Cardiac catheterization pre-procedure evaluation resident survival guide: Difference between revisions

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{{familytree | | | | | C02 | | | | | | | | | | | | | | | | | | | | | |C02=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Confirm that the patient has ANY of the following indications for cardiac catheterization'''<br><br>
{{familytree | | | | | C02 | | | | | | | | | | | | | | | | | | | | | |C02=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Confirm that the patient has ANY of the following indications for cardiac catheterization'''<br><br>
'''''Left heart catheterization'''''<br>
'''''Left heart catheterization'''''<br>
❑ Canadian cardiovascular society (CCS) class III (i.e. symptoms with everyday living activities) or class IV angina (i.e. inability to perform any activity without angina or angina at rest) despite medical therapy, '''OR'''<br>
❑ Canadian cardiovascular society (CCS) class III (i.e. symptoms with everyday living activities) or class IV [[angina]] (i.e. inability to perform any activity without angina or angina at rest) despite medical therapy, '''OR'''<br>
❑ Angina plus systolic dysfunction, '''OR'''<br>
❑ Angina plus [[systolic dysfunction]], '''OR'''<br>
❑ Uncertain diagnosis following non-invasive test and need to confirm diagnosis, '''OR'''<br>
❑ Uncertain diagnosis following [[non-invasive test]] and need to confirm diagnosis, '''OR'''<br>
❑ Systolic dysfunction with unexplained cause, '''OR'''<br>
[[Systolic dysfunction]] with unexplained cause, '''OR'''<br>
❑ Survivor of sudden cardiac death, polymorphic VT, or sustained monomorphic VT, '''OR'''<br>
❑ Survivor of [[sudden cardiac death]], [[polymorphic VT]], or [[sustained monomorphic VT]], '''OR'''<br>
❑ Suspected spasm or non-atherosclerotic cause of ischemia, '''OR'''<br>
❑ Suspected [[coronary spasm|spasm]] or non-atherosclerotic cause of ischemia, '''OR'''<br>
❑ High-risk stress test finding, defined as '''ANY''' of following <ref name="pmid22326193">{{cite journal| author=Marso SP, Teirstein PS, Kereiakes DJ, Moses J, Lasala J, Grantham JA| title=Percutaneous coronary intervention use in the United States: defining measures of appropriateness. | journal=JACC Cardiovasc Interv | year= 2012 | volume= 5 | issue= 2 | pages= 229-35 | pmid=22326193 | doi=10.1016/j.jcin.2011.12.004 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22326193  }} </ref>:<br>
❑ High-risk [[stress test]] finding, defined as '''ANY''' of following <ref name="pmid22326193">{{cite journal| author=Marso SP, Teirstein PS, Kereiakes DJ, Moses J, Lasala J, Grantham JA| title=Percutaneous coronary intervention use in the United States: defining measures of appropriateness. | journal=JACC Cardiovasc Interv | year= 2012 | volume= 5 | issue= 2 | pages= 229-35 | pmid=22326193 | doi=10.1016/j.jcin.2011.12.004 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22326193  }} </ref>:<br>
:❑ Resting LVEF < 35%
:❑ Resting [[LVEF]] < 35%
:❑ High-risk treadmill score (≤ 11)
:❑ High-risk [[treadmill score]] (≤ 11)
:❑ Severe exercise LVEF < 35%
:❑ Severe [[exercise LVEF]] < 35%
:❑ Stress-induced large perfusion defect
:❑ Stress-induced large [[perfusion defect]]
:❑ Stress-induced multiple perfusion defects
:❑ Stress-induced multiple [[perfusion defect]]s
:❑ Large, fixed perfusion defect with LV dilation OR increased lung uptake
:❑ Large, fixed perfusion defect with [[LV dilation]] OR increased [[lung uptake]]
:❑ LV dilation or increased lung uptake
:❑ [[LV dilation]] or increased [[lung uptake]]
:❑ Stress-induced moderate perfusion defect with LV dilation or increased lung uptake<br><br>
:❑ Stress-induced moderate perfusion defect with [[LV dilation]] or increased [[lung uptake]]<br><br>


'''''Right heart catheterization'''''<br>
'''''Right heart catheterization'''''<br>
❑ Patient in shock with unknown volume status<br>
❑ Patient in [[shock]] with unknown volume status<br>
❑ Cardiogenic shock<br>
[[Cardiogenic shock]]<br>


❑ Diagnosis of follow-up of pulmonary artery hypertension<br>
❑ Diagnosis of follow-up of [[pulmonary artery hypertension]]<br>


❑ Patients with advanced cardiopulmonary diseases who require surgery<br>
❑ Patients with advanced [[cardiopulmonary diseases]] who require surgery<br>


:❑ Left-to-right shunt<br>
:❑ [[Left-to-right shunt]]<br>


:❑ Valvular disease<br>
:❑ [[Valvular disease]]<br>


:❑ Pulmonary artery hypertension<br>
:❑ [[Pulmonary artery hypertension]]<br>


:❑ Congenital heart disease</div>
:❑ [[Congenital heart disease]]</div>
}}
}}
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'''''History of Present Illness'''''<br>
'''''History of Present Illness'''''<br>


❑ Age<br>
[[Age]]<br>


❑ Chest pain or chest discomfort<br>
[[Chest pain]] or [[chest discomfort]]<br>


❑ Onset of symptoms<br>
❑ Onset of symptoms<br>


❑ Sensation of heaviness, tightness, pressure, or squeezing<br>
❑ Sensation of [[heaviness]], [[tightness]], [[pressure]], or [[squeezing]]<br>


❑ Duration of each episode<br>
❑ Duration of each episode<br>


❑ Radiation to the left arm, jaw, neck, right arm, back or epigastrium<br>
❑ Radiation to the [[left arm]], [[jaw]], [[neck]], [[right arm]], [[back]], or [[epigastrium]]<br>


❑ Timing of symptoms (morning vs. evening vs. wake patient at night)<br>
❑ Timing of symptoms (morning vs. evening vs. wake patient at night)<br>


❑ Alleviating factors (e.g. medications or rest)<br>
[[Alleviating factor]]s (e.g. [[medication]]s or [[rest]])<br>


❑ Exacerbating factors<br>
[[Exacerbating factor]]s<br>


❑ Association of symptoms to food intake<br>
❑ Association of symptoms with food intake<br>


❑ Palpitations<br>
[[Palpitations]]<br>


❑ Nausea or vomiting<br>
[[Nausea]] or [[vomiting]]<br>


❑ Sweating<br>
[[Sweating]]<br>


❑ Dyspnea<br>
[[Dyspnea]]<br>


❑ Orthopnea<br>
[[Orthopnea]]<br>


❑ Dizziness<br>
[[Dizziness]]<br>


❑ Weakness of extremities<br>
[[Weakness]] of extremities<br>


❑ Numbness of tingling of extremities<br>
[[Numbness]] or [[tingling]] of extremities<br>


❑ Lightheadedness<br>
[[Lightheadedness]]<br>


❑ Syncope or presyncope<br>
[[Syncope]] or [[presyncope]]<br>


❑ Increased frequency of symptoms<br>
❑ Increased frequency of symptoms<br>


❑ Worsening of symptom severity<br>
❑ Worsening of [[severity]]<br>


❑ Previous episodes<br>
❑ Previous episodes<br>


❑ Recent infections<br>
❑ Recent [[infection]]s<br>


❑ Fever<br>
[[Fever]]<br>


❑ Weight or appetite changes<br>
[[Weight change|Weight]] or [[appetite change]]s<br>


❑ Stress<br>
[[Stress]]<br>


❑ Fatigue<br><br>
[[Fatigue]]<br><br>


'''''Possible Symptom Triggers'''''<br>
'''''Possible Symptom Triggers'''''<br>


❑ Physical exertion<br>
[[Physical exertion]]<br>


❑ Air pollution or fine particulate matter<br>
[[Air pollution]] or fine particulate matter<br>


❑ Recent infection<br>
❑ Recent [[infection]]<br>


❑ Heavy meal intake<br>
[[Heavy meal intake]]<br>


❑ Cocaine<br>
[[Cocaine]]<br>


❑ Marijuana<br><br>
[[Marijuana]]<br><br>


'''''Cardiovascular Risk Factors'''''<br>
'''''Cardiovascular Risk Factors'''''<br>


❑ Known CAD (review available catheterizations or CABG reports)<br>
❑ Known [[CAD]] (review available [[cardiac catheterization]]s or [[CABG]] reports)<br>


❑ Smoking history<br>
[[Smoking]] history<br>


❑ Baseline blood pressure (Duration, antihypertensive therapy, compliance with medications)<br>
❑ Baseline [[blood pressure]] (Duration, [[antihypertensive therapy]], compliance with medications)<br>


❑ History of diabetes mellitus (Duration, DM control, compliance, antidiabetic medications, recent HbA1c, screening for micro- and macrovascular DM complications)<br>
❑ History of [[diabetes mellitus]] (Duration, DM control, compliance, [[antidiabetic medication]]s, recent [[HbA1C]], screening for [[Microvascular complications of diabetes|microvascular]] and [[Macrovascular complications of diabetes|macrovascular]] DM [[Complications of diabetes|complications]])<br>


❑ Dyslipidemia<br>
[[Dyslipidemia]]<br>


❑ Obesity (BMI > 30 kg/m2)<br><br>
[[Obesity]] ([[BMI]]> 30 kg/m2)<br><br>


'''''Past Medical History'''''<br>
'''''Past Medical History'''''<br>


❑ Congenital heart disease<br>
[[Congenital heart disease]]<br>


❑ Left to right shunts<br>
[[Left to right shunt]]s<br>


❑ Dextrocardia<br>
[[Dextrocardia]]<br>


❑ Situs inversus<br>
[[Situs inversus]]<br>


❑ History of renal disease (CrCl < 60 mL/min)? Does the patient currently have a stable renal function?<br>
❑ History of [[renal disease]] ([[CrCl]] < 60 mL/min)? Does the patient currently have a [[stable renal function]]?<br>


❑ History of bleeding tendency<br>
❑ History of [[bleeding tendency]]<br>


❑ Known significant anemia (Hct < 30%)<br>
❑ Known significant [[anemia]] (Hct < 30%)<br>


❑ History of heparin-induced thrombocytopenia (HIT)<br>
❑ History of [[heparin-induced thrombocytopenia]] (HIT)<br>


❑ History of pulmonary disease<br>
❑ History of [[pulmonary disease]]<br>


❑ History of major surgery in the past month<br>
❑ History of [[major surgery]] in the past month<br>


❑ Anticipated major surgery in the next year<br><br>
❑ Anticipated [[major surgery]] in the next year<br><br>


'''''Medications'''''<br>
'''''Medications'''''<br>
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❑ Prescribed drug<br>
❑ Prescribed drug<br>


❑ Home oxygen therapy<br>
❑ Home [[oxygen therapy]]<br>


❑ Over-the-counter drugs<br>
[[Over-the-counter drug]]s<br>


Herbs and supplements<br>
[[Herb]]s and [[supplement]]s<br>


❑ Administration of ANY of the following medications within the last 48 hours prior to catheterization?<br>
❑ Administration of ANY of the following medications within the last 48 hours prior to catheterization?<br>


:❑ Aspirin
:❑ [[Aspirin]]


:❑ Clopidogrel
:❑ [[Clopidogrel]]


:❑ Metformin
:❑ [[Prasugrel]]
:❑[[Ticagrelor]]


:❑ Phosphodiesterase inhibitors (e.g. Tadalafil, sildenafil, or similar drugs)
:❑ [[Metformin]]
:❑ Other [[oral antidiabetic agent]]s
:❑ [[Insulin injection]]s
:❑ [[Phosphodiesterase inhibitor]]s (e.g. [[Tadalafil]], [[sildenafil]], or [[vardenafil]])


:❑ Warfarin. If yes, what is most recent INR?
:❑ [[Warfarin]]. If yes, what is most recent INR?


:❑ Low molecular weight heparin (LMWH). If yes, when was last dose?
:❑ [[Unfractionated heparin]] or [[Low molecular weight heparin]] (LMWH). If yes, when was last dose?


:❑ Other chronic anticoagualants (e.g. dabigatran, NOACs, fondaparinux)<br><br>
:❑ Other chronic [[anticoagualant]]s (e.g. [[dabigatran]], [[NOAC]]s)<br><br>


'''''Allergies'''''<br>
'''''Allergies'''''<br>


❑ List of allergies, including severity and manifestations (pruritus, rash, hives, stridor, or anaphylactic shock)<br>
❑ List of allergies, including severity and manifestations ([[pruritus]], [[rash]], [[hives]], [[stridor]], or [[anaphylactic shock]])<br>


❑ Known drug allergies
❑ Known [[Drug allergy|drug allergies]]


:❑ Allergy to aspirin or history of nasal polyps or aspirin desensitization
:❑ Allergy to [[aspirin]] or history of [[nasal polyp]]s or [[aspirin desensitization]]


:❑ Allergy to heparin
:❑ Allergy to [[heparin]]
:❑ Allergy to sedation medications
:❑ Allergy to [sedative]]s
:❑ Other drug allergies
:❑ Other [[Drug allergy|drug allergies]]


:❑ Contrast allergy
:❑ [[Contrast allergy]]
:❑ Latex allergy
:❑ [[Latex allergy]]


:❑ Allergy to Shellfish (controversial association between shellfish allergy and contrast allergy)
:❑ [[Shellfish allergy|Allergy to shellfish]] (controversial association between shellfish allergy and contrast allergy)


:❑ Other known environmental and food allergies<br><br>
:❑ Other known environmental and food allergies<br><br>
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'''''Family History'''''<br>
'''''Family History'''''<br>


❑ Family history of premature cardiovascular diseases<br><br>
❑ Family history of premature [[cardiovascular disease]]s<br><br>


'''''Social and Sexual History'''''<br>
'''''Social and Sexual History'''''<br>


❑ Healthcare proxy and available family members for patient care<br>
[[Healthcare proxy]] and available family members for patient care<br>


❑ Barrier to tolerate or adhere to dual antiplatelet therapy (DAPT) or follow-up visits<br>
❑ Barrier to tolerate or adhere to [[dual antiplatelet therapy]] (DAPT) or follow-up visits<br>


❑ Pregnancy or possible pregnancy<br><br>
[[Pregnancy]] or possible pregnancy<br><br>


'''''Advanced Directives'''''<br>
'''''Advanced Directives'''''<br>


❑ DNR status<br>
[[Do not resuscitate|DNR]] status<br>


❑ DNI status</div>}}
[[Do not intubate|DNI]] status</div>}}
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{{familytree | | | | | E01 | | | | | | | | | | | | | | | | | | | | | |E01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Examine the patient'''<br><br>
{{familytree | | | | | E01 | | | | | | | | | | | | | | | | | | | | | |E01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Examine the patient'''<br><br>


❑ Vital signs, including BP, HR, RR, T, room air SpO2<br>
[[Vital signs]], including [[Blood pressure|BP]], [[Heart rate|HR]], [[Respiratory rate|RR]], [[Temperature|T]], room air [[Oxygen saturation|SpO2]]<br>


❑ Height (in meters), weight (in kilograms), and body mass index (BMI)<br>
[[Height]] (in meters), [[weight]] (in kilograms), and [[body mass index]] (BMI)<br>


❑ Level of consciousness, orientation, and ability to cooperate and communicate<br><br>
❑ Level of [[consciousness]], [[orientation]], and ability to cooperate and communicate<br><br>


'''''Skin'''''<br>
'''''Skin'''''<br>


❑ Xanthelesma or xanthoma (suggestive of dyslipidemia)<br>
[[Xanthelesma]] or [[xanthoma]] (suggestive of [[dyslipidemia]])<br>


❑ Edema (suggestive of congestive heart failure)<br>
[[Edema]] (suggestive of renal insufficiency or [[congestive heart failure]])<br>


❑ Acral and/or central cyanosis<br><br>
[[Acral cyanosis|Acral]] and/or [[central cyanosis]]<br><br>


'''''HEENT'''''<br>
'''''HEENT'''''<br>
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❑ Modified Mallampati score<br>
❑ Modified Mallampati score<br>


:❑ Class I: Soft palate, uvula, fauces, pillars visible
:❑ Class I: [[Soft palate]], [[uvula]], [[fauces]], [[pillars]] visible


:❑ Class II: Soft palate, uvula, fauces visible
:❑ Class II: [[Soft palate]], [[uvula]], [[fauces]] visible


:❑ Class III: Soft palate, base of uvula present
:❑ Class III: [[Soft palate]], base of [[uvula]] present


:❑ Class IV: Only hard palate visible<br><br>
:❑ Class IV: Only [[hard palate]] visible<br><br>


'''''Cardiothoracic'''''<br>
'''''Cardiothoracic'''''<br>


❑ Auscultation of heart sounds (including number of sounds, pitch, interval, murmurs, gallops, or rubs) over 4 precordial regions in sitting position (stethoscope diaphragm) and auscultation of mitral area while in left lateral decubitus position (stethoscope bell)<br>
❑ Auscultation of heart sounds (including number of sounds, pitch, interval, murmurs, gallops, or rubs) over 4 precordial regions in sitting position (stethoscope diaphragm) and auscultation of [[mitral area]] while in [[left lateral decubitus]] position (stethoscope bell)<br>


:❑ Normal S1 and S2
:❑ Normal S1 and S2
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:❑ Murmur may be physiologic or may suggest valvulopathy or hemodynamic derangement (e.g. anemia)
:❑ Murmur may be physiologic or may suggest valvulopathy or hemodynamic derangement (e.g. anemia)


:❑ Pericardial friction rub may suggest pericarditis<br>
:❑ [[Pericardial friction rub]] may suggest [[pericarditis]]<br>


❑ Point of maximal impulse (PMI) (normally one, non-sustained, tapping impulse per cardiac cycle located less than 2-3 cm from midclavicular line at 5th intercostal space)<br>
[[Point of maximal impulse]] (PMI) (normally one, non-sustained, tapping impulse per cardiac cycle located less than 2-3 cm from [[midclavicular line]] at 5th intercostal space)<br>


❑ Auscultation of anterior and posterior pulmonary regions bilaterally<br>
❑ Auscultation of anterior and posterior [[pulmonic region]]s bilaterally<br>


:❑ Crackles suggest pulmonary edema, which might be attributed to congestive heart failure
:❑ [[Crackle]]s suggest [[pulmonary edema]], which might be attributed to [[congestive heart failure]]


:❑ If pulmonary auscultation abnormal, egophony, tactile fremitus, and thoracic percussion may be needed<br><br>
:❑ If [[pulmonary auscultation]] is abnormal, [[egophony]], [[tactile fremitus]], and [[thoracic percussion]] may be needed<br><br>


'''''Vascular'''''<br>
'''''Vascular'''''<br>


Pulses of both upper extremities (radial, ulnar, brachial) and lower extremities (dorsalis pedis, posterior tibial, popliteal)<br>
[[Pulse]]s of both upper extremities ([[Radial artery|radial]], [[Ulnar artery|ulnar]], [[Brachial artery|brachial]]) and lower extremities ([[dorsalis pedis]], [[posterior tibial]], [[Popliteal artery|popliteal]])<br>


❑ Femoral pulses bilaterally<br>
[[Femoral pulse]]s bilaterally<br>


❑ Femoral auscultation bilaterally for bruits<br>
[[Femoral auscultation]] bilaterally for [[bruit]]s<br>


❑ Modified Allen test bilaterally to evaluate adequacy of radial access<br>
❑ Modified Allen test bilaterally to evaluate adequacy of radial access<br>
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'''''Neurological'''''<br>
'''''Neurological'''''<br>


❑ Upper/lower extremity motor strength<br>
❑ Upper/lower extremity [[motor strength]]<br>


❑ Upper/lower extremity sensory exam<br>
❑ Upper/lower extremity [[sensory exam]]<br>


❑ Spasticity or rigidity<br>
[[Spasticity]] or [[rigidity]]<br>


❑ Deep tendon reflexes<br>
[[Deep tendon reflexes]]<br>


❑ Bilateral Babinski<br>
❑ Bilateral [[Babinski]]<br>


CN assessment<br>
[[Cranial nerves]] assessment<br>
❑ Coordination and [cerebellar exam]]s ([[Finger to nose]], [[Romberg]], [[heel to shin]], [[alternating move]ent])<br>


Coordination and cerebellar exams (Finger to nose, Romberg, Heel to shin, alternating movement)<br>
[[Gait]]</div>}}
 
Gait</div>}}
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{{familytree | | | | | F01 | | | | | | | | | | | | | | | | | | | | | |F01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Provide appropriate counseling before catheterization'''<br><br>
{{familytree | | | | | F01 | | | | | | | | | | | | | | | | | | | | | |F01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Provide appropriate counseling before catheterization'''<br><br>
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''Warfarin''<br>
''Warfarin''<br>


❑ Hold warfarin for at least 2 to 6 days before elective coronary angiography (to prevent bleeding)<br>
❑ Hold [[warfarin]] for at least 2 to 6 days before elective coronary angiography (to prevent bleeding)<br>


❑ Confirm INR < 1.8 (preferable INR < 1.4) within 24 hours before arterial puncture<br>
❑ Confirm [[INR]] < 1.8 (preferable INR < 1.4) within 24 hours before arterial puncture<br>


❑ Restart warfarin 12 to 24 hours following catheterization (warfarin requires 2 to 3 days for INR to become therapeutic range)<br>
❑ Restart [[warfarin]] 12 to 24 hours following catheterization (warfarin requires 2 to 3 days for INR to become therapeutic range)<br>


❑ Consider heparin bridging 3 days before planned catheterization for high risk patients to prevent prolonged subtherapeutic INR<br>
❑ Consider [[heparin bridging]] 3 days before planned catheterization for high risk patients to prevent prolonged subtherapeutic INR<br>


:❑ Therapeutic dose LMWH 1 mg/kg subcutaneously twice daily for high-risk patients who are not at high risk of bleeding
:❑ Therapeutic dose [[LMWH]] 1 mg/kg [[subcutaneous]]ly twice daily for high-risk patients who are not at high risk of bleeding


:❑ Intermediate dose LMWH 40 mg subcutaneously twice daily for high-risk patients at high risk of bleeding<br><br>
:❑ Intermediate dose [[LMWH]] 40 mg [[subcutaneous]]ly twice daily for high-risk patients at high risk of bleeding<br><br>


''Novel Oral Anticoagulants''<br>
''Novel Oral Anticoagulants''<br>


❑ Hold NOAC before catheterization as follow<br>
❑ Hold [[NOAC]] before catheterization as follow<br>


❑ Rivaroxaban: Hold rivaroxaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk<br>
[[Rivaroxaban]]: Hold rivaroxaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk<br>


❑ Apixaban: Hold apixaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk<br>
[[Apixaban]]: Hold apixaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk<br>


❑ If patient does not develop any hematoma, restart NOAC 1 day after the catheterization for patients with low bleeding risk OR 2-3 days after the catheterization for patients with high bleeding risk<br><br>
❑ If patient does not develop any hematoma, restart NOAC 1 day after the catheterization for patients with low bleeding risk OR 2-3 days after the catheterization for patients with high bleeding risk<br><br>
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''Dabigatran''<br>
''Dabigatran''<br>


❑ Hold dabigatran based on renal function as shown below<br>
❑ Hold [[dabigatran]] based on renal function as shown below<br>


:❑ CrCl > 50 ml/min: Hold dabigatran for 1 day if low/intermediate bleeding risk or 3 days if high bleeding risk (e.g. major surgery)
:❑ [[CrCl]] > 50 ml/min: Hold dabigatran for 1 day if low/intermediate bleeding risk or 3 days if high bleeding risk (e.g. major surgery)


:❑ CrCl between 30 and 50 ml/min: Hold dabigatran for 3 days if low/intermediate bleeding risk or 5 days if high bleeding risk (e.g. major surgery)
:❑ CrCl between 30 and 50 ml/min: Hold dabigatran for 3 days if low/intermediate bleeding risk or 5 days if high bleeding risk (e.g. major surgery)
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''LMWH''<br>
''LMWH''<br>


❑ Hold LMWH for 12 hours before cardiac catheterization<br>
❑ Hold [[LMWH]] for 12 hours before cardiac catheterization<br>


❑ Resume LMWH 12-24 hours following cardiac catheterization<br><br>
❑ Resume LMWH 12-24 hours following cardiac catheterization<br><br>
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''Phosphodiesterase inhibitors''<br>
''Phosphodiesterase inhibitors''<br>


❑ Hold sildenafil/tadalafil/vardenafil for at least 2 days before elective coronary angiography<br>
❑ Hold [[sildenafil]]/[[tadalafil]]/[[vardenafil]] for at least 2 days before elective cardiac catheterization<br>


❑ Restart sildenafil/tadalafil/vardenafil one day after catheterization</div>}}
❑ Restart sildenafil/tadalafil/vardenafil one day after catheterization</div>}}
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{{familytree | | | | | G01 | | | | | | | | | | | | | | | | | | | | | |G01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Identify ASA physical status'''<br>
{{familytree | | | | | G01 | | | | | | | | | | | | | | | | | | | | | |G01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Identify ASA physical status'''<br>
❑ 1=Healthy individual with no systemic diseases<br>
❑ 1=Healthy individual with no [[systemic disease]]s<br>


❑ 2=Mild systemic disease<br>
❑ 2=Mild [[systemic disease]]<br>


❑ 3=Severe systemic disease<br>
❑ 3=Severe [[systemic disease]]<br>


❑ 4=Severe systemic disease that poses a constant   threat to the patient’s life<br>
❑ 4=Severe [[systemic disease]] that poses a constant threat to the patient’s life<br>


❑ 5=Moribund patient not expected to survive   without the operation/procedure<br>
❑ 5=[[Moribund patient]] not expected to survive without the operation/procedure<br>


❑ 6=Patient declared brain-dead or whose organs  are being removed for donation</div>}}
❑ 6=Patient declared brain-dead or whose organs  are being removed for donation</div>}}
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{{familytree | | | |,|-|^|-|.| | | | | | | | | | | | | | | | | | | | |}}
{{familytree | | | I01 | | I02 | | | | | | | | | | | | | | | | | | | |I01=ASA physical status ≥ 4|I02=ASA physical status < 4}}
{{familytree | | | I01 | | I02 | | | | | | | | | | | | | | | | | | | |I01=[[ASA physical status]] ≥ 4|I02=[[ASA physical status]] < 4}}


{{familytree | | | |!| | | |!| | | | | | | | | | | | | | | | | | | | |}}
{{familytree | | | |!| | | |!| | | | | | | | | | | | | | | | | | | | |}}
{{familytree | | | J01 | | |!| | | | | | | | | | | | | | | | | | | | |J01=Consult anesthesia}}
{{familytree | | | J01 | | |!| | | | | | | | | | | | | | | | | | | | |J01=Consult [[anesthesia]]}}
{{familytree | | | |`|-|v|-|'| | | | | | | | | | | | | | | | | | | | |}}
{{familytree | | | |`|-|v|-|'| | | | | | | | | | | | | | | | | | | | |}}
{{familytree | | | | | K01 | | | | | | | | | | | | | | | | | | | | | |K01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Perform pre-procedure routine work-up'''<br>
{{familytree | | | | | K01 | | | | | | | | | | | | | | | | | | | | | |K01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Perform pre-procedure routine work-up'''<br>
❑ Complete blood count (CBC)<br>
[[Complete blood count]] (CBC)<br>


❑ Platelet count (Administration of unfractionated heparin, low molecular weight heparinoids, and parenteral glycoprotein 2b3a inhibitors are associated with thrombocytopenia. Thrombocytopenia is a contraindication to the administration of parenteral glycoprotein 2b3a inhibitors)<br>
[[Platelet count]] (Administration of [[unfractionated heparin]], [[low molecular weight heparin]], and parenteral [[glycoprotein 2b3a inhibitor]]s are associated with thrombocytopenia. [[Thrombocytopenia]] is a contraindication to the administration of parenteral glycoprotein 2b3a inhibitors)<br>


❑ Electrolytes panel<br>
[[Electrolytes panel]]<br>


❑ Baseline serum creatinine and BUN. Calculate and record estimated creatinine clearance/eGFR (creatinine clearance/eGFR may significantly be different from true GFR in patients with unstable renal function) <br>
❑ Baseline serum [[creatinine]] and [[BUN]]. Calculate and record estimated [[creatinine clearance]]/[[eGFR]] (creatinine clearance/eGFR may significantly be different from true GFR in patients with unstable [[renal function]]) <br>


❑ Glycemia<br>
[[Glycemia]]<br>


Beta-HCG within 2 weeks of procedure for women of child-bearing age<br>
[[ß-HCG]] within 2 weeks of procedure for women of child-bearing age<br>


❑ Baseline ECG within 24 hours of procedure
❑ Baseline [[ECG]] within 24 hours of procedure


:❑ Assess baseline ischemic changes
:❑ Assess baseline ischemic changes


:❑ Presence of baseline bundle branch block (BBB) (Cardiac catheterization may damage HIS   system and induce BBB)<br>
:❑ Presence of baseline [[bundle branch block]] (BBB) (Cardiac catheterization may damage HIS system and induce BBB)<br>


❑ PT/INR within 24 hours, especially if patient is receiving warfarin (INR > 1.8 is a relative contraindication of cardiac catheterization)<br>
[[PT]]/[[INR]] within 24 hours, especially if patient is receiving [[warfarin]] (INR > 1.8 is a relative contraindication of cardiac catheterization)<br>


❑ CXR if patient suspected to have pulmonary edema or other diseases</div>}}
[[CXR]] if patient suspected to have pulmonary edema or other diseases</div>}}
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{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}}
{{familytree | | | | | L01 | | | | | | | | | | | | | | | | | | | | | |L01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Address relevant and significant comorbidities'''<br><br>
{{familytree | | | | | L01 | | | | | | | | | | | | | | | | | | | | | |L01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Address relevant and significant comorbidities'''<br><br>
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❑ Prolonged INR (>1.8) 24 hours prior to procedure<br>
❑ Prolonged INR (>1.8) 24 hours prior to procedure<br>


:❑ Administer low-dose vitamin K 1-2 mg PO
:❑ Administer low-dose [[vitamin K]] 1-2 mg PO


:❑ Repeat INR and confirm new INR < 1.8 (preferable INR ≤ 1.4). If INR still > 1.8
:❑ Repeat INR and confirm new INR < 1.8 (preferable INR ≤ 1.4). If INR still > 1.8
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::❑ Administer additional vitamin K 2-4 mg PO if anticipated procedure is > 24 hours later. Administer more  doses of low-dose vitamin K (1-2 mg PO) if INR still high
::❑ Administer additional vitamin K 2-4 mg PO if anticipated procedure is > 24 hours later. Administer more  doses of low-dose vitamin K (1-2 mg PO) if INR still high


::❑ Cancel transfemoral approach (except if emergency) if INR does not normalize in time of procedure
::❑ Cancel [[transfemoral approach]] (except if emergency) if INR does not normalize in time of procedure


::❑ Consider transradial approach if radial artery accessible to reduce risk of bleeding
::❑ Consider transradial approach if radial artery accessible to reduce risk of bleeding


::❑ Consider transfusion of fresh frozen plasma (FFP)<br>
::❑ Consider [[transfusion]] of [[fresh frozen plasma]] (FFP)<br>


❑ Renal insufficiency (CrCl < 60 ml/min)<br>
[[Renal insufficiency]] (CrCl < 60 ml/min)<br>


:❑ Saline administration
:❑ [[Saline]] administration


::❑ In patients with no CHF, administer 0.9% or 0.45% normal saline: 1 mL/ kg/ hour (MAX 100 ml/hour) for 12 hours before contrast '''AND''' 12 hours after contrast) in patients with no CHF
::❑ In patients with no [[CHF]], administer 0.9% or 0.45% normal saline: 1 mL/ kg/ hour (MAX 100 ml/hour) for 12 hours before contrast '''AND''' 12 hours after contrast) in patients with no CHF


::❑ In patients with CHF, administer 0.45% normal saline: 0.5 ml/kg/hr (MAX 50 ml/hr) 12 hrs before contrast '''AND''' 12 hours after contrast
::❑ In patients with CHF, administer 0.45% normal saline: 0.5 ml/kg/hr (MAX 50 ml/hr) 12 hrs before contrast '''AND''' 12 hours after contrast


:❑ Consider administration of NaHCO3
:❑ Consider administration of [[sodium bicarbonate]] ([[NaHCO3]])


::❑ Mix 150 mEq of NaHCO3  in 1 liter of D5W in non-diabetic patients OR mix 150 mEq of NaHCO3 in 1 liter of sterile water in diabetic patients.
::❑ Mix 150 mEq of NaHCO3  in 1 liter of D5W in non-diabetic patients OR mix 150 mEq of NaHCO3 in 1 liter of sterile water in [[diabetic patient]]s.


::❑ Administer 3 ml/kg bolus (MAX 300 ml) for 1 hour prior to procedure AND 1 mL/kg/hour (MAX 100 ml/hr) during the procedure AND 1 mg/kg/hour for 6 hours post-procedure
::❑ Administer 3 ml/kg [[bolus]] (MAX 300 ml) for 1 hour prior to procedure AND 1 mL/kg/hour (MAX 100 ml/hr) during the procedure AND 1 mg/kg/hour for 6 hours post-procedure


:❑ Follow-up serum creatinine 2 to 5 days following catheterization<br>
:❑ Follow-up serum creatinine 2 to 5 days following catheterization<br>
Line 485: Line 488:
:❑ Regimen 1
:❑ Regimen 1


::❑ Methylprednisolone 60 mg IV once, '''AND'''
::❑ [[Methylprednisolone]] 60 mg IV once, '''AND'''


::❑ Diphenhydramine 50 mg IV once, '''AND'''
::❑ [[Diphenhydramine]] 50 mg IV once, '''AND'''


::❑ Cimetidine 300 mg (or alternative H2 blocker) IV once
::❑ [[Cimetidine]] 300 mg (or alternative H2 blocker) IV once


:❑ Regimen 2
:❑ Regimen 2


::❑ Prednisolone 50 mg PO at 13 hours, 7 hours, and 1 hour (total of 3 doses) before procedure</div>}}
::❑ [[Prednisolone]] 50 mg PO at 13 hours, 7 hours, and 1 hour (total of 3 doses) before procedure</div>}}
{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}}
{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}}
{{familytree | | | | | M01 | | | | | | | | | | | | | | | | | | | | | |M01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Confirm pre-cath checklist on the day of the procedure'''
{{familytree | | | | | M01 | | | | | | | | | | | | | | | | | | | | | |M01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Confirm pre-cath checklist on the day of the procedure'''
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'''''Antiplatelet therapy'''''<br>
'''''Antiplatelet therapy'''''<br>
''Aspirin''<br>
''Aspirin''<br>
❑ Administer aspirin 325 mg PO once at least 2 hours before any cardiac catheterization procedure<br>
❑ Administer [[aspirin]] 325 mg PO once at least 2 hours before any cardiac catheterization procedure<br>
''Thienopyridine'' should be administered '''ONLY''' when there is intention for PCI or high likelihood to perform PCI during left heart catheterization. Generally, right heart catheterizations do not require administration of thienopyridine <br>
''Thienopyridine''<br>
A [[thienopyridine]] should be administered '''ONLY''' when there is intention for PCI or high likelihood to perform PCI during left heart catheterization. Generally, right heart catheterizations do not require administration of thienopyridine <br>


❑ Administer '''ANY''' of the following thienopyridines at least 2 to 6 hours before the procedure ONLY when there is intention for PCI or high likelihood to perform PCI: <br>
❑ Administer '''ANY''' of the following thienopyridines at least 2 to 6 hours before the procedure ONLY when there is intention for PCI or high likelihood to perform PCI: <br>
:❑ Clopidogrel 600 mg (loading dose) PO once, '''OR'''
:❑ [[Clopidogrel]] 600 mg ([[loading dose]]) PO once, '''OR'''


:❑ Prasugrel 60 mg (loading dose) PO once, '''OR'''
:❑ [[Prasugrel]] 60 mg ([[loading dose]]) PO once, '''OR'''


:❑ Ticagrelor 180 mg (loading dose) PO once<br><br>
:❑ [[Ticagrelor]] 180 mg ([[loading dose]]) PO once<br><br>


'''''Conscious Sedation'''''<br>
'''''Conscious Sedation'''''<br>
Line 590: Line 594:
'''''Consider antihistamine'''''<br>
'''''Consider antihistamine'''''<br>


❑ Consider administration of diphenhydramine (Bendaryl) 25 mg PO once<br><br>
❑ Consider administration of [[diphenhydramine]] ([[Bendaryl]]) 25 mg PO once<br><br>


'''''Consider anti-nausea agents'''''<br>
'''''Consider anti-nausea agents'''''<br>


❑ Consider administration of ondansetron (Zofran) 4 mg IV once</div>}}
❑ Consider administration of [[ondansetron]] ([[Zofran]]) 4 mg IV once</div>}}
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{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}}
{{familytree | | | | | O01 | | | | | | | | | | | | | | | | | | | | | |O01=Transfer patient to cath lab}}
{{familytree | | | | | O01 | | | | | | | | | | | | | | | | | | | | | |O01=Transfer patient to cath lab}}

Revision as of 20:17, 17 April 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Yazan Daaboul, M.D.

Cardiac catheterization pre-procedure evaluation resident survival guide Microchapters
Overview
Classification
Pre-procedure Evaluation
Do's
Don'ts

Overview

Cardiac catheterization is an endovascular procedure that aims to study cardiac function and anatomy, as well as to diagnose and treat acute cardiovascular diseases and evaluate surgical candidates. Cardiac catheterization may be either diagnostic (no intervention) or therapeutic (percutaneous coronary intervention or PCI). However, it may also be classified as coronary angiography (assess patency of coronary arteries), left heart catheterization (to assess blood flow, anatomy, and pressures in left heart chambers and to evaluate the anatomy and function of the mitral and aortic valves), or right heart catheterization (to assess blood flow, anatomy, and pressures in right heart chambers, anatomy and function of the tricuspid and pulmonic valves, pulmonary artery pressure, and pulmonary capillary wedge pressure). Determining emergency/urgency for revascularization dictates how extensive and how thorough the pre-cardiac catheterization management will be. In the case of emergencies (e.g. myocardial infarction), patient transfer to the catheterization laboratory and immediate revascularization (door-to-balloon) precede all other steps in management. In contrast, stable patients require a more extensive work-up pre-catheterization to minimize the risk of adverse events that may develop during or following the procedure.

Classification

Cardiac catheterization may be either:

However, cardiac catheterization may also classified based on the cardiac structure in which the catheter is inserted:

Coronary Angiography

Insertion of the catheter into the coronary arteries. Coronary angiography assesses the patency of coronary arteries.

Left Heart Catheterization

Left heart catheterization (LHC) is the insertion of the catheter into the left ventricle. LHC is used to assess the following:

Right Heart Catheterization

Right heart catheterization (RHC) is the insertion of the catheter into the right ventricle and the pulmonary artery. RHC is used to assess the following:

Cardiac Catheterization Pre-procedure Evaluation

{{familytree | | | | | E01 | | | | | | | | | | | | | | | | | | | | | |E01=
Examine the patient

Vital signs, including BP, HR, RR, T, room air SpO2

Height (in meters), weight (in kilograms), and body mass index (BMI)

❑ Level of consciousness, orientation, and ability to cooperate and communicate

Skin

Xanthelesma or xanthoma (suggestive of dyslipidemia)

Edema (suggestive of renal insufficiency or congestive heart failure)

Acral and/or central cyanosis

HEENT

❑ Head and neck range of motion

❑ Modified Mallampati score

❑ Class I: Soft palate, uvula, fauces, pillars visible
❑ Class II: Soft palate, uvula, fauces visible
❑ Class III: Soft palate, base of uvula present
❑ Class IV: Only hard palate visible

Cardiothoracic

❑ Auscultation of heart sounds (including number of sounds, pitch, interval, murmurs, gallops, or rubs) over 4 precordial regions in sitting position (stethoscope diaphragm) and auscultation of mitral area while in left lateral decubitus position (stethoscope bell)

❑ Normal S1 and S2
❑ S3 may be pathologic or may be a normal finding in young or pregnant
❑ S4 may be pathologic or may be a normal finding in elderly
❑ Murmur may be physiologic or may suggest valvulopathy or hemodynamic derangement (e.g. anemia)
Pericardial friction rub may suggest pericarditis

Point of maximal impulse (PMI) (normally one, non-sustained, tapping impulse per cardiac cycle located less than 2-3 cm from midclavicular line at 5th intercostal space)

❑ Auscultation of anterior and posterior pulmonic regions bilaterally

Crackles suggest pulmonary edema, which might be attributed to congestive heart failure
❑ If pulmonary auscultation is abnormal, egophony, tactile fremitus, and thoracic percussion may be needed

Vascular

Pulses of both upper extremities (radial, ulnar, brachial) and lower extremities (dorsalis pedis, posterior tibial, popliteal)

Femoral pulses bilaterally

Femoral auscultation bilaterally for bruits

❑ Modified Allen test bilaterally to evaluate adequacy of radial access

❑ Carotid auscultation bilaterally

❑ Jugular venous pressure

Neurological

❑ Upper/lower extremity motor strength

❑ Upper/lower extremity sensory exam

Spasticity or rigidity

Deep tendon reflexes

❑ Bilateral Babinski

Cranial nerves assessment
❑ Coordination and [cerebellar exam]]s (Finger to nose, Romberg, heel to shin, [[alternating move]ent])

Gait
}}
 
 
Is cardiac catheterization an emergency?
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
 
No
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Refer to management of acute coronary syndromes
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Confirm that the patient has ANY of the following indications for cardiac catheterization

Left heart catheterization
❑ Canadian cardiovascular society (CCS) class III (i.e. symptoms with everyday living activities) or class IV angina (i.e. inability to perform any activity without angina or angina at rest) despite medical therapy, OR
❑ Angina plus systolic dysfunction, OR
❑ Uncertain diagnosis following non-invasive test and need to confirm diagnosis, OR
Systolic dysfunction with unexplained cause, OR
❑ Survivor of sudden cardiac death, polymorphic VT, or sustained monomorphic VT, OR
❑ Suspected spasm or non-atherosclerotic cause of ischemia, OR
❑ High-risk stress test finding, defined as ANY of following [1]:

❑ Resting LVEF < 35%
❑ High-risk treadmill score (≤ 11)
❑ Severe exercise LVEF < 35%
❑ Stress-induced large perfusion defect
❑ Stress-induced multiple perfusion defects
❑ Large, fixed perfusion defect with LV dilation OR increased lung uptake
LV dilation or increased lung uptake
❑ Stress-induced moderate perfusion defect with LV dilation or increased lung uptake

Right heart catheterization
❑ Patient in shock with unknown volume status
Cardiogenic shock

❑ Diagnosis of follow-up of pulmonary artery hypertension

❑ Patients with advanced cardiopulmonary diseases who require surgery

Left-to-right shunt
Valvular disease
Pulmonary artery hypertension
Congenital heart disease
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Obtain a detailed history

History of Present Illness

Age

Chest pain or chest discomfort

❑ Onset of symptoms

❑ Sensation of heaviness, tightness, pressure, or squeezing

❑ Duration of each episode

❑ Radiation to the left arm, jaw, neck, right arm, back, or epigastrium

❑ Timing of symptoms (morning vs. evening vs. wake patient at night)

Alleviating factors (e.g. medications or rest)

Exacerbating factors

❑ Association of symptoms with food intake

Palpitations

Nausea or vomiting

Sweating

Dyspnea

Orthopnea

Dizziness

Weakness of extremities

Numbness or tingling of extremities

Lightheadedness

Syncope or presyncope

❑ Increased frequency of symptoms

❑ Worsening of severity

❑ Previous episodes

❑ Recent infections

Fever

Weight or appetite changes

Stress

Fatigue

Possible Symptom Triggers

Physical exertion

Air pollution or fine particulate matter

❑ Recent infection

Heavy meal intake

Cocaine

Marijuana

Cardiovascular Risk Factors

❑ Known CAD (review available cardiac catheterizations or CABG reports)

Smoking history

❑ Baseline blood pressure (Duration, antihypertensive therapy, compliance with medications)

❑ History of diabetes mellitus (Duration, DM control, compliance, antidiabetic medications, recent HbA1C, screening for microvascular and macrovascular DM complications)

Dyslipidemia

Obesity (BMI> 30 kg/m2)

Past Medical History

Congenital heart disease

Left to right shunts

Dextrocardia

Situs inversus

❑ History of renal disease (CrCl < 60 mL/min)? Does the patient currently have a stable renal function?

❑ History of bleeding tendency

❑ Known significant anemia (Hct < 30%)

❑ History of heparin-induced thrombocytopenia (HIT)

❑ History of pulmonary disease

❑ History of major surgery in the past month

❑ Anticipated major surgery in the next year

Medications

❑ Prescribed drug

❑ Home oxygen therapy

Over-the-counter drugs

Herbs and supplements

❑ Administration of ANY of the following medications within the last 48 hours prior to catheterization?

Aspirin
Clopidogrel
Prasugrel
Ticagrelor
Metformin
❑ Other oral antidiabetic agents
Insulin injections
Phosphodiesterase inhibitors (e.g. Tadalafil, sildenafil, or vardenafil)
Warfarin. If yes, what is most recent INR?
Unfractionated heparin or Low molecular weight heparin (LMWH). If yes, when was last dose?
❑ Other chronic anticoagualants (e.g. dabigatran, NOACs)

Allergies

❑ List of allergies, including severity and manifestations (pruritus, rash, hives, stridor, or anaphylactic shock)

❑ Known drug allergies

❑ Allergy to aspirin or history of nasal polyps or aspirin desensitization
❑ Allergy to heparin
❑ Allergy to [sedative]]s
❑ Other drug allergies
Contrast allergy
Latex allergy
Allergy to shellfish (controversial association between shellfish allergy and contrast allergy)
❑ Other known environmental and food allergies

Family History

❑ Family history of premature cardiovascular diseases

Social and Sexual History

Healthcare proxy and available family members for patient care

❑ Barrier to tolerate or adhere to dual antiplatelet therapy (DAPT) or follow-up visits

Pregnancy or possible pregnancy

Advanced Directives

DNR status

DNI status
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Provide appropriate counseling before catheterization

❑ Address individual concerns and questions

Hold Food Intake Before Procedure

❑ Keep patient NPO at least 6 hours before elective coronary angiography

Hold Certain Medications Before Procedure

Warfarin

❑ Hold warfarin for at least 2 to 6 days before elective coronary angiography (to prevent bleeding)

❑ Confirm INR < 1.8 (preferable INR < 1.4) within 24 hours before arterial puncture

❑ Restart warfarin 12 to 24 hours following catheterization (warfarin requires 2 to 3 days for INR to become therapeutic range)

❑ Consider heparin bridging 3 days before planned catheterization for high risk patients to prevent prolonged subtherapeutic INR

❑ Therapeutic dose LMWH 1 mg/kg subcutaneously twice daily for high-risk patients who are not at high risk of bleeding
❑ Intermediate dose LMWH 40 mg subcutaneously twice daily for high-risk patients at high risk of bleeding

Novel Oral Anticoagulants

❑ Hold NOAC before catheterization as follow

Rivaroxaban: Hold rivaroxaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk

Apixaban: Hold apixaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk

❑ If patient does not develop any hematoma, restart NOAC 1 day after the catheterization for patients with low bleeding risk OR 2-3 days after the catheterization for patients with high bleeding risk

Dabigatran

❑ Hold dabigatran based on renal function as shown below

CrCl > 50 ml/min: Hold dabigatran for 1 day if low/intermediate bleeding risk or 3 days if high bleeding risk (e.g. major surgery)
❑ CrCl between 30 and 50 ml/min: Hold dabigatran for 3 days if low/intermediate bleeding risk or 5 days if high bleeding risk (e.g. major surgery)

❑ CrCl < 30 ml/min: Hold dabigatran for 2 to 5 days if low/intermediate bleeding risk or > 5 days if high bleeding risk (e.g. major surgery)

❑ If patient does not develop any hematoma, restart dabigatran 1 day after the catheterization for patients with low bleeding risk OR 2-3 days after the catheterization for patients with high bleeding risk

LMWH

❑ Hold LMWH for 12 hours before cardiac catheterization

❑ Resume LMWH 12-24 hours following cardiac catheterization

Metformin

❑ Hold metformin 2 days before elective coronary angiography
❑ Consider holding all other oral antidiabetic agents before elective coronary angiography and administering insulin instead
❑ Consider endocrinology consult for appropriate administration of antidiabetic agents before and after catheterization ❑ Restart metformin (or other oral antidiabetic agents) 2 days post-procedure OR until creatinine is stable (to prevent lactic acidosis and contrast-induced renal failure)

Phosphodiesterase inhibitors

❑ Hold sildenafil/tadalafil/vardenafil for at least 2 days before elective cardiac catheterization

❑ Restart sildenafil/tadalafil/vardenafil one day after catheterization
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Identify ASA physical status

❑ 1=Healthy individual with no systemic diseases

❑ 2=Mild systemic disease

❑ 3=Severe systemic disease

❑ 4=Severe systemic disease that poses a constant threat to the patient’s life

❑ 5=Moribund patient not expected to survive without the operation/procedure

❑ 6=Patient declared brain-dead or whose organs are being removed for donation
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
ASA physical status ≥ 4
 
ASA physical status < 4
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Consult anesthesia
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Perform pre-procedure routine work-up

Complete blood count (CBC)

Platelet count (Administration of unfractionated heparin, low molecular weight heparin, and parenteral glycoprotein 2b3a inhibitors are associated with thrombocytopenia. Thrombocytopenia is a contraindication to the administration of parenteral glycoprotein 2b3a inhibitors)

Electrolytes panel

❑ Baseline serum creatinine and BUN. Calculate and record estimated creatinine clearance/eGFR (creatinine clearance/eGFR may significantly be different from true GFR in patients with unstable renal function)

Glycemia

ß-HCG within 2 weeks of procedure for women of child-bearing age

❑ Baseline ECG within 24 hours of procedure

❑ Assess baseline ischemic changes
❑ Presence of baseline bundle branch block (BBB) (Cardiac catheterization may damage HIS system and induce BBB)

PT/INR within 24 hours, especially if patient is receiving warfarin (INR > 1.8 is a relative contraindication of cardiac catheterization)

CXR if patient suspected to have pulmonary edema or other diseases
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Address relevant and significant comorbidities

❑ Prolonged INR (>1.8) 24 hours prior to procedure

❑ Administer low-dose vitamin K 1-2 mg PO
❑ Repeat INR and confirm new INR < 1.8 (preferable INR ≤ 1.4). If INR still > 1.8
❑ Administer additional vitamin K 2-4 mg PO if anticipated procedure is > 24 hours later. Administer more doses of low-dose vitamin K (1-2 mg PO) if INR still high
❑ Cancel transfemoral approach (except if emergency) if INR does not normalize in time of procedure
❑ Consider transradial approach if radial artery accessible to reduce risk of bleeding
❑ Consider transfusion of fresh frozen plasma (FFP)

Renal insufficiency (CrCl < 60 ml/min)

Saline administration
❑ In patients with no CHF, administer 0.9% or 0.45% normal saline: 1 mL/ kg/ hour (MAX 100 ml/hour) for 12 hours before contrast AND 12 hours after contrast) in patients with no CHF
❑ In patients with CHF, administer 0.45% normal saline: 0.5 ml/kg/hr (MAX 50 ml/hr) 12 hrs before contrast AND 12 hours after contrast
❑ Consider administration of sodium bicarbonate (NaHCO3)
❑ Mix 150 mEq of NaHCO3 in 1 liter of D5W in non-diabetic patients OR mix 150 mEq of NaHCO3 in 1 liter of sterile water in diabetic patients.
❑ Administer 3 ml/kg bolus (MAX 300 ml) for 1 hour prior to procedure AND 1 mL/kg/hour (MAX 100 ml/hr) during the procedure AND 1 mg/kg/hour for 6 hours post-procedure
❑ Follow-up serum creatinine 2 to 5 days following catheterization

❑ Contrast allergy

❑ Administer the following regimen before the procedure (controversial timing)
❑ Regimen 1
Methylprednisolone 60 mg IV once, AND
Diphenhydramine 50 mg IV once, AND
Cimetidine 300 mg (or alternative H2 blocker) IV once
❑ Regimen 2
Prednisolone 50 mg PO at 13 hours, 7 hours, and 1 hour (total of 3 doses) before procedure
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Confirm pre-cath checklist on the day of the procedure

❑ Confirm patient full name
❑ Identify indication for procedure

❑ Planned procedure

❑ Diagnostic cardiac catheterization
❑ Diagnostic cardiac catheterization with possible PCI
❑ PCI

❑ Appropriate history and physical examination documented in patient record

❑ Informed consent is filled within 30 days, complete, signed, and available in patient record

❑ Candidacy for DES

❑ Does the patient have significant anemia (Hct < 30%)
❑ Has the patient had any major surgery in the past month or is anticipating any major surgery in the next year?
❑ Does the patient have clinically overt bleeding?
❑ Is the patient receiving chronic anticoagulation (e.g. warfarin or dabigatran)
❑ Does the patient have a history of medications non-adherence?
❑ Does the patient have someone available to transport to and from the hospital?

❑ Allergies and adverse drug reactions

❑ Contrast allergy. If yes, was the patient pre-treated?
❑ Aspirin allergy. If yes, does the patient need desensitization?
❑ Latex allergy: If yes, remove all latex products from procedural use
❑ Heparin induced thrombocytopenia (HIT): If yes, consider alterative antithrombotic agent
❑ Patient known to have multiple allergies? If yes, did you consider pretreatment?

❑ Medications

❑ Was the patient administered ANY of the following medications within the last 48 hours prior to catheterization?
❑ Aspirin
❑ Clopidogrel
❑ Metformin
❑ Phosphodiesterase inhibitors (e.g. Tadalafil, sildenafil, or similar drugs)
❑ Warfarin. If yes, what the patient’s pre-op (within 48 hours) INR?
❑ Low molecular weight heparin (LMWH). If yes, when was last dose?
❑ Other chronic anticoagualants (e.g. dabigatran, NOACs)

❑ ASA physical status available

❑ Modified mallampati score available

❑ Does patient have any contraindication to sedation?
Sedatives are contraindicated in drug allergy, < 6 hours of NPO for solid food/non-clear liquids, < 2 hours of NPO for clear liquids, abnormal ECG findings, any condition that might compromise airway patency or that would interfere with intubation, hemodynamic instability, or clinically significant comorbidities

❑ Patient's height (in meter) and weight (in kilograms) recorded?
❑ Pre-procedural work-up available AND reviewed (CBC, electrolytes, glycemia, PT/INR, creatinine, BUN, PT/INR within 24 hours if receiving warfarin, ECG within 24 hours, CXR if applicable)

❑ Renal function (serum creatinine, BUN, creatinine clearance/eGFR)
❑ Bleeding risk (anemia, thrombocytopenia, prolonged INR/PT)
❑ Cardiac assessment (ECG)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Administer Preprocedural Drugs

Antiplatelet therapy
Aspirin
❑ Administer aspirin 325 mg PO once at least 2 hours before any cardiac catheterization procedure
Thienopyridine
A thienopyridine should be administered ONLY when there is intention for PCI or high likelihood to perform PCI during left heart catheterization. Generally, right heart catheterizations do not require administration of thienopyridine

❑ Administer ANY of the following thienopyridines at least 2 to 6 hours before the procedure ONLY when there is intention for PCI or high likelihood to perform PCI:

Clopidogrel 600 mg (loading dose) PO once, OR
Prasugrel 60 mg (loading dose) PO once, OR
Ticagrelor 180 mg (loading dose) PO once

Conscious Sedation
Sedatives are contraindicated in drug allergy, < 6 hours of NPO for solid food/non-clear liquids, < 2 hours of NPO for clear liquids, abnormal ECG findings, any condition that might compromise airway patency or that would interfere with intubation, hemodynamic instability, or clinically significant comorbidities
❑ Administer diazepam 5-10 mg PO once
❑ Additional drugs may be administered pre-procedure, but are usually administered once patient is inside the cath lab. These drugs (combination) include:

❑ Fentanyl 25 to 50 microgram IV, AND
❑ Midazolam 1 to 2 mg IV

Consider antihistamine

❑ Consider administration of diphenhydramine (Bendaryl) 25 mg PO once

Consider anti-nausea agents

❑ Consider administration of ondansetron (Zofran) 4 mg IV once
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Transfer patient to cath lab
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Do's

  • Perform a transradial approach instead of a transfemoral appraoach if radial artery is patent
  • Hold anticoagulants, anti-diabetic agents, and phosphodiesterase inhibitors before the procedure
  • Keep patient NPO at least 6 hours before the procedure
  • Prepare the patient before the procedure if he is known to have contrast allergy, renal insufficiency, or diabetes mellitus
  • Administer minimal among of contrast dye before a full injection to ensure the patient is not allergic or to confirm is adequately prepared
  • Maintain the patient in a conscious state when administering sedatives

Don'ts

  • Do not perform right heart catheterization (RHC) for routine management of pulmonary edema
  • Do not perform RHC before a trial of intravascular volume expansion is attempted for low-risk patients
  • Do not perform RHC for patients with certain cardiac tamponade, in whom RHC would delay treatment
  • Do not perform RHC for patients with compensated heart failure undergoing low-risk non-cardiac surgery
  • Do not administer thienopyridine if PCI will not be performed or unlikely to be performed during catheterization
  • Do not remove compressive gauze at the site of injection before 24 hours of catheterization or before the patient is being discharged
  • Do not insert the catheter at an infected site
  • Do not perform catheterization if patient is pregnant (relative contraindication)
  • Do not perform catheterization if the patient has uncontrolled hypertension or uncontrolled glycemia

References

  1. Marso SP, Teirstein PS, Kereiakes DJ, Moses J, Lasala J, Grantham JA (2012). "Percutaneous coronary intervention use in the United States: defining measures of appropriateness". JACC Cardiovasc Interv. 5 (2): 229–35. doi:10.1016/j.jcin.2011.12.004. PMID 22326193.