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The Left Pneumonectomy Combined with Monocrotaline or Sugen as a Model of Pulmonary Hypertension in Rats
Published on: March 8, 2019
Pulmonary hypertension complicating multiple myeloma
Udhay Krishnan1, Tomer M Mark2, Ruben Niesvizky2
1Division of Cardiology, Weil Cornell Medical College, New York Presbyterian Hospital-Cornell Medical Center, New York, New York, USA.
Abstract:
Pulmonary hypertension (PH) is an infrequently reported complication of multiple myeloma (MM). PH has been more commonly associated with amyloidosis, myeloproliferative diseases, and the POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes) syndrome. PH in MM is typically mild to moderate and may be secondary to a variety of conditions, which include left ventricular dysfunction, high-output cardiac failure, chronic kidney disease, treatment-related toxicities, and precapillary involvement. We describe 3 patients with MM and severe PH. Each patient underwent right heart catheterization. All patients demonstrated elevated pulmonary pressures, transpulmonary gradients, and pulmonary vascular resistance. Each patient was ultimately treated with pulmonary vasodilator therapy with improvement in cardiopulmonary symptoms. Additional studies are needed to define the prevalence, prognosis, and pathogenesis of PH in this complex population and to help clarify who may benefit from targeted PH therapy.
Insights
Pulmonary hypertension (PH) is a rare complication of multiple myeloma (MM). This study found severe PH in three MM patients, who improved with vasodilator therapy, suggesting a potential treatment target.
Area of Science:
- Hematology
- Cardiology
- Pulmonology
Background:
- Pulmonary hypertension (PH) is an uncommon complication of multiple myeloma (MM).
- PH is more frequently linked to conditions like amyloidosis, myeloproliferative diseases, and POEMS syndrome.
- In MM, PH is often mild to moderate and multifactorial, including cardiac dysfunction, kidney disease, and treatment side effects.
Observation:
- This report details three patients with multiple myeloma (MM) who presented with severe pulmonary hypertension (PH).
- All patients underwent right heart catheterization, confirming elevated pulmonary pressures, transpulmonary gradients, and pulmonary vascular resistance.
- The observed cases highlight a severe manifestation of PH in the context of MM.
Findings:
- The three patients with severe PH associated with MM were treated with pulmonary vasodilator therapy.
- Cardiopulmonary symptoms showed improvement following the initiation of vasodilator treatment.
- These findings suggest that pulmonary vasodilator therapy may be beneficial for select MM patients with severe PH.
Implications:
- Further research is essential to determine the prevalence and prognosis of PH in multiple myeloma patients.
- Understanding the pathogenesis of PH in MM is crucial for identifying patients who could benefit from targeted PH therapies.
- This study underscores the need for increased awareness and investigation of severe PH as a complication of multiple myeloma.
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