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html/08/e5/08e5bd4a-766f-4c4e-869f-6a06ea9ab8d0_nodriver.html.gz

STS ACSD Operative Risk Calculator

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$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify1717897', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the planned surgery for this patient. Select MV Repair for Primary MR to go to the risk calculator specific to isolated mitral valve repair (MVr) surgery for primary mitral regurgitation(MR) and degenerative mitral etiology. For other isolated MVr, choose 'MV Repair - Any Etiology'.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('vstrpr', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient underwent tricuspid valve repair prcedure'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify924223', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate if this is first cv surgery for the patient or a reOp (first, second..) within the same anatomical space.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify6354278', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the clinical status of the patient prior to entering the operating room.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify7457762', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the patients sex at birth as either male or female.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify8726858', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the patients age in years (1-110 years) at time of surgery.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify8224332', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the height (20-251 cm) of the patient in centimeters closest to time of OR entry for index procedure.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify197100', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the weight (10-250 kg) of the patient in kilograms closest to time of OR entry for index procedure.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify5034235', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'System calculated BMI'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify7836407', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the patients race(s) and ethnicity (Hispanic, Latino or Spanish ethnicity) selecting all that apply.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify6257176', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the patients payor information (Maximum of 2 selections) from the following options: 1. None / self, 2. Medicare (any type) i.e. Medicare including commercially managed options, 3. Medicaid (any type) i.e. Medicaid including commercially managed options, 4.Commercial i.e. Commerical Health insurance, 5. HMO i.e. Health Maintenance Organization, 6. Military, 7. Non-U.S. Plan, 8. Other'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify1017069', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the creatinine level (0.1-30 mg/dL) closest to the date and time prior surgery but prior to anesthetic management (induction area or operating room). A creatinine level should be collected on all patients, even if they have no prior history of renal disease. A creatinine value is a high predictor of a patients outcome and is used in the predicted risk models.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify7119211', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the pre-operative Hematocrit level (1-99.99%) at the date and time closest to surgery but prior to anesthetic management (induction area or operating room). Capture only measured hematocrit levels, not calculated values.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify3068197', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the pre-operative White Blood Cell (WBC) (0.10-99.99 10³/μL) closest to the date and time prior to surgery but prior to anesthetic management (induction area or operating room).'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify8066697', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the platelet (1,000-900,000 cells/μL) closest to the date and time prior to surgery but prior to anesthetic management (induction area or operating room).'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('medacei48', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient received ACE Inhibitors or ARB within 48 hours prior to OR Entry.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('medgp', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient received Glycoprotein IIb/IIIa inhibitors within 24 hours preceding surgery.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('medinotr', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient received IV inotropic agents within 48 hours preceding surgery.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('medster', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient was taking steroids within 24 hours of surgery. This does not include a one-time dose related to prophylaxis therapy (i.e. IV dye exposure for cath procedure or surgery pre-induction period). Non-systemic medications are not included in this category (i.e., nasal sprays, topical creams).'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('medadp5days', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient has received ADP Inhibitors within 5 days preceding surgery.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('medadpidis', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate the number of days prior to surgery ADP Inhibitor use was discontinued. If less than 24 hours, enter 0.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify1736507', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether patient has a history of diabetes (Type I or II) diagnosed and/or treated by a healthcare provider. If yes, indicate the patient’s diabetes control method at home. Choose the most aggressive therapy.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('fhcad', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate if the patient has any direct blood relatives (parents, siblings, children) who have had any of the following at age <55 y for male relatives or <65 y for female relatives:  ? Angina  ? Acute MI  ? Sudden cardiac death without obvious cause  ? CABG surgery  ? PCI'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('hypertn', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate if the patient has a current diagnosis of hypertension defined by any 1 of the following: ? History of hypertension diagnosed and treated with medication, diet, and/or exercise  ? Currently undergoing pharmacological therapy for treatment of hypertension  2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J Am Coll Cardiol 2018;71:e127-e248.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('liverdis', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient has a history of hepatitis B, hepatitis C, drug induced hepatitis, auto-immune hepatitis, cirrhosis, portal hypertension, esophageal varices, liver transplant, or congestive hepatopathy. Exclude fatty liver, Hep A/E, NASH in the absence of cirrhosis. Refer to training manual for a full list of exclusions.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('mediastrad', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether patient has a history of radiation therapy to the mediastinum or chest.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('unrespstat', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient has a history of non-medically induced, unresponsive state within 24 hours of the time of surgery. Patient experienced complete mental unresponsiveness and no evidence of psychological or physiologically appropriate responses to stimulation, includes patients who experience sudden cardiac death.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('dialysis', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient is currently (prior to surgery) undergoing dialysis on a routine basis.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('cancer', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient has cancer or has a history of cancer diagnosed within 5 years of procedure. Do not capture low grade skin cancers such as basal cell or squamous cell carcinoma.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('syncope', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient had a sudden loss of consciousness with loss of postural tone, not related to anesthesia, with spontaneous recovery and believed to be related to cardiac condition. Capture events occurring within the past one year as reported by patient or observer. Patient may experience syncope when supine. Exclude vasovagal syncope.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('immsupp', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether immunocompromise is present due to immunosuppressive medication therapy within 30 days preceding the operative procedure or existing medical condition. The intent is to capture patients who are on chronic immunosuppressive medications for the treatment of a chronic underlying condition not a short-term treatment of an acute condition.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify1406195', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether the patient has a history of endocarditis documented and diagnosed by a Provider and the type of endocarditis. If the patient is currently being treated with antibiotic medication (other than prophylactic medication) for endocarditis (culture positive or negative), the disease is considered active. This includes patients with pre-operative endocarditis who will begin antibiotics post-op. If no antibiotic medication (other than prophylactic medication) is being given at the time of surgery AND the cultures are negative, then the infection is considered treated.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify9679107', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether there is documented history of use of illicit drugs, such as heroin, cocaine, or methamphetamine, or abuse of a controlled substance within the last year. Exclude cannabis.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify1927989', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Specify current alcohol use (within 30 days of surgery): ≤ 1 drink per week - rare or occasional drink; 2-7 drinks per week - Social; ≥ 8 drinks per week - Heavy drinker; None - Non-drinker'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify9241185', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate current (within 30 days prior to admission) or previous use of any tobacco product, including Cigarettes, Pipe, Cigars, Smokeless Cans, Other tobacco products (orbs, strips, sticks, hookah, etc.).'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify1343952', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether the patient has chronic lung disease, & the severity level based on following classification: No; Mild - FEV1 predicted = 60-75% or DLCO predicted = 61% to < your site’s lower limit for DLCO or on chronic inhaled or oral bronchodilator therapy; Moderate - FEV1 = 50-59% or DLCO = 40-60% or on chronic oral/systemic steroid therapy for lung disease; Severe - FEV1 <50% or DLCO <40% or Room Air pO2 < 60 or pCO2 > 50; CLD present, unknown severity; Unknown'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('pneumonia', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether patient has a recent (within 30 days) of pneumonia.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('slpapn', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether patient has a diagnosis of sleep apnea (may be described as obstructive sleep apnea or OSA).'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('hmo2', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether supplemental oxygen at home is prescribed and used.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify4059903', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the patient\'s worst current/history of CVD in the following order: a.Stroke (CVA) within 30 days of surgery b. CVA > 30 days i.e. remote c. CVA timing unk - Prior CVA but not known if <=30 or > 30 days ago d. TIA e. Any other CVD except a-d such as ≥ 50% stenosis of any major extra or intracranial vessels to the brain, vertebral artery disease and/or internal carotid disease and/or intracranial disease ≥ 50% stenosis(excluding external carotid disease), previous cervical or cerebral artery revascularization surgery or percutaneous intervention, Brain/cerebral aneurysm, occlusion of veterbral, internal carotid, and intracranial artery due to dissection (excluding chronic (nonvascular) neurological diseases or other acute neurological insults such as metabolic and anoxic ischemic encephalopathy). Subdural hematoma or AVM is not CVD.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('pvd', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient has a documented history of peripheral arterial disease (includes upper and lower extremity, renal, mesenteric, and abdominal aortic systems). This can include: 1. Claudication, either with exertion or at rest, 2. Amputation for arterial vascular insufficiency, 3. Vascular reconstruction, bypass surgery, or percutaneous intervention to the extremities (excluding dialysis fistulas and vein stripping), 4. Documented abdominal aortic aneurysm with or without repair. 5. Documented subclavian artery stenosis. 6. Documented chronic stable abdominal aortic dissection. 7. Documented peripheral artery aneurysms. PVD does not include disease in the carotid, cerebrovascular arteries or thoracic aorta, DVT, pulmonary artery aneurysm, Raynauds Disease or AVM.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('cvdstenrt', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate the severity of stenosis reported on the right carotid artery.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('cvdpcarsurg', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient has a history of previous carotid artery surgery and/or stenting.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('cvdstenlft', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate the severity of stenosis reported on the left carotid artery.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify2017392', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether heart failure is acute, chronic or both (acute on chronic)'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify5792503', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the patient\'s worst dyspnea or functional class, coded as the New York Heart Association (NYHA) classification documented by a MD/Provider within the past 2 weeks.<br/>There must be physician provider documentation in the medical record indicating the NYHA class. The NYHA Class is often used to document functional class and may or may not be associated with a diagnosis of heart failure.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify3244788', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the preoperative presence of Mechanical Cardiac Assist Devices of any kind'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify9555556', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the Ejection Fraction (1-99%) (percentage of the blood emptied from the left ventricle at the end of the contraction).'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('carshock', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate if the patient developed cardiogenic shock at the time of procedure.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('resusc', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether the patient required cardiopulmonary resuscitation within 1 hour of the start of the procedure.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify531578', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the patients worse symptom prior to surgery from Admission to OR Entry. For elective patients, choose the CAD presentation that is bringing them into the hospital.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify3611939', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether patient had a myocardial infarction and if so, indicate the time period between the last documented MI and surgery.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify2747395', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the number of diseased major native coronary vessel systems. A vessel that has ever been considered diseased, should always be considered diseased.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('stenleftmain', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate if left main stenosis greater or equal to 50%; number of diseased vessels must be greater than or equal to 1'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('laddiststenpercent', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate if the patients LAD distribution stenosis percentage is greater than or equal to 70%.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('vdstena', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether Aortic Stenosis is present.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('vdstenm', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether Mitral Stenosis is present.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('vdaoprimet', 'tooltip', {'container': 'body', 'placement': 'right', 'trigger': 'hover', 'title': 'Indicate whether aortic root abscess was the primary etiology of aortic valve disease.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify561163', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the degree of aortic valve insufficiency/regurgitation.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify9265418', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the degree of mitral valve insufficiency/regurgitation.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify6375798', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the degree of tricuspid valve insufficiency/regurgitation.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify1413442', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether arrhythmia was atrial fibrillation. Select remote if present > 30 days preoperatively and recent if present within 30 days of this procedure'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify5679256', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the type of atrial fibrillation.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify9845712', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether arrhythmia was atrial flutter. Select remote if present > 30 days preoperatively and recent if present within 30 days of this procedure'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify7981154', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether arrhythmia was VTach or VFib. Select remote if present > 30 days preoperatively and recent if present within 30 days of this procedure'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify5691558', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether arrhythmia was sick sinus syndrome. Select remote if present > 30 days preoperatively and recent if present within 30 days of this procedure'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify5613593', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether arrhythmia was second degree heart block. Select remote if present > 30 days preoperatively and recent if present within 30 days of this procedure'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify4985753', 'tooltip', {'container': 'body', 'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether arrhythmia was third degree heart block. Select remote if present > 30 days preoperatively and recent if present within 30 days of this procedure'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify5787055', 'tooltip', {'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether the patient has undergone any previous cardiovascular intervention, either surgical or non-surgical, which may include those done during the current admission.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify6227721', 'tooltip', {'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate the previous valve procedure/s.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify4334854', 'tooltip', {'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate whether previous Percutaneous Coronary Intervention (PCI) was performed within this episode of care at this facility and the interval of time between the most recent PCI and the planned surgical procedure. Episode of care is defined as continuous inpatient hospitalization which includes transfer from one acute care hospital to another.'})}, 500)});

$(document).ready(function() {setTimeout(function() {shinyBS.addTooltip('tipify2903594', 'tooltip', {'placement': 'bottom', 'trigger': 'hover', 'title': 'Indicate other cardiac interventions that were performed.'})}, 500)});

Requests	IP Address	Location	AS Autonomous System
15	162.159.140.98	United States	AS13335Cloudflare, Inc.
14	142.251.127.97	United States	AS15169Google LLC
29	2	-	-

Security Scan Report: acsdriskcalc.research.sts.org

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