChem CID 3637), nifedipine (PubChem CID 4485)
- **Diseases:** preeclampsia (MONDO:0005081)

## Full-text entities

- **Diseases:** hepatic and renal dysfunction (MESH:D008107), Preeclampsia (MESH:D011225), hypotension (MESH:D007022), hypertensive disorder (MESH:D006973)
- **Chemicals:** dihydropyridine (MESH:C038806), Clevidipine (MESH:C118563), labetalol (MESH:D007741), hydralazine (MESH:D006830), nifedipine (MESH:D009543)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12802805/full.md

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Source: https://tomesphere.com/paper/PMC12802805