cardiac, thoracic and vascular Flashcards
thoracic anatomy
1) where does the azygous vein run
2) where does the thoracic duct run
3) where does the phrenic nerve run
4) where does the vagus nerve run
5) what are the volumes of each lung and and lobes
6) what muscles are responsible for quiet inspiration
7) what are accessory muscles?
8) role of type I and II pneumocytes
9) role of pores of Kahn
1) runs along the right side and dumps into superior vena cava
2) runs along the right side, crosses midline at T4-5 and dumps into left subclavian vein at junction with internal jugular vein
3) runs anterior to hilum
4) runs posterior to hilum
5) 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, scalenes
8) Type I pneumocytes-gas exchange
Type II pneumocytes- surfactant production
9) direct air exchange bw alveoli
Pulmonary Function tests
1) what predicted postop FEV1 do you need to be able to resect?
- what if it is close, what diagnostic test should you get
2) What is DLCO, what does it measure/represent and what does the value depend on
3) what predicted postop DLCO is needed for lung resection
4) 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 architecture
3) >10mL/min/mm HgCO (or >40% predicted postop value)
4) pCO2>50, PO2
What is the most common lung surgery that causes
1) persistent air leak
2) atelectasis
3) Arrhythmias
1) wedge/secmentectomy
2) lobectomy
3) pneumonectomy
Lung Cancer
1) T/F: MCC of cancer-related death in US
2) what factor has strongest influence on survival
3) what is MC site of metastasis (and other met sites)
4) T/F: recurrence usually appears as single metastasis
5) what disease stages are resectable
6) possible surgeries
7) prognosis
8) MC type of lung CA
9) Most malignant Lung CA
1) True
2) node involvement
3) Brain (liver, other lung, supraclavicular nodes, adrenals)
4) False- usually disseminated metastases
5) Stage I and II are resectable, T3N1M0 (stage IIIa) may be resectable
6) lobectomy or pneumonectomy MC, sample suspicious nodes
7) poor. 10% 5-year overall survival. 30% with resection for cure
8) non-small cell carcinoma, adenocarcinoma is MC overall type
9) mesothelioma
Non-small cell carcinoma of lung
1) what % of all lung CA
2) what type is more centrally located
3) what type is more peripherally located
4) chemo- when to use and which drugs
1) 80%
2) squamous cell CA
3) adenocarcinoma (MC)
4) Stage II or higher- carboplatin, Taxol (can also do XRT)
Small cell lung CA
1) what % of lung CA
2) prognosis
3) 5-year survival rate for T1N0M0
4) rx
5) cell origin
1) 20%
2) poor, <5% 5-year survival
3) 50%
4) most just get chemo-XRT (cisplatin, etoposide)
5) neuroendocrine
TNM staging for lung CA
1) difference bw T1-T4
2) difference bw N1-N3 and significance for treatment
3) difference bw stage 1-IV
4) single best test to determine T and N status
5) 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 with
1) squamous cell CA
2) small cell lung CA
3) which paraneoplastic syndrome is MC
1) PTH-related peptide
2) ACTH and ADH
3) ACTH
Mesothelioma
1) prognosis
2) risk factor
1) most malignant lung CA–> aggressive local invasion, nodal invasion and distant mets common at diagnosis
2) asbestos exposure
Mediastinoscopy 1) what lung tumors should you use it for? 2) what does it not assess 3) where are you looking with it? a-right-side structures b- left-side structures c-anterior structures
1) centrally located tumors and pts with suspicious adenopathy
2) aorto-pulmonary window nodes (L-lung drainage)
3) middle mediastinum
a-azygous vein and SVC
b- Recurent laryngeal nerve, esophagus, aorta, main pulmonary artery
c-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 tumor
1) 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 CXR
1) how many are malignant overall and by age
2) what findings suggest benign disease
3) 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 contour
3) guided bx or wedge resection
1) Asbestos exposure increases lung CA risk by what %
2) appearance of bronchoalveolar CA
3) treatment of lung metastasis from other primary
1) 90%
2) can look like pneumonia, grows along alveolar walls, multifocal
3) can resect if isolated and not associated with any other systemic disease for colon, renal cell, sarcoma, melanoma, ovarian and endometrial CA
Carcinoids of lung
1) cell type and location
2) % with mets, % with symptoms
3) pronosis for typical and atypical carcinoid
4) rx
5) tumor characteristics that result in increased recurrence
1) Neuroendocrine tumor, centrally located usually
2) 5% have mets and 50% have sx at time of dx
3) typical has 90% 5-yr survival, atypical is only 60%
4) resection, treat like CA
5) recurrence increased with positive nodes or tumors>3cm (outcome closely linked to histology)
Bronchial Adenomas
1) types and malignant potential
2) which types are slow growing and don’t metastasize
3) which types spread along perineural lymphatics
4) which types are very XRT sensitive
5) rx for each type
6) 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
Hamartomas
1) malignant potential
2) CT appearance
3) dx and rx
1) benign (MC benign adult lung tumor)
2) calcifications and appear as popcorn lesion
3) dx made with CT- repeat chest CT in 6 months to confirm, no resection needed
Mediastinal tumors in adults
1) MC presentation/sx
2) MC type in adults and children
3) what % of symptomatic mediastinal masses are malignant
4) what % of asymptomatic mediastinal masses are benign
5) MC site for mediastinal tumor
6) Anterior tumors
7) Middle mediastinal tumors
8) posterior tumors
1) asx. however, can have CP, cough, dyspnea
2) 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 adenomas
7) heart, trachea, ascending aorta- bronchogenic, paricardial and enteric cysts, lymphoma
8) esophagus and descending aorta-enteric cysts, neurogenic tumors, lymphoma
Thymoma
1) rx
2) 50% rule
3) 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 malignant
3) 10%
Myasthenia Gravis
1) sx and cause
2) rx
1) fatigue, weakness, diplopia, ptosis, caused by antibodies to acetylcholine receptors
2) anticholinesterase inhibitors (neostigmine), steroids, plasmapheresis. 80% get improvement with thymectomy (including those who don’t have a thymoma)
Mediastinal Germ Cell Tumors
1) how to dx
2) MC one in mediastinum
3) MC malignant one in mediastinum
4) Teratoma-
a) benign or malignant?
b) rx
5) Seminoma
a) tumor markers
b) rx
6) Non-seminoma
a) tumor markers
b) rx
1) biopsy (often with mediastinoscopy)
2) Teratoma
3) Seminoma
4) a- can be either
b- resection, possible chemo
5) a-10% are beta-HCG positive. should NOT have AFP
b-XRT (extremely sensitive) , chemo only if mets or bulky nodal disease, surgery for residual dz after that
6)a-90% have AFP and beta-HCG elevation
b-chemo (cisplatin, bleomycin, VP-16), surgery for residual disease
Mediastinal cysts 1) Bronchiogenic a-location b-rx 2) Pericardial a-location b-rx
1) a-posterior to carina; b-resect
2) a-right costophrenic angle; b-leave alone (benign)
Neurogenic Mediastinal tumors
1) sx
2) rx
3) what % have intraspinal involvement requiring simultaneous spinal surgery
4) what type is MC
5) what type produces catecholamines and is associated with von Recklinghausen’s disease
6) 2 other types of tumors
1) pain, neurologic deficit
2) resection
3) 10%
4) Schwannoma (Neurolemmoma)
5) Paraglanglioma
6) Neurofibroma, neuroblastoma
Trachea
1) benign tumor in adults
2) benign tumor in children
3) malignant tumor
4) MC early complication after tracheal surgery and rx
5) MC late complication after tracheal surgery
1) papilloma
2) hemangioma
3) squamous cell carcinoma
4) laryngeal edema. rx- intubate, recemic epi and steroids
5) granulation tissue formation
Trachea 1) post-intubation stenosis a- where does it occur with tracheostomy and ET tube b- rx 2) Tracheo-innominate artery fistula- a-when does it occur b- rx c- how to avoid this complication 3) Tracheoesophageal fistula a-when does it occur b- temporary treatment c- permanent treatment
1) a-at stoma site with tracheostomy and at cuff site with ET tube
b- if minor- serial dilation, bronchoscopic resection or laser ablation
if severe or recurring- tracheal resection with end-to-end anastamosis
2) a- with tracheostomy-> can have rapid exsanguination
b-place finger in trach hole and hold pressure–> median sternotomy with ligation and resection of innominate artery
c- keep tracheostomy above 3rd tracheal ring
3) a-with prolonged intubation
b- place large-volume cuff endotracheal tube below fistula, attempt repair after vent wean
c-tracheal resection and reanastamosis; close hole in esophagus; sternohyoid flap between esophagus and trachea
Lung Abscess
1) MC cause and location
2) rx
3) how to differentiate from empyema
1) aspiration, superior segment of RLL
2) 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
Empyema
1) MC cause
2) symptoms
3) characteristics of pleural fluid labs
4) empyema phases- time when it is seen and rx
a) exudative phase
b) Fibro-proliferative phase
c) organized phase
1) pneumonia and subsequent paraneumonic effusion (staph or strep) is MC. but also can be 2/2 esophageal, pulm or mediastinal surgery
2) pleuritic CP, fever, cough, SOB
3) WBCs >500cells/cc, bacteria and + gm stain
4) a)1st week. rx- abx, CT
b) 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
Chylothorax
1) fluid appearance and lab findings and special stain
2) infection risk
3) MC causes
4) causes of L-sided chylothorax vs right-sided chylothorax
5) rx
1) white, milky fluid. has inc lymphocytes and TAGs (triglycerides >110ml/uL). Sudan red stains fat
2) resistant to infection= no risk
3) trauma or iatrogenic injury 50%
malignancy (ie-lymphoma 2/2 tumor burden in lymphatics) 50%
4) Injury above T5/6-> left-sided chylothorax
Injury below-> right sided chylothorax
5) 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 Hemoptysis
1) quantity that defines it
2) MC site of bleed
3) MC cause
4) MCC of death
5) rx
1) >600cc/24hr
2) high pressure bronchial arteries
3) 2/2 infection
4) asphyxiation
5) 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 pneumothorax
1) classic patient description
2) MC side
3) recurrence risk
4) rx for all
5) when to operate and what operation
1) thin, tall, healthy young male
2) right side MC
3) after 1st pneumo-20%, after 2nd-60%, after 3rd-80%
4) Chest tube
5) 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 conditions
1) MCC of arrest after blunt trauma
2) occurs in temporal relation to menstruation 2/2 to endometrial implants in visceral lung pleura
3) rx of residual hemothorax despite 2 good chest tubes
4) when to surgically drain clotted pneumothorax
5) cause of broncholiths
6) MCC of mediastinitis
1) tension pneumo 2/2 impaired venous return
2) Catamenial pneumothorax
3) OR for thorascopic drainage
4) if >25% of lung, air-fluid levels or signs of infection (fever, inc WBCs). do surgery in 1st week to avoid peel
5) infection
6) usually occurs after cardiac surgery
Management of whiteout on CXR if
1) midline shift toward whiteout
2) midline shift away from whiteout
3) no shift
1) most likely collapse-> need bronchoscopy to remove plug
2) most likely effusion-> place CT
3) CT scan to figure out
Bronchiectasis
1) causes
2) surgical management
1) acquired from infection, tumor or cystic fibrosis
2) too diffuse for surgery
TB
1) MC location in lungs
2) typical pathology
3) what is a Ghon complex
4) Rx
5) difference between path in sarcoidosis and TB
1) apical
2) calcifications and caseating granulomas
3) parenchymal lesion + enlarged hilar LNs
4) INH, rifampin, pyrazinamide
5) has non-caseating granulomas
1) Rx of recurrent pleural effusions
2) rx of airway fires
3) MC benign Chest wall tumor
4) MC malignant chest wall tumor
1) mechanical pleurodesis (Talc powder for malignancies)
2) usually from laser.
3) osteochondroma
4) chondrosarcoma
Lung AVMS
1) vasculature involved
2) MC location
3) what syndrome can they occur with
4) rx
5) sx
1) cnxn bw pulm artery and veins
2) lower lobes
3) osler-Weber-rendu disease
4) embolization
5) hemoptysis, SOB, neurologic events
Congenital Heart disease
1) a)what kind of shunt results in cyanosis
b) why does squatting relive symptoms in these pts
c) what is Eisenmenger’s syndrome and why does it occur
d) complications of cyanosis
2) what kind of shunt causes CHF
3) 3 causes of L-> R shunts and how do they present
4) 1 cause of R->L shunt
1) a) R->L shunt
b) squatting-> increased SVR and decrease R->L shunt
c) shift from L-> R to R->L shunt. 2/2 increased pulmonary vascular resistance (PVR) and pulmonary HTN, generally irreversible
d) polycythemia, strokes, brain abscess, endocarditis
2) L-> R shunt
3) VSD, ASD, PDA. manifest as failure to thrive, inc HR, tachypnea, hepatomegaly (1st sign of CHF in children)
4) tetralogy of fallot
Congenital Heart disease
1) what is the ductus arterios
2) What is the ductus venosum
3) 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 defect
6) 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 arteries
4) umbilical vein (only 1 vein, but 2 arteries)
5) VSD
6) tetrology of fallot
Ventricular Septal Defect
1) direction of shunt
2) what % close spontaneously and by what age
3) when do they cause symptoms and physiology of why
4) consequent symptoms/effects
5) Medical rx
6) when to repair
a) large VSD (Shunt >2.5)
b) medium VSD (Shunt 2-2.5)
c) what is MC reason for earlier repair
1) L->R
2) 80% spontaneously close by 6mo
3) large VSDs cause symptoms at 4-6weeks bc of PVR decreasing and shunt increasing
4) CHF (tachypnea, tachycardia) and failure to thrive
5) diuretics and digoxin
6) a- at 1 year old; b-at 5 years old; c- failure to thrive
Atrial Septal Defect
1) shunt direction
2) what is MC type and location
3) what type can have mitral valve and tricuspid valve problems and what syndrome do you see this type with
4) when do symptoms occur and what are they
5) medical rx
6) when to repair
1) L->R
2) Ostium secundum, centrally located, 80%
3) ostium primum (or Atrioventricular defects or endocardial cushion defects) seen with DOwn’s syndrome
4) when shunt >2-> CHF (SOB, recurrent infections). In adults can get paradoxical emboli
5) diuretics and digoxin
6) 1-2years of age. If canal defects 3-6mo.
Tetrology of Fallot
1) shunt direction
2) what defects are part of this
3) medical rx
4) usual timing of repair
5) how is repair done
1) R->L
2) anterior superior displacement of infundibular septim->pulm artery stenosis and VSD, over-riding aorta, and RV hypertrophy (secondary occurance)
3) B-blockers
4) 3-6months
5) removal of RV outflow tract obstruction (RVOT) and RVOT enlargement + VSD repair
Patent Ductus Arteriosus
1) direction of shunt
2) what drug causes the PDA to close, and during what timeframe is this successful
3) repair of persistent PDA through what type of incision
1) L-> R
2) indomethacin, rarely effective beyond the neonatal period
3) requires surgical repair through left thoracotomy
Adult Cardiac Disease: Coronary Artery disease
1) risk factors
2) medical treatment
3) branches of Left Main coronary artery
4) where are most stherosclerotic lesions
5) what is the restenosis rate of drug-eluting stent at 1 year
6) what is saphenous vein graft 5-year patency rate
7) what is the best conduit for CABG- name the artery, where it branches off of and what it collateralizes with
8) Indictions for CABG
9) high mortality risk factors for CABG
1) smoking, HTN, male, family hx, hyperlipidemia, diabetes
2) nitrates, smoking cessation, weight loss, statins, ASA
3) Left anterior descending and Left circumflex arteries
4) proximal
5) 20% restenosis at 1-year
6) 80% patency at 5-years
7) internal mammary (branch of subclavian artery) collateralizes with superior epigastric artery
8) >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 stenting
9) pre-op cardiogenic shock is #1 risk factor, emergency operations, age, low EF
Complications of MI 1) Ventricular Septal Rupture a-symptoms b-timeframe in which occurs c- shunt direction and consequent O2 content effect d-how to dx e- rx 2) Papillary muscle rupture a- syptoms b-when it occurs c-dx d-rx
1)a- hypotension, pansystolic murmur
b-usually 3-7d after MI
c- L-> R shunt-> increase in pulmonary artery and right atrium O2 content
d- echo
e- temporize with intra-aortic balloon pump, patch over septum
2) a- hypotension and severe mitral regurg
b- 3-7 days after MI
c-echo
d- temporize with IABP, valve replacement
Adult Cardiac disease
1) what is MC cause of death in US
2) MC valve lesion
3) MC benign tumor of the heart and where are they located
4) MC malignant heart tumor
5) MC metastatic tumor to the heart
6) which veins have lowest O2 tension of any tissue in the body and why
7) what is the treatment for coming off cardiopulmonary bypass and aortic root vent when blood is dark and aortic perfusion cannula blood is red
8) with mediastinal bleeding after a cardiac procedure when do you need to re-explore
9) risk-factors for mediastinitis and rx
1) Coronary Artery disease
2) aortic stenosis
3) myxoma- 75% in LA
4) Angiosarcoma
5) lung CA
6) coronary veins 2/2 O2 extraction by myocardium
7) ventilate the lungs
8) >500cc for 1st hour, or >250cc/h for 4 hours-> need to re-explore
9) obesity, use of bilateral internal mammary arteries, DM. rx- debridement with pectoralis flaps (can also use omentum)
Superior Vena Cava symdrome
1) sx
2) MC cause and rx
1) upper extremity and face swelling
2) MC 2/2 to lung CA invading SVC-> emergent XRT
Post-pericardiotomy syndrome
1) sx
2) EKG findings
3) rx
1) pericardial friction rub, fever, chest pain, SOB
2) diffuse ST-segment elevation in mult leads
3) NSAIDS, steroids
* basically like pericarditis
Endocarditis
1) sx
2) MC site of prosthetic valve infections
3) MC site of native valve infections
4) MC organism responsible
5) what is MC side except for in which pts
6) MC organism in IVDA
7) Rx and indications for surgery (how often is medical rx successful)
1) fever, chills, sweats
2) Aortic valve
3) Mitral Valve
4) staph aureus responsible for 50%
5) Left side MC (mitral valve) except in IVDA (tricuspid valve)
6) pseudomonas
7) medical therapy 1st- sucessful in 75%, sterilizes valve in 50%
surgery if- failure of abx, severe valve failure or perivalvular abscesses, pericarditis