• Home
  • About Us
  • Blog

Pulmonary Hypertension RN

  • What is Pulmonary Hypertension?
    • What is Pulmonary Hypertension?
    • Pulmonary Hypertension Symptoms
    • Types of Pulmonary Hypertension
    • Causes of Pulmonary Hypertension
    • PH vs. PAH
    • Diastolic Heart Failure vs. PAH
    • WHO Group 3 Pulmonary Hypertension, IPF & COPD
    • Pulmonary Veno-Occlusive Disease
    • Hereditary Hemorrhagic Telangiectasia (HHT)
      • Hereditary Hemorrhagic Telangiectasia (HHT) Treatment
    • Functional Classification of Pulmonary Hypertension
    • Congenital Heart Disease
      • Eisenmenger’s Syndrome
      • Update on Management of PAH-CHD
      • Congenital Heart Disease & Sleep Apnea
      • Complex Congenital Heart Disease
      • Atrial Septal Defect and Pulmonary Arterial Hypertension
    • Pediatric Pulmonary Arterial Hypertension
    • Sickle Cell and Pulmonary Hypertension
    • Stimulant Associated Pulmonary Arterial Hypertension
    • Porto-Pulmonary Syndrome
    • Research, Life Expectancy & Prognosis for PH
  • Diagnosing & Monitoring PAH
    • Pulmonary Arterial Hypertension Diagnosis
    • How Am I Doing? Assessing Your PAH.
    • Blood Tests
    • Cardiopulmonary Exercise Test (CPET)
    • CT (Computed Tomography) Scan
    • Echocardiogram: An Overview
    • Echocardiogram: A Detailed Look
    • Pulmonary Function Tests (PFTs)
    • Right Heart Catheterization
    • Six Minute Walk
    • Ventilation Perfusion Scan (VQ Scan)
    • CTEPH
      • CTEPH: WHO Group 4 Pulmonary Hypertension
      • PTE (Pulmonary Thromboendarterectomy) Surgery
      • Adempas used to Treat PAH and CTEPH
  • PAH Treatment
    • Pulmonary Hypertension Centers
    • Pulmonary Hypertension Treatments
    • Continuously Infused Therapies Used to Treat PH
    • Prostanoids for Treatment of PH
    • Adcirca and Revatio Used to Treat Pulmonary Arterial Hypertension (PAH)
    • Adempas used to Treat PAH and CTEPH
    • Tracleer, Letairis, and Opsumit Treatments
    • Oxygen Therapy for Pulmonary Hypertension
    • Salt and Water Restrictions
    • Exercise & PAH
    • Diuretics
    • Blood Thinners
    • Getting the Most Out of PAH Therapy
      • Letairis
      • Opsumit
      • Sildenafil (Revatio)
  • Research
  • FAQ’s
    • Implanted Remodulin Pump, Right Heart Catheterization, PAH & Pregnancy
    • Oral Treatments, Care Centers & Hole in Heart
    • FAQ’s: Altitude, Cold & Allergy Medications
    • FAQ’s: Psoriasis, Idiopathic PAH, Contraceptives & PAH
    • FAQ’s: Causes of Pulmonary Hypertension, Symptom Frequency & Care Centers
    • FAQ: PAH Experts, Pregnancy, Mild PAH & Vacationing
    • FAQ’s: CTEPH, Blood Clots, Corrective Surgery & PAH Care Centers
    • FAQ’s: VQ Scans & PAH Curable?
    • FAQ’s: Mild Pulmonary Hypertension?
    • FAQ’s: Boating, Swimming & Eating with PAH
    • FAQ’s: Borderline Pulmonary Hypertension, Hand Swelling, Children with PAH, Costs

Zika Tips for Pulmonary Hypertension Patients

September 30, 2016 By Dr. Jeremy Feldman

mosquito zika virus What is Zika?

Zika is a virus spread via infected mosquitoes or from having sex with an infected individual. Most cases are being reported in South America but recently two neighborhoods in Miami, Florida have also been identified as having Zika carrying mosquitoes. Most people that are infected with Zika will not have much of an illness (perhaps some flu-like symptoms).  However, if a woman contracts the virus while pregnant it can cause serious birth defects—especially microcephaly (babies born with very small brains and heads). Another rare complication of Zika infection is a neurologic disorder called Guillain-Barré syndrome.  Patients experience progressive weakness in the arms and legs.  Currently there is no vaccine or medication to treat Zika.

Will Zika Make My Pulmonary Hypertension Worse?

The most common symptoms of Zika are fever, rash, joint pain, red eyes, muscle pain, and headache. These symptoms are mild and usually last for less than a week. Most patients, including PAH patients, will not become ill enough to go to the hospital and may not even realize they have the virus. The virus remains in the blood for about seven days and can be detected by blood work.

The Zika virus is most dangerous for pregnant women because it can cause birth defects.  Women with Pulmonary Arterial Hypertension are regularly counseled not to become pregnant. If a female Pulmonary Hypertension patient became pregnant and contracted the Zika virus she would have an increased risk of complications and birth defects.

How Can I Prevent Zika?

The best way to prevent getting Zika is to prevent mosquito bites.  Avoid known areas of Zika carrying mosquitoes. Wear long-sleeved shirts and pants when outside in areas where mosquitoes are present. Remove standing water from around your home.  Use air conditioning or ensure that window and door screens are intact.  Insect repellent is also a great defense.

Filed Under: Living with PAH

PAH Life Expectancy

PAH Research

Research, Life Expectancy & Prognosis for PH

Major Developments in Pulmonary Hypertension Affecting Prognosis 1.     Approval of

Where to Get Treatment?

CCCs for PAH

Pulmonary Hypertension Centers

Where to get treatment for pulmonary hypertension? Pulmonary arterial hypertension is a

Popular Posts

PAH patient with cold or flu virus

Flu Vaccine for PAH Patients

By Dr. Jeremy Feldman

It is hard to believe that summer is almost over and fall is about to begin.  As kids get ready to go back to school we

financial assistance for PAH patients

Copay Assistance from PAN Foundation Now Open

By Dr. Jeremy Feldman

The PAN Foundation announced that they have funds to help patients.  They have grants available for up to $5,300.  You

good news in pah

 

Disclaimer

Recent Blog Posts

  • In Memoriam:  Greg Ahearn, MD June 16, 2024
  • Sotatercept (Winrevair) Approved! June 1, 2024
  • Disappointing News for Rodatristat Ethyl October 11, 2023

Categories

Archives