Malignant hypertension: diagnosis, treatment and prognosis with experience from the Bordeaux cohort

Sébastien Rubin1, Antoine Cremer2, Romain Boulestreau2

  • 1Service de Néphrologie, Transplantation, Dialyse et Aphérèses, Hôpital Pellegrin.

Journal of Hypertension
|August 31, 2018
PubMed

Insights

Malignant hypertension causes severe organ damage, particularly to the brain and heart. Treatment with renin-angiotensin system blockers shows promising results in preserving kidney function.

Area of Science:

  • Nephrology
  • Cardiology
  • Neurology

Background:

  • Malignant hypertension is a severe form of hypertension characterized by high blood pressure and acute ischemic organ damage.
  • It has a worse prognosis than other hypertensive forms, particularly in Black patients.
  • Advanced diagnostic tools for heart and brain organ damage can improve patient evaluation.

Purpose of the Study:

  • To enhance understanding of organ damage characteristics in malignant hypertension.
  • To facilitate diagnosis and evaluate treatment effectiveness for malignant hypertension.

Main Methods:

  • A registry of 168 malignant hypertension patients was analyzed.
  • Systematic cardiac (ECG, echocardiography) and brain (MRI) evaluations were performed.
  • Treatment involved a protocol of renin-angiotensin system blockers with forced oral titration.

Main Results:

  • Significant brain damage was detected in 93% of patients via MRI.
  • High prevalence of heart involvement (82% left ventricular mass, 56% systolic dysfunction).
  • Renal involvement (55%) and thrombotic microangiopathy (15%) were noted; 5-year renal survival was 90.8%.

Conclusions:

  • Malignant hypertension is a systemic disease affecting brain, heart, kidneys, and eyes, often asymptomatically.
  • Renin-angiotensin system blockers are crucial for managing malignant hypertension and preserving renal function.
Abstract

Related Concept Videos

Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors01:28

Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors

Phosphodiesterase 5 (PDE5) inhibitors are potent enzymes that function to hydrolyze cyclic nucleotides to their corresponding 5' monophosphates. Their unique biochemical properties have been applied in treating Pulmonary Arterial Hypertension (PAH).
Among the PDE5 inhibitors, sildenafil (Revatio) stands out as a competitive and selective inhibitor. It operates by elevating cellular levels of cGMP and augmenting signaling through the cGMP-PKG pathway, promoting vasodilation. Upon oral...
613
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists01:18

Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists

Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
471
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists01:23

Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists

Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
509
Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure01:16

Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure

Oxygen therapy has emerged as a significant tool in enhancing the quality of life for patients suffering from pulmonary arterial hypertension (PAH). While this therapy has principally been studied on patients with significant hypoxemia, this therapeutic approach helps prevent potential organ damage and can be administered in the comfort of one's home.
Oxygen therapy is vital in increasing and maintaining blood oxygen levels in PAH patients. As a result, it aids in reducing fatigue,...
625
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers01:26

Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
544
Hypertension I: Introduction01:28

Hypertension I: Introduction

Hypertension is a widespread, long-term medical condition where blood pressure in the arteries remains elevated. It is characterized by systolic blood pressure readings of 130 mm Hg or above or diastolic blood pressure (DBP) readings of 80 mm Hg or higher. Unmanaged hypertension poses significant health risks, making the distinction between primary (or essential) hypertension and secondary hypertension crucial, as their management and implications vary.Primary HypertensionPrimary hypertension,...
902