cardiac, thoracic and vascular Flashcards
thoracic anatomy1) where does the azygous vein run2) where does the thoracic duct run3) where does the phrenic nerve run4) where does the vagus nerve run5) what are the volumes of each lung and and lobes6) what muscles are responsible for quiet inspiration7) what are accessory muscles?8) role of type I and II pneumocytes9) role of pores of Kahn
1) runs along the right side and dumps into superior vena cava2) runs along the right side, crosses midline at T4-5 and dumps into left subclavian vein at junction with internal jugular vein3) runs anterior to hilum4) runs posterior to hilum5) right lung, 3 lobes is 55% volume and left (2 lobes + lingula) is 45%6) diaphragm (80%), intercostals (20%)7)sternocleidomastoid muscle, levators, serratus posterior, scalenes8) Type I pneumocytes-gas exchangeType II pneumocytes- surfactant production9) direct air exchange bw alveoli
Pulmonary Function tests1) what predicted postop FEV1 do you need to be able to resect?-what if it is close, what diagnostic test should you get2) What is DLCO, what does it measure/represent and what does the value depend on3) what predicted postop DLCO is needed for lung resection4) what preop pCO2, pO2 and VO2max are contraindications for lung resection
1) predicted postop FEV1>0.8 needed for resection–if close, get qualitative V/Q scan to see contribution of that portion of lung to overall FEV1. if low may still be able to resect.2) Diffusion capacity of lung for CO-measures carbon monoxide diffusion and represents O2 exchange capacity-value is dependent on capillary surface area, hemoglobin content and alveolar architecture3) >10mL/min/mm HgCO (or >40% predicted postop value)4) pCO2>50, PO2
What is the most common lung surgery that causes1) persistent air leak2) atelectasis3) Arrhythmias
1) wedge/secmentectomy2) lobectomy3) pneumonectomy
Lung Cancer1) T/F: MCC of cancer-related death in US2) what factor has strongest influence on survival3) what is MC site of metastasis (and other met sites)4)T/F: recurrence usually appears as single metastasis5) what disease stages are resectable6) possible surgeries7) prognosis8) MC type of lung CA9) Most malignant Lung CA
1) True2) node involvement3) Brain (liver, other lung, supraclavicular nodes, adrenals)4) False- usually disseminated metastases5) Stage I and II are resectable, T3N1M0 (stage IIIa) may be resectable6) lobectomy or pneumonectomy MC, sample suspicious nodes7) poor. 10% 5-year overall survival. 30% with resection for cure8) non-small cell carcinoma, adenocarcinoma is MC overall type9) mesothelioma
Non-small cell carcinoma of lung1) what % of all lung CA2) what type is more centrally located3) what type is more peripherally located4) chemo- when to use and which drugs
1)80%2) squamous cell CA3) adenocarcinoma (MC)4) Stage II or higher- carboplatin, Taxol (can also do XRT)
Small cell lung CA1) what % of lung CA2) prognosis3) 5-year survival rate for T1N0M04) rx5) cell origin
1) 20%2) poor, <5% 5-year survival3) 50%4) most just get chemo-XRT (cisplatin, etoposide)5) neuroendocrine
TNM staging for lung CA1) difference bw T1-T42) difference bw N1-N3 and significance for treatment3) difference bw stage 1-IV4) single best test to determine T and N status5) single best test to determine M status
1) T1 is 3cm but >2cm from carina; T3-invades chest wall, pericardium, diaphragm or
Paraneoplastic syndromes associated with1) squamous cell CA2) small cell lung CA3) which paraneoplastic syndrome is MC
1) PTH-related peptide2) ACTH and ADH3) ACTH
Mesothelioma1) prognosis2) risk factor
1) most malignant lung CA–> aggressive local invasion, nodal invasion and distant mets common at diagnosis2) asbestos exposure
Mediastinoscopy1) what lung tumors should you use it for?2) what does it not assess3) where are you looking with it?a-right-side structuresb- left-side structuresc-anterior structures
1) centrally located tumors and pts with suspicious adenopathy2) aorto-pulmonary window nodes (L-lung drainage)3) middle mediastinuma-azygous vein and SVCb- Recurent laryngeal nerve, esophagus, aorta, main pulmonary arteryc-innominate artery and vein, right pulm artery
What is the Chamberlain procedure and what does it assess
goes through left 2nd rib cartilage (anterior thoracotomy or parasternal mediastinotomy) to assess the AP window nodes (L-lung drainage)
What is Bronchoscopy used to assess for lung CA
needed for centrally located tumors to check for airway invasion
2 criteria needed for operative resection of lung CA
pts must be 1) operable (appropriate FEV1 and DLCO values)2) resectable (no T4, N2, N3 or M disease)
Pancoast tumor1) where is it?2) related symptoms/syndromes
1) invades apex of chest wall–>2) Horner’s syndrome (invasion of sympathetic chain-> ptosis, miosis, anhidrosis) or ulnar nerve compression
Coin lesion on CXR1) how many are malignant overall and by age2) what findings suggest benign disease3) If suspicious what is next step
1) 10% malignant overall (<5% in pts younger than 50yo but 50% in pts older than 50yo)2) no growth in 2 years, smooth contour3) guided bx or wedge resection
1) Asbestos exposure increases lung CA risk by what %2) appearance of bronchoalveolar CA3) treatment of lung metastasis from other primary
1) 90%2) can look like pneumonia, grows along alveolar walls, multifocal3) can resect if isolated and not associated with any other systemic disease for colon, renal cell, sarcoma, melanoma, ovarian and endometrial CA
Carcinoids of lung1) cell type and location2) % with mets, % with symptoms3) pronosis for typical and atypical carcinoid4) rx5) tumor characteristics that result in increased recurrence
1) Neuroendocrine tumor, centrally located usually2) 5% have mets and 50% have sx at time of dx3) typical has 90% 5-yr survival, atypical is only 60%4) resection, treat like CA5) recurrence increased with positive nodes or tumors>3cm (outcome closely linked to histology)
Bronchial Adenomas1) types and malignant potential2) which types are slow growing and don’t metastasize3) which types spread along perineural lymphatics4) which types are very XRT sensitive5) rx for each type6) which type can have 10-yr survival with unresectable disease
1) mucoepidermoid adenoma, mucous gland adenoma and adenoid cystic adenoma (all are malignant)2, 5) Mucoepidermoid adenoma and mucous gland adenoma (rx-resection)3, 4, 5) Adenoid cystic adenoma-slow growing (rx- resection, if unresectable, XRT is good palliation). Can get 10-yr survival with unresectable disease
Hamartomas1) malignant potential2) CT appearance3) dx and rx
1) benign (MC benign adult lung tumor)2) calcifications and appear as popcorn lesion3) dx made with CT- repeat chest CT in 6 months to confirm, no resection needed
Mediastinal tumors in adults1) MC presentation/sx2) MC type in adults and children3) what % of symptomatic mediastinal masses are malignant4) what % of asymptomatic mediastinal masses are benign5) MC site for mediastinal tumor6) Anterior tumors7) Middle mediastinal tumors8) posterior tumors
1) asx. however, can have CP, cough, dyspnea2) neurogenic tumors (usually posterior)3) 50%; 4) 90%5) thymus (anterior)6) Thymus- thymoma (#1 anterior mediastinal mass in adults), thyroid CA and goiters, T-cell lymphoma, Teratoma (and other germ-cell tumors), paraThyroid adenomas7) heart, trachea, ascending aorta- bronchogenic, paricardial and enteric cysts, lymphoma8) esophagus and descending aorta-enteric cysts, neurogenic tumors, lymphoma
Thymoma1) rx2) 50% rule3) what % of pts with Myasthenia gravis have thymoma
1) resect (also resect thymus if too big or refractory M.G.)2) 50% have symptoms, 50% have M.G., 50% are malignant3) 10%
Myasthenia Gravis1) sx and cause2) rx
1) fatigue, weakness, diplopia, ptosis, caused by antibodies to acetylcholine receptors2) anticholinesterase inhibitors (neostigmine), steroids, plasmapheresis. 80% get improvement with thymectomy (including those who don’t have a thymoma)
Mediastinal Germ Cell Tumors1) how to dx2) MC one in mediastinum3) MC malignant one in mediastinum4) Teratoma-a) benign or malignant?b) rx5) Seminomaa) tumor markersb) rx6) Non-seminomaa) tumor markersb) rx
1) biopsy (often with mediastinoscopy)2) Teratoma3) Seminoma4) a- can be eitherb- resection, possible chemo5) a-10% are beta-HCG positive. should NOT have AFPb-XRT (extremely sensitive) , chemo only if mets or bulky nodal disease, surgery for residual dz after that6)a-90% have AFP and beta-HCG elevationb-chemo (cisplatin, bleomycin, VP-16), surgery for residual disease
Mediastinal cysts1) Bronchiogenica-locationb-rx2) Pericardiala-locationb-rx
1)a-posterior to carina; b-resect2) a-right costophrenic angle; b-leave alone (benign)
Neurogenic Mediastinal tumors1) sx2) rx3) what % have intraspinal involvement requiring simultaneous spinal surgery4) what type is MC5) what type produces catecholamines and is associated with von Recklinghausen’s disease6) 2 other types of tumors
1) pain, neurologic deficit2) resection3) 10%4) Schwannoma (Neurolemmoma)5) Paraglanglioma6) Neurofibroma, neuroblastoma
Trachea1) benign tumor in adults2) benign tumor in children3) malignant tumor4) MC early complication after tracheal surgery and rx5) MC late complication after tracheal surgery
1) papilloma2) hemangioma3) squamous cell carcinoma4) laryngeal edema. rx- intubate, recemic epi and steroids5) granulation tissue formation
Trachea1) post-intubation stenosisa- where does it occur with tracheostomy and ET tubeb- rx2) Tracheo-innominate artery fistula- a-when does it occurb- rxc- how to avoid this complication3) Tracheoesophageal fistulaa-when does it occurb- temporary treatmentc- permanent treatment
1) a-at stoma site with tracheostomy and at cuff site with ET tubeb- if minor- serial dilation, bronchoscopic resection or laser ablationif severe or recurring- tracheal resection with end-to-end anastamosis2) a- with tracheostomy-> can have rapid exsanguinationb-place finger in trach hole and hold pressure–> median sternotomy with ligation and resection of innominate arteryc- keep tracheostomy above 3rd tracheal ring3) a-with prolonged intubationb- place large-volume cuff endotracheal tube below fistula, attempt repair after vent weanc-tracheal resection and reanastamosis; close hole in esophagus; sternohyoid flap between esophagus and trachea
Lung Abscess1) MC cause and location2) rx3) how to differentiate from empyema
1) aspiration, superior segment of RLL2) abx alone (95% success); if that fails- CT-guided drainage. Surgery if above fails or can’t r/o CA (>6cm, doesn’t resolve within 6month)3) can get CT scan
Empyema1) MC cause2) symptoms3) characteristics of pleural fluid labs4) empyema phases- time when it is seen and rxa)exudative phaseb) Fibro-proliferative phasec) organized phase
1) pneumonia and subsequent paraneumonic effusion (staph or strep) is MC. but also can be 2/2 esophageal, pulm or mediastinal surgery2) pleuritic CP, fever, cough, SOB3) WBCs >500cells/cc, bacteria and + gm stain4) a)1st week. rx- abx, CTb) 2nd week. rx- CT, abx; possible VATS deloculation (=video-assisted thoracoscopic surgery)c) 3rd week. rx- decrotication (fibrous peel occurs around lung). some use intra-pleural tPA to dissolve the peel. May need Eloesser flap (open thoracic windo direct to external environment) to frail/elderly
Chylothorax1) fluid appearance and lab findings and special stain2) infection risk3) MC causes4) causes of L-sided chylothorax vs right-sided chylothorax5) rx
1) white, milky fluid. has inc lymphocytes and TAGs (triglycerides >110ml/uL). Sudan red stains fat2) resistant to infection= no risk3) trauma or iatrogenic injury 50%malignancy (ie-lymphoma 2/2 tumor burden in lymphatics) 50%4) Injury above T5/6-> left-sided chylothoraxInjury below-> right sided chylothorax5) 2-3 wks conservative rx (Chest tube, octreotide, low-fat diet/TPN)-if fails and cause is trauma-> ligation of thoracic duct on right side in low mediastinum-if fails and cause is malignant-> need talc pleurodesis and possible chemo &/or XRT
Massive Hemoptysis1) quantity that defines it2) MC site of bleed3) MC cause4) MCC of death5) rx
1) >600cc/24hr2) high pressure bronchial arteries3) 2/2 infection4) asphyxiation5) place bleeding side down; mainstem intubation to opposite side of bleed. rigid bronchoscopy to identify site and possible control of beed. May need lobectomy/pneumonectomy or bronchial artery embolization if not suitable for surgery
Spontaneous pneumothorax1) classic patient description2) MC side3) recurrence risk4) rx for all5) when to operate and what operation
1) thin, tall, healthy young male2) right side MC3) after 1st pneumo-20%, after 2nd-60%, after 3rd-80%4) Chest tube5) if recurrence, air leak >7 days, non-reexpansion, high-risk profession (airline pilot, diver, mountain climber) or pt living in remote area– do thoracoscopy, apical blebectomy and mechanical pleurodesis
Other lung conditions1) MCC of arrest after blunt trauma2) occurs in temporal relation to menstruation 2/2 to endometrial implants in visceral lung pleura3) rx of residual hemothorax despite 2 good chest tubes4) when to surgically drain clotted pneumothorax5) cause of broncholiths6) MCC of mediastinitis
1) tension pneumo 2/2 impaired venous return2) Catamenial pneumothorax3) OR for thorascopic drainage4) if >25% of lung, air-fluid levels or signs of infection (fever, inc WBCs). do surgery in 1st week to avoid peel5) infection6) usually occurs after cardiac surgery
Management of whiteout on CXR if1) midline shift toward whiteout2) midline shift away from whiteout3) no shift
1) most likely collapse-> need bronchoscopy to remove plug2) most likely effusion-> place CT3) CT scan to figure out
Bronchiectasis1) causes2) surgical management
1) acquired from infection, tumor or cystic fibrosis2) too diffuse for surgery
TB1) MC location in lungs2) typical pathology3) what is a Ghon complex4) Rx5) difference between path in sarcoidosis and TB
1) apical2) calcifications and caseating granulomas3) parenchymal lesion + enlarged hilar LNs4) INH, rifampin, pyrazinamide5) has non-caseating granulomas
1) Rx of recurrent pleural effusions2) rx of airway fires3) MC benign Chest wall tumor4) MC malignant chest wall tumor
1) mechanical pleurodesis (Talc powder for malignancies)2) usually from laser. 3) osteochondroma4) chondrosarcoma
Lung AVMS1) vasculature involved2) MC location3) what syndrome can they occur with4) rx5) sx
1) cnxn bw pulm artery and veins2) lower lobes3) osler-Weber-rendu disease4) embolization5) hemoptysis, SOB, neurologic events
Congenital Heart disease1) a)what kind of shunt results in cyanosisb) why does squatting relive symptoms in these ptsc) what is Eisenmenger’s syndrome and why does it occurd) complications of cyanosis2) what kind of shunt causes CHF3) 3 causes of L-> R shunts and how do they present4) 1 cause of R->L shunt
1) a) R->L shuntb) squatting-> increased SVR and decrease R->L shuntc) shift from L-> R to R->L shunt. 2/2 increased pulmonary vascular resistance (PVR) and pulmonary HTN, generally irreversibled)polycythemia, strokes, brain abscess, endocarditis2) L-> R shunt3) VSD, ASD, PDA. manifest as failure to thrive, inc HR, tachypnea, hepatomegaly (1st sign of CHF in children)4) tetralogy of fallot
Congenital Heart disease1) what is the ductus arterios2) What is the ductus venosum3) what provides fetal circulation to placenta (supply deoxygenated blood from fetus to placenta)4) what provides fetal circulation away from placenta (supplies oxygenated blood to fetus)5) MC congenital heart defect6) MC congenital heart defect that results in cyanosis
1) connection bw left PA and descending aorta (blood shunted away from lungs in utero)2) Cnxn bw portal vein and IVC (blood shunted away from liver in utero)3) 2 x umbilical arteries4) umbilical vein (only 1 vein, but 2 arteries)5) VSD6) tetrology of fallot
Ventricular Septal Defect1) direction of shunt2) what % close spontaneously and by what age3) when do they cause symptoms and physiology of why4) consequent symptoms/effects5) Medical rx6) when to repaira)large VSD (Shunt >2.5)b) medium VSD (Shunt 2-2.5)c) what is MC reason for earlier repair
1) L->R2) 80% spontaneously close by 6mo3) large VSDs cause symptoms at 4-6weeks bc of PVR decreasing and shunt increasing4) CHF (tachypnea, tachycardia) and failure to thrive5) diuretics and digoxin6) a- at 1 year old; b-at 5 years old; c- failure to thrive
Atrial Septal Defect1) shunt direction2) what is MC type and location3) what type can have mitral valve and tricuspid valve problems and what syndrome do you see this type with4) when do symptoms occur and what are they5) medical rx6) when to repair
1) L->R2) Ostium secundum, centrally located, 80%3) ostium primum (or Atrioventricular defects or endocardial cushion defects) seen with DOwn’s syndrome4) when shunt >2-> CHF (SOB, recurrent infections). In adults can get paradoxical emboli5) diuretics and digoxin6) 1-2years of age. If canal defects 3-6mo.
Tetrology of Fallot1) shunt direction2) what defects are part of this3) medical rx4) usual timing of repair5) how is repair done
1) R->L2) anterior superior displacement of infundibular septim->pulm artery stenosis and VSD, over-riding aorta, and RV hypertrophy (secondary occurance)3) B-blockers4) 3-6months5) removal of RV outflow tract obstruction (RVOT) and RVOT enlargement + VSD repair
Patent Ductus Arteriosus1) direction of shunt2) what drug causes the PDA to close, and during what timeframe is this successful3) repair of persistent PDA through what type of incision
1) L-> R2) indomethacin, rarely effective beyond the neonatal period3) requires surgical repair through left thoracotomy
Adult Cardiac Disease: Coronary Artery disease1) risk factors2) medical treatment3) branches of Left Main coronary artery4) where are most stherosclerotic lesions5) what is the restenosis rate of drug-eluting stent at 1 year6) what is saphenous vein graft 5-year patency rate7) what is the best conduit for CABG- name the artery, where it branches off of and what it collateralizes with8) Indictions for CABG9) high mortality risk factors for CABG
1) smoking, HTN, male, family hx, hyperlipidemia, diabetes2) nitrates, smoking cessation, weight loss, statins, ASA3) Left anterior descending and Left circumflex arteries4) proximal5) 20% restenosis at 1-year6) 80% patency at 5-years7) internal mammary (branch of subclavian artery) collateralizes with superior epigastric artery8) >70% stenosis for most areas except >50% stenosis for Left main disease is considered significant.CABG for:-Left main >50% stenosis-3-vessel disease (LAD, Cx, and Right Coronary Artery)-2-vessel disease involving LAD-lesions not amenable to stenting9) pre-op cardiogenic shock is #1 risk factor, emergency operations, age, low EF
Complications of MI1) Ventricular Septal Rupturea-symptomsb-timeframe in which occursc- shunt direction and consequent O2 content effectd-how to dxe- rx2) Papillary muscle rupturea- syptomsb-when it occursc-dxd-rx
1)a- hypotension, pansystolic murmurb-usually 3-7d after MIc- L-> R shunt-> increase in pulmonary artery and right atrium O2 contentd- echoe- temporize with intra-aortic balloon pump, patch over septum2) a- hypotension and severe mitral regurgb- 3-7 days after MIc-echod- temporize with IABP, valve replacement
Adult Cardiac disease1) what is MC cause of death in US2) MC valve lesion3) MC benign tumor of the heart and where are they located4) MC malignant heart tumor5) MC metastatic tumor to the heart6) which veins have lowest O2 tension of any tissue in the body and why7) what is the treatment for coming off cardiopulmonary bypass and aortic root vent when blood is dark and aortic perfusion cannula blood is red8) with mediastinal bleeding after a cardiac procedure when do you need to re-explore9) risk-factors for mediastinitis and rx
1) Coronary Artery disease2) aortic stenosis3) myxoma- 75% in LA4) Angiosarcoma5) lung CA6) coronary veins 2/2 O2 extraction by myocardium7) ventilate the lungs8) >500cc for 1st hour, or >250cc/h for 4 hours-> need to re-explore9) obesity, use of bilateral internal mammary arteries, DM. rx- debridement with pectoralis flaps (can also use omentum)
Superior Vena Cava symdrome1) sx2) MC cause and rx
1) upper extremity and face swelling2) MC 2/2 to lung CA invading SVC-> emergent XRT
Post-pericardiotomy syndrome1) sx2) EKG findings3) rx
1) pericardial friction rub, fever, chest pain, SOB2) diffuse ST-segment elevation in mult leads3) NSAIDS, steroids*basically like pericarditis
Endocarditis1) sx2) MC site of prosthetic valve infections3) MC site of native valve infections4) MC organism responsible5) what is MC side except for in which pts6) MC organism in IVDA7) Rx and indications for surgery (how often is medical rx successful)
1) fever, chills, sweats2) Aortic valve3) Mitral Valve4) staph aureus responsible for 50%5) Left side MC (mitral valve) except in IVDA (tricuspid valve)6) pseudomonas7) medical therapy 1st- sucessful in 75%, sterilizes valve in 50%surgery if- failure of abx, severe valve failure or perivalvular abscesses, pericarditis