Skip to main content

SYNERGY™ XD Monorail Coronary Stent System – Indications, Safety and Warnings

Return to product detail page

CAUTION: Federal law (USA) restricts this device to sale by or on the order of a physician. Rx only. Prior to use, please see the complete “Instructions for Use” for more information on Indications, Contraindications, Warnings, Precautions, Adverse Events, and Operator’s Instructions.

INDICATIONS FOR USE

The SYNERGY™ XD Everolimus-Eluting Platinum Chromium Coronary Stent System is indicated for improving luminal diameter in patients, including those with diabetes mellitus, with symptomatic heart disease, stable angina, unstable angina, non-ST elevation MI or documented silent ischemia due to atherosclerotic lesions in native coronary arteries ≥2.25 mm to ≤5.00 mmin diameter in lesions ≤44 mm in length and for high bleeding risk patients with coronary arteries ≥2.25 mm to ≤5.00 mm in diameter in lesions ≤34 mm in length.

CONTRAINDICATIONS
Use of the SYNERGY XD Everolimus-Eluting Platinum Chromium Coronary Stent System is contraindicated in patients with known hypersensitivity to:

  • 316L stainless steel, platinum, chromium, iron, nickel or molybdenum.
  • Everolimus or structurally-related compounds
  • The polymer or their individual components (see Section 2.4.2 Polymer Carrier in the eIFU) Coronary Artery Stenting is contraindicated for use in:
  • Patients judged to have a lesion that prevents complete inflation of an angioplasty balloon or proper placement of thestent or delivery device.
  • Patients with uncorrected bleeding disorders or patients who cannot receive anticoagulation or antiplatelet aggregation therapy (see Section 6.2 Pre- and Post-Procedure Antiplatelet Regimen for more information in the eIFU).

WARNINGS

  • To maintain sterility, the package should not be opened or damaged prior to use.
  • The use of this product carries the risks associated with coronary artery stenting, including stent thrombosis, vascular complications, and/or bleeding events.
  • This product should not be used in patients who are not likely to comply with recommended antiplatelet therapy.

GENERAL PRECAUTIONS

  • Prior to angioplasty, carefully examine all equipment to be used during the procedure including the dilatation catheter to verify proper function.
  • Careful consideration should be given to the risks and benefits of use in patients with history of severe reaction to contrast agents.
  • Stent thrombosis is a rare event and is frequently associated with myocardial infarction (MI) or death. In the clinical trials analyzed to date, differences in the incidence of stent thrombosis have not been associated with an increased risk of cardiac death, MI, or all-cause mortality.
  • When DES are used outside the specified indications for Use, patient outcomes may differ from the results observed during the EVOLVE clinical trials.
  • Compared to use within the specified Indications for Use, the use of DES in patients and lesions outside of the labeled indications may have an increased risk of adverse events, including stent thrombosis, stent embolization, MI or death. When treating such patients, physicians should be aware of this increased risk and consider available data and the limitations of such data.
  • Used devices may pose a biohazard risk and must be handled and disposed of properly.

Pre- and Post-Procedure Antiplatelet Regimen

The optimal duration of antiplatelet therapy, specifically P2Y12 inhibitor therapy is unknown and DES thrombosis may still occur despite continued therapy beyond current professional society guidelines.

Oral Antiplatelet Therapy

Continuation of combination treatment with aspirin and a P2Y12 inhibitor after PCI appears to reduce major adverse cardiac events. On the basis of randomized clinical trials the 2016 ACC/AHA guidelines recommend aspirin 81 mg daily should be given indefinitely after PCI. In patients who are not at high risk of bleeding, a P2Y12 inhibitor should be given daily for at least 6 months in stable ischemic heart disease patients and for at least 12 months in acute coronary syndrome (ACS) patients. Full guidelines are provided at the following website: http://www.onlinejacc.org Based upon the results of the EVOLVE Short DAPT Study the SYNERGY XD stent can be safely used in conjunction with shortened DAPT in patients at high risk for bleeding. In the EVOLVE Short DAPT Study, high bleeding risk subjects were defined as meeting one or more of the following criteria: ≥75 years of age and, in the opinion of the investigator, the risk of bleeding associated with >3 months of DAPT outweighs the benefit; need for chronic or lifelong anticoagulation, history of major bleeding (severe/life threatening or moderate bleeding based on the GUSTO classification) within 12 months of the index procedure; history of stroke (ischemic or hemorrhagic); renal insufficiency (creatinine ≥2.0 mg/dl) or failure (dialysis dependent); platelet count ≤100,000/μL. It is very important that the patient is compliant with the post-procedural antiplatelet recommendations. Premature discontinuation of prescribed antiplatelet medication could result in a higher risk of thrombosis, MIor death. Prior to PCI, if a surgical or dental procedure is anticipated that requires early discontinuation of antiplatelet therapy, the interventional cardiologist and patient should carefully consider whether a DES and its associated recommended antiplatelet therapy is the appropriate PCI choice.

Pediatric Use

The safety and effectiveness of the SYNERGY Stent in pediatric patients have not been established.

Lesion/Vessel Characteristics

The safety and effectiveness of the SYNERGY Stent have not been established in the cerebral, carotid, or peripheral vasculature or in the following patient populations:

  • Patients with vessel thrombus at the lesion site.
  • Patients with coronary artery reference vessel diameters <2.25 or >5.00 mm.
  • Patients with coronary artery lesions longer than 44mm or requiring more than one SYNERGY Stent.
  • Patients with lesions located in saphenous vein grafts, in the left main coronary artery, ostial location, or complexbifurcation (e.g. bifurcation lesion requiring treatment with more than one stent).
  • Patients with diffuse disease or reduced blood flow distal to the identified lesions.
  • Patients with a recent acute ST elevation myocardial infarction where there is evidence of thrombus or poor flow.
  • Patients with in-stent restenosis.
  • Patients with a chronic total occlusion.
  • Patients with 3 vessel disease.

Magnetic Resonance Imaging (MRI) Safety Information:

Non-clinical testing has demonstrated that the SYNERGY XD Stent is MR Conditional for single and overlapped conditions upto 94 mm. A patient with this device can be safely scanned in a Magnetic Resonance system meeting the following conditions. Failure to follow these conditions may result in injury to the patient. If information about a specific parameter is not included, there are no conditions associated with that parameter.

  • Static magnetic field of 3.0 and 1.5 Tesla only
  • Maximum spatial gradient magnetic field of 2300 gauss/cm (23 T/m)
  • Maximum Magnetic Resonance system reported, whole body averaged specific absorption rate (SAR) of ≤2 W/kg(Normal Operating Mode)
  • Scanner Type: Horizonal, Cylindrical bore
  • Maximum gradient slew rate per axis [T/m/s]: max. 80 mT/m/ms (1.5 T), 200 mT/m/ms (3.0 T)
  • RF Excitation: CP (Circular Polarization) 90
  • RF Transmit/ Receive Coil Type: Integrated Whole-Body Transmit/Receive Coil
  • Scan Duration: Up to 15 minutes of continuous RF (a sequence or back-to-back series/ scan without breaks), followed by 5 minutes of cooling. 

Under the scan conditions defined above, the SYNERGY XD Stent is expected to produce a maximum temperature rise of 5˚ Corless after 15 minutes of continuous scanning. MR Image quality may be compromised if the area of interest is within the lumen or relatively near the stent. Therefore, it maybe necessary to optimize MR imaging parameters for the presence of the stent. The image artifact extends approximately 1 cm from the stent when scanned in non-clinical MR testing specified in ASTM F2119-07. The artifact does obscure the device lumen. Image artifact was minimized using the spin echo sequence versus gradient echo.

POTENTIAL ADVERSE EVENTS

Potential adverse events (in alphabetical order) which may be associated with the use of a coronary stent in native coronaryarteries include but are not limited to:

  • Allergic or adverse reaction (including medications, anesthesia, contrast, or device material
  • Angina
  • Arrhythmias, including ventricular fibrillation, ventricular tachycardia and heart block
  • Bleeding including hemorrhage or hematoma (possibly requiring transfusion or additional intervention)
  • Cardiac failure leading to low cardiac output (cardiogenic shock) or pulmonary edema
  • Death
  • Emboli (including air, tissue, thrombus, or device materials)
  • Fever and pyrogen reaction
  • Heart failure
  • Hypotension/hypertension
  • Infection, local or systemic
  • Myocardial infarction
  • Pain, or inflammation
  • Pericarditis, pericardial effusion or tamponade
  • Radiation injury
  • Renal insufficiency or failure
  • Respiratory insufficiency or failure
  • Restenosis or late acquired malapposition of treated segment
  • Stent placement issues including geographic miss, malapposition, migration, or embolization
  • Stent thrombosis/vessel occlusion
  • Stroke/cerebrovascular accident/transient ischemic attack
  • Vessel injury (including access-site) such as spasm, lymphatic problems, pseudoaneurysm, arteriovenous fistula,trauma, dissection, occlusion, perforation and, rupture 

 

Zortress, the oral formulation of everolimus developed by Novartis Pharmaceuticals Corporation, has been evaluated in clinical trials and is approved in the United States for the prevention of organ rejection in adult kidney transplant recipients at the dose of 1.5 mg/day. Outside the U.S., Zortress is sold under the brand name, Certican™, in more than 70 countries. Everolimus is also approved in the United States under the name of Afinitor™ for patients with advanced renal cell carcinoma (cancer), after failure of treatment with sunitinib or sorafenib, at doses of 5 to 20 mg/day when taken by mouth. The following list includes the known risks of everolimus at the oral doses listed above. The amount of drug that circulates in the bloodstream following implantation of a SYNERGY™ Stent is several folds lower than that obtained with oral doses (1.5 mg to 20 mg/day, see Section 7.2, Pharmacokinetics of the eIFU)). Adverse events associated with daily oral administration of everolimus (or potential adverse events not captured above, that may be unique to the everolimus drug coating) can be found in the labeling for finished pharmaceuticals containing everolimus, such as Afinitor or Zortress.

Top