{"id":650,"date":"2022-01-13T15:56:32","date_gmt":"2022-01-13T12:56:32","guid":{"rendered":"https:\/\/aventinhealth.com\/urunler\/uncategorized\/ellipse-icds-implantable-cardioverter-defibrillators\/"},"modified":"2022-01-13T15:56:32","modified_gmt":"2022-01-13T12:56:32","slug":"ellipse-icds-implantable-cardioverter-defibrillators","status":"publish","type":"product","link":"https:\/\/aventinhealth.com\/en\/urunler\/abbott-products\/cardiovascular-products\/implantable-cardioverter-defibrillators-icd\/ellipse-icds-implantable-cardioverter-defibrillators\/","title":{"rendered":"Ellipse\u2122 ICDs | Implantable Cardioverter Defibrillators"},"content":{"rendered":"
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Rx only<\/p>\n

Brief Summary:<\/strong>Before using these devices, please review the User Manual for a complete list of indications, contraindications, warnings, precautions, potential adverse events, and instructions for use.<\/p>\n

Indications:<\/strong> The devices are intended to provide ventricular antitachycardia pacing and ventricular defibrillation for the automated treatment of life-threatening ventricular arrhythmias. AF Suppression\u2122 pacing is indicated for the suppression of paroxysmal or persistent atrial fibrillation in patients with the above ICD indication and sinus node dysfunction.<\/p>\n

Contraindications: Contraindications to the use of the pulse generator system include ventricular tachyarrhythmias caused by transient or correctable factors such as drug toxicity, electrolyte imbalance, or acute myocardial infarction.<\/strong><\/p>\n

Adverse Events:<\/strong> Possible system-related adverse events (in alphabetical order) include, but are not limited to:<\/p>\n

    \n
  • Acceleration of arrhythmias (device-induced)<\/li>\n
  • Air embolism<\/li>\n
  • Allergic reaction<\/li>\n
  • Bleeding<\/li>\n
  • Cardiac tamponade<\/li>\n
  • Chronic nerve damage<\/li>\n
  • Death<\/li>\n
  • Erosion<\/li>\n
  • Exacerbation of heart failure<\/li>\n
  • Excessive fibrotic tissue growth<\/li>\n
  • Extracardiac stimulation (phrenic nerve, diaphragm, chest wall)<\/li>\n
  • Extrusion<\/li>\n
  • Fluid accumulation<\/li>\n
  • Hematoma or cyst formation<\/li>\n
  • Inappropriate shocks<\/li>\n
  • Infection<\/li>\n
  • Keloid formation<\/li>\n
  • Lead wear and discontinuity<\/li>\n
  • Lead migration\/relocation<\/li>\n
  • Myocardial damage<\/li>\n
  • Pneumothorax<\/li>\n
  • Current or insulating myocardium during defibrillation with internal or external paddles<\/li>\n
  • Potential mortality due to defibrillation or inability to pace<\/li>\n
  • Thromboembolism<\/li>\n
  • Venous congestion<\/li>\n
  • Venous or cardiac perforation.<\/li>\n<\/ul>\n

    Patients susceptible to frequent shocks despite antiarrhythmic medical management may develop psychological intolerance to an ICD or CRT-D system that may include the following:<\/p>\n

      \n
    • Dependence<\/li>\n
    • Depression<\/li>\n
    • Fear of premature battery drain<\/li>\n
    • Fear of shock when conscious<\/li>\n
    • Fear of losing shock ability<\/li>\n
    • Phantom shocker (ghost shock)<\/li>\n<\/ul>\n

      See the User’s Guide for detailed indications, contraindications, warnings, precautions and potential adverse events.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

      Ellipse\u2122 ICD
      \nSingle Room<\/h3>\n

      CD1411-36Q<\/h4>\n

      Rx only<\/p>\n

      Brief Summary:<\/strong> Before using these devices, please review the User Manual for a complete list of indications, contraindications, warnings, precautions, potential adverse events, and instructions for use.<\/p>\n

      Indications:<\/strong> The devices are intended to provide ventricular antitachycardia pacing and ventricular defibrillation for the automated treatment of life-threatening ventricular arrhythmias. AF Suppression\u2122 pacing is indicated for the suppression of paroxysmal or persistent atrial fibrillation in patients with the above ICD indication and sinus node dysfunction.<\/p>\n

      Contraindications:<\/strong> Contraindications to the use of the pulse generator system include ventricular tachyarrhythmias caused by transient or correctable factors such as drug toxicity, electrolyte imbalance, or acute myocardial infarction.<\/p>\n

      Adverse Events:<\/strong> Possible system-related adverse events (in alphabetical order) include, but are not limited to:<\/p>\n

        \n
      • Acceleration of arrhythmias (device-induced)<\/li>\n
      • Air embolism<\/li>\n
      • Allergic reaction<\/li>\n
      • Bleeding<\/li>\n
      • Cardiac tamponade<\/li>\n
      • Chronic nerve damage<\/li>\n
      • Death<\/li>\n
      • Erosion<\/li>\n
      • Exacerbation of heart failure<\/li>\n
      • Excessive fibrotic tissue growth<\/li>\n
      • Extracardiac stimulation (phrenic nerve, diaphragm, chest wall)<\/li>\n
      • Extrusion<\/li>\n
      • Fluid accumulation<\/li>\n
      • Hematoma or cyst formation<\/li>\n
      • Inappropriate shocks<\/li>\n
      • Infection<\/li>\n
      • Keloid formation<\/li>\n
      • Lead wear and discontinuity<\/li>\n
      • Lead migration\/relocation<\/li>\n
      • Myocardial damage<\/li>\n
      • Pneumothorax<\/li>\n
      • Current or insulating myocardium during defibrillation with internal or external paddles<\/li>\n
      • Potential mortality due to defibrillation or inability to pace<\/li>\n
      • Thromboembolism<\/li>\n
      • Venous congestion<\/li>\n
      • Venous or cardiac perforation.<\/li>\n<\/ul>\n

        Patients exposed to frequent shocks despite antiarrhythmic medical therapy may develop psychological intolerance to an ICD or CRT-D system, which may include:<\/p>\n

          \n
        • Dependence<\/li>\n
        • Depression<\/li>\n
        • Fear of premature battery drain<\/li>\n
        • Fear of shock when conscious<\/li>\n
        • Fear of losing shock ability<\/li>\n
        • Phantom shocker (ghost shock)<\/li>\n<\/ul>\n

          See the User’s Guide for detailed indications, contraindications, warnings, precautions and potential adverse events.<\/p>\n","protected":false},"excerpt":{"rendered":"

          Designed for patient safety and comfort, the Ellipse\u2122 ICD offers a small doctor-designed shape, up to 36 J of delivered energy, highly adaptable, non-invasive programming options, and wireless remote monitoring with a Merlin@home\u2122 transmitter.<\/p>\n","protected":false},"featured_media":457,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_joinchat":[]},"product_brand":[],"product_cat":[545,546,548],"product_tag":[562],"class_list":{"0":"post-650","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-abbott-products","7":"product_cat-cardiovascular-products","8":"product_cat-implantable-cardioverter-defibrillators-icd","9":"product_tag-cardiac-rhythm-management","11":"first","12":"instock","13":"shipping-taxable","14":"product-type-simple","15":"prodpage-classic"},"yoast_head":"\nEllipse\u2122 ICDs | Implantable Cardioverter Defibrillators - Aventin Health<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/aventinhealth.com\/urunler\/uncategorized\/ellipse-icds-implantable-cardioverter-defibrillators\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Ellipse\u2122 ICDs | Implantable Cardioverter Defibrillators - 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