Pathology Review

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Pathology Review LindseyJones

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Pathology

Transcript of Pathology Review

  • Pathology Review

    LindseyJones

  • Emphysema

    Defined: Abnormal condi-tion of the alveoli result-ing destruction and lossof elasticity.

    Information Gathering

    Visual AssessmentCyanosisBarrel chestAccessory muscle useDigital clubbing of the nail bedsSignificant history of smoking and/or occupational exposure to smoke or other

    pulmonary irritant

    Bedside (Patient Contact) AssessmentDyspnea

    Basic Laboratory AssessmentChest X-rayincreased AP Diameter, flattened diaphragms, hyperlucency,

    diminished pulmonary markings.CBCpolycythemia, increased WBC due to possible infection.ABGsCompensated respiratory acidosis (high PaCO2, normal pH), moderate to

    severe hypoxemia.Sputum cultureoften positive for bacteria.

    Special AssessmentsPFTflows are decreased especially middle sized airways (FEF 25-75%) and FEV1

    Decision Making

    Oxygen therapylow FIO2 (0.24 to 0.28) or 1 to 2 lpm nasal cannula

    Oxygen conserving devices such as liquid oxygen or trans-tracheal oxygen

    Home care education on devices and equipment cleaning

    Rehabilitation efforts (specifics not usually required)

    Aids to help quit smoking such as nicotine replacement therapy

    Bronchodilation medication via MDI or aerosol nebulizers

    What to expect

    You will usually be tempted toutilize high FIO2 because of theseverity of the hypoxemia. Youmay also be tested with an emer-gency, the only time it is appropri-ate to use 100% oxygen on achronically obstructed patient.

    There are usually two obstructivesimulations on the exam and theyare not extremely challenging.

  • Chronic Bronchitis

    Defined: Condition wherethe patient has a produc-tive cough 25% of theyear for at least two con-secutive years

    Information Gathering

    Visual AssessmentProductive cough, purulent sputum productionExposure to pulmonary irritants, like history of smokingFrequent infections

    Bedside (Patient Contact) AssessmentDyspnea

    Basic Laboratory AssessmentChest X-raycould be normal, or may show hyperlucency, diminished \

    pulmonary markings.CBCpossibly increased WBC due to possible infection.ABGscould be normal or very slight respiratory acidosis and hypoxemia

    Special AssessmentsPFTflows are decreased especially middle sized airways (FEF 25-75%) and

    FEV1

    Decision Making

    Anything that promotes good pulmonary hygiene such as chest physiotherapy, hydrationtherapy when sputum is thick.

    Fluid therapy if dehydrated.

    Oxygen therapy for hypoxemia

    Aerosolized bronchodilator therapy

    Antibiotic Tetracycline may be preferable

    What to expectThe most distinguishing charac-

    teristic is that the cough is produc-tive and has been so for a good

    portion of the year.

  • Bronchiectasis

    Defined: Abnormal condi-tion where the bronchisecrete large volumes ofpus during abnormal dila-tion

    Information Gathering

    Visual AssessmentProductive cough, often with bloodDigital clubbing of the nail bedsSignificant history if infections (recurrent)

    Bedside (Patient Contact) AssessmentDyspnea

    Basic Laboratory AssessmentChest X-raygenerally normalSputum culturegram negative bacteria

    Special AssessmentsBronchogram is the primary test. Characterized as a tree in winter pattern

    Decision Making

    Anything that promotes good pulmonary hygiene such as chest physiotherapy, hydrationtherapy when sputum is thick.

    Fluid therapy if dehydrated.

    Oxygen therapy for hypoxemia

    Aerosolized bronchodilator therapy

    May have consider surgical intervention on some highly affected segments

    What to expect

    Central to this is the Bronchogramdiagnostic test. Usually, you willbe told of the suspicion of Bron-chiectasis.

    Increasingly less common on thetest

  • Obstructive Sleep Apnea

    Defined: the cessation ofbreathing during sleep.Is usually obstructive innature but sometimescan be central or a com-bination of the two(mixed).

    Information Gathering

    Visual AssessmentSpouse or bed partner will complain of snoring and will often report witnessing

    periods of apnea that exceed 10 seconds.Excessive upper airway tissue, obesity, thick neckAbility to fall asleep quickly

    Bedside (Patient Contact) AssessmentDyspneaFrequent urination during sleeping hours

    Basic Laboratory AssessmentABGscould be normal or very slight respiratory acidosis and hypoxemia

    Special AssessmentsPolysomnography (Sleep study) - determines if obstructive or centralIf no nasal flow AND no chest movementthen CENTRAL sleep apneaIf no nasal flow WITH chest movementthen OBSTRUCTIVE sleep apnea

    Decision Making

    If central, ventilatory stimulant medication may be used

    If obstructive, use of CPAP or BiPAP is usually initially indicated with follow-up weightloss or upper airway tissue removal through surgery.

    Problem must be corrected immediately, so even if discharging, send devices home withpatient. In the absence of a titration study, initially ordered pressure should be 10 to 20 cmH20.

    What to expectThis is still somewhat rare on the

    test but it does show up.

    It is important to remember toavoid sending the patient home

    without some sort of ventilatorysupport.

  • Asthma

    Defined: Abnormal con-striction of the bronchialsresulting in sputum pro-duction and narrowedairways.

    Information Gathering

    Visual AssessmentAccessory muscle useTachycardia

    Bedside (Patient Contact) AssessmentDyspneaWheezingCongested coughWet, clammy skin

    Basic Laboratory AssessmentABGspossible respiratory acidosis, could be hypoxicChest X-rayhyperinflation, scattered infiltrates, flattened diaphragms.In allergic cases, may see elevated eosinophil count which can cause yellow sputum

    Special AssessmentsPFTDecreased flows in FEV1 but diffusion is normal as manifested by DLCO

    Decision Making

    Oxygen therapy for hypoxemia

    Aerosolized bronchodilator therapy

    Xanthine medication given IV (Aminophylline, etc)

    Promote pulmonary hygiene

    Corticosteroids such as oral or IV prednisone

    What to expect

    When doing PFTs, always do apre and post bronchodilator study.Consider effective if 15% or moreimprovement is noted.

    There are no significant traps inthis simulation except that thepatient may be unresponsive tobronchodilators. In such a case,you are dealing with Status Asth-maticus. Refer to that disease

  • Status Asthmaticus

    Defined: Asthma that willnot respond to bron-chodilation therapy, usu-ally persists more than24 hours.

    Information Gathering

    Visual AssessmentHistorically non-responsive to bronchodilators. Patient will report the need to

    take many bronchodilator treatments before feeling better.Accessory muscle use and retractionsDyspneaWheezingCongested coughWet, clammy skin

    Bedside (Patient Contact) AssessmentPulses paradoxus

    Basic Laboratory AssessmentABGspossible respiratory acidosis when tiring, alkalosis at first due to anxiety,

    could be hypoxicChest X-rayhyperinflation, scattered infiltrates, flattened diaphragms.

    Special Assessments

    Decision Making

    May deteriorate quickly, so if progression is shown, intubate, mechanically ventilate be-fore full ventilatory failure.

    Use subcutaneous epinephrine1 mL of 1:1000 strength. May need to give every 20minutes for up to three consecutive doses

    What to expectThis simulation will challenge

    your ability to recognize impend-ing ventilatory failure. It is veryimportant that you treat it before

    full ventilatory failure.

    There is a frequent need to repeatactions in this simulation which

    will make you uncomfortable. Donot be afraid to administer several

    bronchodilators in succession.The same is true of the subcutane-

    ous epinephrine. If you give onedose, you will likely have to give

    another, and possibly another.Continue if symptoms show no

    signs of relief.

  • Myasthenia Gravis

    Defined: Neuromuscularabnormality where mus-cles experience paralysisstarting from the headdown to the feet includ-ing ventilatory muscles.

    Information Gathering

    Visual AssessmentMay have a history of Myasthenia Gravis if not the onsetDroopy facial muscles and eyelids (Ptosis)

    Bedside (Patient Contact) AssessmentPatient will describe slowly feeling weakness generally but feels better with rest.Double vision (diplopia)Dysphagia (difficulty swallowing)Shrinking Vt, VC, MIP

    Basic Laboratory Assessment

    Special AssessmentsTensilon Challenge Testpositive for Myasthenic crisis if improvement is noted

    upon the administration of Tensilon

    Decision Making

    If Tensilon improves condition then, anticholinesterase therapy is indicated including:

    Neostigmine (prostigmine)Mestinon (pyridostigmine)

    Ok to do additional Tensilon challenge test to observe progression.

    If symptoms improve with Tensilon and then worsen, the must reverse the anticholinesterasewith Atropine.

    Always monitor spontaneous ventilatory volumes (Vt and VC) as well as MIP.

    Never treat Myasthenia gravis with Tensilononly use to diagnose. Use the above men-tioned drugs to provide maintenance.

    Be totally prepared to intubate and mechanically ventilate prior to Tensilon challenge since itcould take out the respiratory drive

    When VC falls off rapidly (especially if below 1.0 L) , then intubate and mechanically venti-late.

    What to expect

    This can be a very tricky simula-tion and it is likely that it willshow up on the exam. Especiallyimportant is your use of Tensilonto diagnose it and an understand-ing of the dangerous affects itcould have. Must always be pre-pared to assume ventilation.

    Vt, VC, and MIP are key in moni-toring this patient for degradationin ventilatory status. Intubateprior to full failure if possible.

  • Drug Overdose

    Defined: Potential loss ofventilatory drive as a re-sult of drug overdose(usually a narcotic)

    Information Gathering

    Visual AssessmentHistorical drug use as told by previous admissions or familySometimes poor self-hygiene, emaciated

    Bedside (Patient Contact) AssessmentLook and act sleepy, difficult to arouseRespiratory rate and pattern is low and/or shallow

    Basic Laboratory AssessmentABGoften show pure respiratory acidosis and/or ventilatory failure

    Special Assessments

    Decision Making

    #1 priority in this case is intubation to protect the airway, prevent aspiration of stomachcontents, and facilitate manual ventilation.

    If narcotic overdose (usually is) then use narcotic reversing medication such a Narcan(Nalaxon)

    Support ventilation until drugs are out of system.

    What to expectThe most important part of this

    simulation is the need for immedi-ate intubation while recognizing

    that there may not be a need tomechanically ventilate until venti-

    latory status deteriorates.

  • Other Neuromuscular

    Defined: Other neuro-muscular diseases orstates include Poliomyeli-tis, Tetanus, Musculardystrophy, and evenbotulism poisoning.

    Information Gathering

    Visual AssessmentHistory of illness

    Bedside (Patient Contact) AssessmentShrinking Vt, VC, MIP

    Basic Laboratory Assessment

    Special Assessments

    Decision Making

    Monitor for ventilatory failure generally through Vt, VC, MIP and ABGs

    What to expect

    If faced with these diseases, sim-ply apply general respiratorymonitoring principles and facili-tate ventilation when needed.

    These are somewhat rare.

  • Head Trauma

    Defined: Potential loss ofventilatory drive as a re-sult of drug overdose(usually a narcotic)

    Information Gathering

    Visual AssessmentSometimes trauma is visual with blood contusions on the headHistory is trauma related, often automobile accident

    Bedside (Patient Contact) AssessmentLook and act sleepy, difficult to arouseRespiratory rate and pattern is low and/or shallow and irregularPupillary response to light may be unequal or inadequate

    Basic Laboratory Assessment

    Special AssessmentsIf intracranial pressure monitor is in place, may see ICP greater than 20

    cm H2O

    Decision Making

    Must constrict vessels in the head by keeping PaCO2 between 25-30 mm Hg.

    Adjust FIO2 to maintain high normal levels (PaO2 of 100 mm Hg).

    Avoid increased ICP by minimizing PEEP usage.

    Suction only when needed due to elevating peak pressures.

    Avoid anything that will increase mean arterial pressure (MAP).

    Sedation is important, but should monitor exhaled volumes and pressures closely

    Use of drugs such as Manitol (cerebral diuretic medication) when ICP is above 20 cm H20

    Use Dilantin and establish an airway if seizure activity is observed

    What to expectUnique to this simulation is the

    need to monitor ICP readings andavoid anything that increases

    MAP. You will likely need tosuction this patient to keep peak

    pressures down but the very act ofdoing so my elevate ICPs.

  • Chest Trauma

    Defined: May any traumaleading to fractured ribsor flail chest

    Information Gathering

    Visual AssessmentCircumstantial history (motor vehicle accident, etc)Respiratory rate and pattern is fast and shallow due to painMay have obvious trauma (bruising) on chest wall

    Bedside (Patient Contact) AssessmentSharp chest pain, especially at the top of each breathParadoxical chest movement if ribs are broken in two places (flail chest)Pneumothorax is possible (see signs and symptoms of pneumothorax)

    Basic Laboratory AssessmentChest x-raymay reveal broken ribs, usually isolated in same area

    Special Assessments

    Decision Making

    Anything that encourages deep (adequate) breathing in spite of pain such as IPPB, incentivespirometry, coughing.

    Watch for ventilatory fatigue and eventual ventilatory failure

    Mechanically support ventilation when it is evident ventilatory failure is impending. If possi-ble do not wait until full ventilatory failure.

    Treat partial pneumothorax if greater than 20% - ie insert chest tubesTreat hemothorax, with chest tubes or thoracentesisTreat tension pneumothorax with a large-bore needle

    What to expect

    This case is usually easy to recog-nize. You may be tempted byoptions that address the brokenribs when, in fact, you simplyneed to address ventilation.

    Very commonly, this case willlead to pneumothorax or partialpneumothorax or hemothorax.

  • Hemothorax/Pneumothorax

    Defined: Loss of adher-ence of the lung to thepleural wall causing thespace to be filled with airor fluid (bloody).

    Information Gathering

    Visual AssessmentRapid and shallow respirations

    Bedside (Patient Contact) AssessmentPercussion: hyperresonant if pneumothorax, dull if hemothoraxTracheal shift: to affected side if pneumothorax, away if tension pneumothoraxSevere dyspneaVery diminished or absent breath soundsPulses paradoxes

    Basic Laboratory AssessmentChest x-raydefinitiveshow hyperlucency, tracheal or mediastinal shift

    Special Assessments

    Decision Making

    Usual treatment is insertion of chest tubesUpper anterior chest tube placement for pneumothorax (involving air)Lower chest tube placement for hemothroax (involving blood and body fluid)

    Treat partial pneumothorax if greater than 20% - ie insert chest tubes

    Treat hemothorax, with chest tubes or thoracentesis

    Treat tension pneumothorax with a large-bore needle

    What to expectPneumothorax, hemothorax, ten-

    sion pneumothorax occurs veryfrequently on the exam

    May include the troubleshootingof chest tube drainage devices

  • Thoracic Surgery

    Defined: Can have vari-ety of complications fromthroacic surgery

    Information Gathering

    Visual Assessment

    Bedside (Patient Contact) AssessmentAlways monitoring chest tube drainage adequacyLooking for potential complications:

    Hypovolemic shock, low hemodynamic values including blood pressureSubcutaneous emphysemaElevated ventilatory pressures

    Basic Laboratory AssessmentChest x-rayto confirm proper re-inflation of the lung and proper placement

    of chest tubes

    Special Assessments

    Decision Making

    Anything that promotes expansion of the lungs including incentive spirometry, IPPB, andpositive pressure mechanical ventilation

    If a lobectomy or pneumonectomy, ventilatory volumes should set lower

    Fluid therapy if volume is a problem (often is).

    What to expect

    Your ability to deal with and trou-bleshoot chest tube maintenance istested in this simulation.

    Sometimes this case is combinedwith chest trauma.

  • Neck/Spinal Injury

    Defined: Any traumathreatening the physicalstructure of the neck.Can include neck or spi-nal surgery.

    Information Gathering

    Visual AssessmentHistorical relevance, some sort of accident such as diving, automobile.Visible damage to the neckAltered conscious levelPulse must be palpated brachially or femorally

    Bedside (Patient Contact) AssessmentVt, VC, PEFR, and other ventilatory volumes may quickly deteriorate

    Basic Laboratory AssessmentNeck x-raywill show injury

    Special Assessments

    Decision Making

    Always be prepared to quickly assist and/or promote ventilation.

    If intubation is required, always use MODIFIED jaw thrust.

    If given option, always intubate with a bronchoscope so damage can be visualized andcare can be taken to avoid inflicting further damage.

    Alternatively, a blind nasal intubation is acceptable.

    What to expectYour knowledge of special intuba-

    tion techniques is what is beingtested in this type of simulation.

  • Abdominal Surgery

    Defined: Surgery of inthe abdominal area forvarious reasons.

    Information Gathering

    Visual AssessmentAll general visual assessments

    Bedside (Patient Contact) AssessmentAll general beside assessment including all vitals

    Basic Laboratory AssessmentVentilatory volumes (VC, Vt, FEV1) compared to pre-surgery baselines

    Special Assessments

    Decision Making

    Establishing baselines in pulmonary function testing flows and volumes.

    Start patient on incentive spirometry prior to surgery, every hour after surgery

    Use positive pressure (IPPB) if needed after surgery if patient is unconscious.

    What to expect

    Abdominal surgery is usually avery general, non-complicatedcase involving preventative careand follow up.

  • Adult Respiratory Distress Syndrome

    Defined: A condition thatresults in significantlydecrease lung compli-ance and consequentprofound hypoxemia

    Information Gathering

    Visual AssessmentRecord may show a variety of insults to the lung including massive surgery,

    near drowning, inhalation of gasoline, hypothermia, and others.Rapid respiratory rateCyanosis

    Bedside (Patient Contact) AssessmentDecreased lung compliance as manifested by increased plateau pressures

    (decreasing static compliance)

    Basic Laboratory AssessmentABGspersistent hypoxemia in spite of elevated FIO2 (may be refractory)Chest x-rayshow granular, or ground glass, or reticulogranular, or honeycomb

    patterns. Often accompanied by diffuse infiltrates.

    Special AssessmentsAll hemodynamic values could deteriorate when positive ventilatory pressures

    become significant.

    Decision Making

    As positive pressure is required increasingly, negative effects may be seen. All should bedone to minimize the mean pressure being put on the pulmonary system, while trying tobalance the need to ventilate with higher pressures an utilize PEEP to maintain oxygena-tion.

    If underlying cause in know, treat it.

    After emergency situation is past, keep FIO2 at 0.6 and use PEEP

    Keep increasing PEEP until an obvious degradation in hemodynamic values is witnessed.

    As ventilatory pressure get higher, OK to consider alternate methods of ventilation includ-ing pressure control, high frequency, etc

    What to expectARDS can be a very disquieting

    case to deal with. Usually persis-tent increases in PEEP are needed.Do not be afraid to increase PEEP

    significantly.

    Also, most often, cardiac outputor some other hemodynamic value

    will fall indicating a need to de-crease PEEP in spite of profound

    hypoxemia.

  • Laryngectomy

    Defined: Surgery done toaddress or remove can-cer of the larynx.

    Information Gathering

    Visual AssessmentSurgical record : Surgery radical (entire larynx) or simple (cord removal)Medical history will show cancer in upper airway

    Bedside (Patient Contact) AssessmentSigns of airway obstruction after surgery. Usually caused by blood within a few

    hours after the surgery.

    Basic Laboratory Assessment

    Special Assessments

    Decision Making

    If radical surgery (entire larynx removed) then the tracheostomy become permanent.

    If not radical then a temporary laryngectomy tube is placed but must be replaced in 3 to 6weeks.

    Prevent aspiration ! Wait at least a week before oral ingestion of liquid and longer for food.Thorough pulmonary hygiene through suctioning

    Use cool aerosol or ultrasonic nebulizer to keep secretions thin and hydrated.

    Once the surgery is done, you can no longer, orally intubate the patient. Even if temporarylaryngectomy tube is in place, you must intubate and/or ventilate through that tube !

    What to expect

    In this case, you are always look-ing for post-surgical complica-tions like blood clots in the laryn-geal tube. Often, you will have tomechanically ventilate this patientthrough the laryngectomy tube.

  • Guillain-Barre Syndrome

    Defined: An insidiousneuromuscular probleminvolving muscle paraly-sis. Paralysis begins inthe lower extremities andmoves upward, includingthe ventilatory muscles.

    Information Gathering

    Visual AssessmentMedical history or patient complaint of recent fluenza-type sickness.

    Bedside (Patient Contact) AssessmentComplaint of sluggish lower extremitiesShrinking Vt, VC, MIP

    Basic Laboratory AssessmentABGsimpending or current ventilatory failure.

    Special AssessmentsSpinal tapwill show increased protein in the spinal fluid

    Decision Making

    Be primarily concerned with loss of ventilation, monitor ventilatory volumes (VC, Vt) andMIP.

    Be patient about intubation and mechanical ventilation. Onset can be slow.

    Primary treatment will involve mechanical ventilation and letting the syndrome run itscourse.

    What to expectLike most neuromuscular cases,you will be tested in your ability

    to recognize deterioration in venti-latory muscles. In this case, onset

    can be slow, so dont jump-the-gun and mechanically ventilate

    too early. Only do so as VC fallsbelow 1.0 L.

    Otherwise, you will be manipulat-ing the ventilator and possibly

    weaning.

  • Shock

    Defined: Condition wheretissues oxygenation is injeopardy due to a suddendecrease in blood flow.

    Information Gathering

    Visual AssessmentHistorical evidence of an event or massive trauma or hypothermia, etcGeneral appearancecold, clammy, dusky, cyanoticTachycardia, tachypnea

    Bedside (Patient Contact) AssessmentHypotensiveTemperature may be below normalReduction in urine output

    Basic Laboratory AssessmentABGshypoxemia and ventilatory failure

    Special AssessmentsReduction in common hemodynamic values (CVP, PAP, PCWP) and cardiac output.

    Decision Making

    Mechanically ventilate with ventilatory failure.

    Oxygen is key. Start it as evidence of shock is presented.

    Use oxygen at least 40% but may use up to 100%

    Main treatment involved treating the original problem (that which caused the shock). Thiscan be highly variable.

    What to expect

    Shock will test your ability torecognize it and monitor the pa-tient for ventilatory failure. Mostof the simulation is dealing withtypical ventilatory considerationssuch as ventilator manipulation.

  • Heart Surgery

    Defined: Any kind of sur-gery on the heartInformation Gathering

    Visual AssessmentDo well rounded assessment prior to surgery including vital signs, family history

    of cardiac illness.

    Bedside (Patient Contact) AssessmentPreoperative assessments of breath soundsBaseline data including basic spirometry of all types including FEV1/FVC and

    pre and post bronchodilator studies

    Basic Laboratory AssessmentABGspreoperative for baseline

    Special Assessments

    Decision Making

    Always assess ventilatory volumes and be prepared to mechanically ventilate

    Incentive spirometry every hour after surgery for lung expansion and alveolar ventilation.

    If unable (unconscious) use simple ventilatory assisting devices such as IPPB or CPAPwith mask.

    Be on the alert for cardiac arrestperform CPR without reservation or consideration ofthe heart surgery.

    What to expectThis case is not too complicated.You may feel hesitant to do CPRon someone fresh out of surgery.

    Just do it.

  • Pulmonary Edema / CHF

    Defined: Significant re-duction in cardiac output.Involvement of fluidpenetrating the alveolarcapillary membrane intothe lungs.

    Information Gathering

    Visual AssessmentHistory of CHF or pulmonary hypertensionTachypnea, tachycardia, anxiety

    Bedside (Patient Contact) AssessmentCold, clammy, diaphoreticPink frothy secretionsEdema of fluids (especially pedal edema)Pitting edema (+2, +3)Breath sounds reveal fine, wet rales

    Basic Laboratory AssessmentABGsventilatory failure with moderate to severe hypoxemiaChest X-rayButterfly pattern, fluffy infiltrates

    Special AssessmentsIncreased hemodynamic pressure (PCWP, PAP, CVP)

    Decision Making

    Treat as an emergency !

    100% oxygen

    Administer diuretic medication furosemide (Lasix)

    Cardiac intatropic stimulating drugs such as digoxin, digitalis if increased PCWP and PAP

    Be prepared to treat ventilatory failure with mechanical ventilation

    What to expect

    This case may feel complicatedbecause it involves the heart andhemodynamic values. It is usuallyeasily identified by pink frothysecretions and butterfly pattern onthe chest X-ray.

    You may need to make the dis-tinction between pulmonaryedema caused by cardiac prob-lems and that which is caused byalveolar capillary membrane prob-lems (ARDS). If it is cardiac,then you must treat the heart.

  • Myocardial Infarction/Arrhythmia

    Defined: Ischemia to theheart causing muscledamage and potentialfailure.

    Information Gathering

    Visual AssessmentHistory of chest pain, radiating pain down the left armFamily history of diseaseDiaphoreticHistory of nauseaTachycardia

    Bedside (Patient Contact) AssessmentCold, diaphoretic and clammy to the touchDyspnea

    Basic Laboratory AssessmentABGshypoxemiaECG (EKG) - pronounced Q waves and S-T segment elevation

    Special AssessmentsCardiac enzymes including CPK, LDH, SGOT are elevated

    Decision Making

    Emergency100% oxygen.

    Oxygen at adult therapeutic level (40 to 60 %) upon suspicion or first presentation so signsand/or symptoms

    Treat arrhythmias

    Bradycardia with Atropine or IsuprelPVCs with lidocaine or oxygenPulseless ventricular tachycardia with defibrillationVentricular Fibrillation with defibrillation

    Note: For Ventricular fibrillation, defibrillate at ascending watt/sec or joule settings360 joulesrepeat as neededDo not exceed 360 joules

    Note: For Atrial fibrillation or flutter, do synchronized cardioversionstart at 50 joules

    What to expectWill likely need to treat arrhyth-

    mias with appropriate medicationand/or defibrillation

  • Pulmonary Emboli

    Defined: Situation wherethe pulmonary artery be-comes obstructed anddead-space ventilationresults. Sometimescalled deadspace dis-ease.

    Information Gathering

    Visual AssessmentHistory of recent major surgery or trauma (amputations, clotted massive bleeding

    sights)Complaint of chest pain and dyspnea

    Bedside (Patient Contact) AssessmentElevated vitals including pulse, respirations, and blood pressureBreath sounds - wheezing and medium ralesPECO2 (Capnography) decreasing PECO2 during normal PaCO2

    Basic Laboratory AssessmentABGspersistent hypoxemia in spite of increasing FIO2

    Special AssessmentsV/Q scan will ventilation without adequate perfusion

    Decision Making

    Anticoagulation therapy with Heparin or CoumadinNote: must monitor clotting tests

    PTT for HeparinPT for Coumadin

    Clot-busting medication such as steptokinase. May also use a bolus of heparin

    Mechanical ventilation as needed.

    Emergency level oxygen100%

    What to expect

    This case primarily involves rec-ognizing the pulmonary emboliand treating it with anticoagula-tion medications. You will likelyhave to monitor clotting times,PTT or PT.

    Otherwise, involves general respi-ratory therapy.

  • Newborn Assessment

    Defined: Involves deliv-ery of an infant is compli-cated by various prob-lems

    Information Gathering

    Newborn AssessmentAPGAR 2 points 1 point 0 pointsColor pink pink body blue or pale

    blue extremities all over

    Pulse above 100 below 100 none

    Reflex irritability cough or facial grimace none(Grimace) sneeze

    Activity active some flexion limp or no(flexion) movement of limbs movement

    Respiratory effort strong cry weak cry no cry

    HistoryIf poor APGAR, may be pre-term, congenital heart problem, meconiumaspiration IRDS, transient tachypnea

    Other helpful assessmentsGestational ageWeight

    Decision Making

    If APGAR Score is:

    0 to 3 PERFORM CPR

    4 to 6 Administer oxygen, place infant in warm, neutrally thermalenvironment, generally stimulate the baby

    7 to 10 Monitor normally

    What to expectWill commonly have to do an

    APGAR score. You may have topick the 5 essential elements from

    a list. Dont be tempted by anytests other than APGAR criteria

    unless they can be done by simplylooking at the infant.

    Or, you may be given the ele-ments and asked what you want to

    do about it.

  • Meconium Aspiration

    Defined: Infant born hav-ing meconium in ventila-tion spaces

    Information Gathering

    Visual AssessmentHistory of meconium-colored amniotic fluidOften with full-term infantsInfant may have meconium staining about the bodyMay demonstrate grunting, retractions, nasal flaringPoor color (cyanosis)

    Bedside (Patient Contact) AssessmentAPGAR score between 0 and 6

    Basic Laboratory AssessmentABGshypoxemia with respiratory acidosis, metabolic acidosis or mixedChest X-rayBilateral densities and widespread atelectasis

    Special Assessments

    Decision Making

    Remove the meconium from the airway. If possible, suction the baby as soon as the headappears from the birth canal.

    Intubate to facilitate suctioning

    Reintubate if tube becomes clogged for any reason

    Mobilize secretions with chest physiotherapy.

    Mechanically ventilate only if needed

    Apply supplemental oxygen as needed.

    What to expect

    This is a very common case on thetest. It is fairly straight-forwardand easily recognized. The key tothis is repeated suctioning andclearing of the airway.

  • Sudden Infant Distress Syndrome

    Defined: Sudden apneaoccurring in newborn in-fants as a results of animmaturity central con-trol of ventilation.

    Information Gathering

    Visual AssessmentHistory of pre-term birthFamily genetic predispositionObserved, irregular respirations, bradycardia may increase risk of SIDS

    Bedside (Patient Contact) AssessmentCold air on infants face may induce apneaDiminished or absent Moro and Babinski reflexes

    Basic Laboratory Assessment

    Special Assessments

    Decision Making

    Provide oxygen when in crisis (30 and 50%)

    Do not send infant home without an apnea monitor and parental education

    If offered, teach parents CPR.

    What to expectSomewhat rare case on the test.

    Nothing particularly challenging.

  • Infant Respiratory Distress Syndrome

    Defined: Condition in in-fants where alveolus ma-turity is below normal.

    Information Gathering

    Visual AssessmentHistory may show pre-term infantOnset can be immediately after birth or within a few hoursGeneral respiratory distress, ie grunting, nasal flaring, retractionsCyanosis

    Bedside (Patient Contact) AssessmentAPGAR score between 0 and 6

    Basic Laboratory AssessmentChest-Xrayradiological description such as ground glass, honeycomb,

    reticulogranularABGspersistent hypoxemia in spite of elevated FIO2

    Special Assessments

    L/S ratio2:1 or higher is normal. Less than that shows lung immaturity

    Decision Making

    Help lung maturity through surfactant therapy with agents like Exosurf or Survanta

    2 to 5 ml/kg split among 2 to 4 dosesAdminister directly down the airwayChange infants position after every dose for 30 seconds to distribute

    the agent

    Provide oxygen via a hood. May use CPAP to oxygenate

    Mechanically ventilate with ventilatory failure, use SIMV mode on all infants. May considerreverse I:E ratio

    Note: If X-ray changes from signs of IRDS to hyperinflation and fibrosis, then the problemmay have developed into Bronchopulmonary Dysplasia. Treat as prolonged IRDS by:

    maintaining pH of 7.25 to 7.40, PaCO2 45 to 60 torr, PaO2 55 to 70 torr. Use low FIO2 Keep mean airway pressure at a minimum Wean only gradually and as tolerated, often fails initial attempts Extubate if respiratory rates are between 5 and 15 breaths

    What to expect

    This is a common case on the test.Key is remembering to addresslung maturity.

    Also, if prolonged ventilation isrequired, Bronchopulmonary Dys-plasia may develop. Be patientand treat moment to moment.

  • Congenital Heart Defects (Infant)

    Defined: Infant is bornwith an anatomical mal-ady of the heart or thevessels that emanatefrom the heart.

    Information Gathering

    Visual AssessmentHistory of pre-term birthGeneral signs of respiratory distress (grunting, nasal flaring, retractions)Cyanosis that persists in spite of high FIO2

    Bedside (Patient Contact) AssessmentHeart sounds are abnormal upon auscultation (murmur present)

    Special AssessmentsEchocardiogram is the best diagnostic test for all cardiac defects

    Decision Making

    Specific Defect Attributes

    Coarctation of the Aorta (narrowing of aorta)Hypertension in the upper extremities, hypotension in lower extremities

    Transposition of the Great VesselsAorta and pulmonary artery are switched.Aorta rising from the right heart, pulmonary artery rising from the left heart

    Patent Ductus Arteriosis (ductus arteriosis never closes)Diagnosed by comparing blood gases from the radial artery and the umbilicalartery. Positive for PDA if difference is greater than 15 torr. (PDA with a rightto left shunt)

    Other ProblemsTetralogy of Fallot

    boot-shaped heart, overriding aortaAtrial septal defect (ASD)Ventricular septal defect (VSD)Truncus arteriosis (pulmonary artery same as aortacombined vessel)

    ALL CONGENITAL DEFECTS ARE TREATED WITH SURGERY !!

    Prior to surgery simply provide supportive care such as:oxygen to keep PaO2 > 60 mm Hg.mechanical ventilation when ventilatory failure is shown by ABGs

    What to expectYour skills in recognizing com-mon congenital heart problems

    will be tested.

    Otherwise, you will be simplyproviding supportive care until

    surgery.

  • Neonatal Diaphragmatic Hernia

    Defined: Condition wherethe diaphragm nevergrows closed. Usuallyoccurs on the left side

    Information Gathering

    Visual AssessmentGeneral respiratory distress, ie grunting, nasal flaring, retractionsCyanosisBarrel chest or scaphoid abdomenMedistinal shift

    Bedside (Patient Contact) AssessmentBreath sounds absent (usually on left)

    Basic Laboratory AssessmentChest-Xrayshow intestinal parts in the chest area. Also may see a mediastinal

    shift away from the affected side.ABGsPoor

    Special Assessments

    Decision Making

    TREATMENT IS SURGERY

    Use low ventilatory pressures

    Do not use manual bag and resuscitation if possible

    May use gastric tube to decompress stomach and intestines.

    All other care is supportive

    What to expect

    This case is more about what youshould not do. Otherwise usegeneral supportive care.

  • Choanale Atresia

    Defined: Infant is bornwith an anatomical mal-ady of the heart or thevessels that emanatefrom the heart.

    Information Gathering

    Visual AssessmentNormal appearing, normal color, cyanosis during feeding

    Bedside (Patient Contact) AssessmentDuring breast or bottle feeding, baby becomes apneic and cyanoticSlight inspiratory stridor

    Special AssessmentsNeck and chest x-rays rule out airway inflammationDiagnosis by attempting to pass a suction catheter through the nares.If unable to pass, then positive

    Decision Making

    Care in feeding

    Correct with Surgery

    What to expectYour skills in recognizing com-mon congenital heart problems

    will be tested.

    Otherwise, you will be simplyproviding supportive care until

    surgery.

  • Laryngotracheobronchitis

    Defined: Otherwiseknown as Croup. Resultsfrom a viral infection thatillicits inflammation in theupper airway.

    Information Gathering

    Visual AssessmentHistory of cold in the past few daysBarking coughAge is 6 months to 3 yearsStridorTachypnea

    Bedside (Patient Contact) Assessment

    Special AssessmentsLateral Neck X-rayswelling below the glottis sometimes described as steeple

    sign or pencil point.

    Decision Making

    Priorityplacement in an oxygen tent with 30 to 40%

    Aerosolized Racemic Epinephrine

    Intubation if patient is described as lethargic, markedly diminished breath sounds, severeor marked stridor, extreme accessory muscle use

    Extubation should be done when swelling has ceased.

    What to expectYou will likely be tempted to treat

    this like Acute Epiglottitis in anemergency fashion.

    Repeated racemic epinephrinetreatments may make you feel

    uncomfortable

  • Acute Epiglottitis

    Defined: Condition wherethe epiglottis and adja-cent upper airway tissuesare infected with a bacte-ria causing inflammationand commonly threaten-ing airway patency.

    Information Gathering

    Visual AssessmentSudden onset of sickness, within 12 hours, often occurs in the eveningAge 3 to 10 yearsGeneral appearance may show drooling, hoarseness, quiet coughMay hear a softened inspiratory stridorTachypnea and tachycardia

    Bedside (Patient Contact) AssessmentPatient unable to swallow, will usually not be crying, eyes are bigSignificantly elevated body temperature, taken axillary, or tympanically

    Basic Laboratory Assessment

    Special AssessmentsLateral neck x-ray will show supraglottic inflammation

    Decision Making

    Primary and immediate concern is establishing and airway as complete closure from inflam-mation. Since inadvertent stimulation from oral intubation attempts could immediately illicitan inflammatory response, intubating in a surgical environment is very helpful. There may beneed to place a tracheostomy tube.

    Antibiotic therapy to correct bacterial infection

    Oxygen therapy at 30 to 40%

    Extubate only when inflammation is gone

    What to expect

    This case will test your immedi-ately ability to realize that it is anemergency. Stridor may temptyou to treat it more casually likecroup.

    There is a good chance you willsee Epiglottitis or Croup on thetest.

  • Bronchiolitis /RSV

    Defined: Acute vital in-fection of lower respira-tory tract usually occur-ring in infants less than18 months old. Com-monly caused by the res-piratory syncytial virus.

    Information Gathering

    Visual AssessmentGeneral signs of respiratory distress including retractions and accessory muscle

    use.Tachypnea and tachycardiaHistory of recent sickness from ages 2 months to 3 years old

    Bedside (Patient Contact) AssessmentLow grade feverWheezing, rales, and rhonchi

    Basic Laboratory AssessmentChest X-ray show scattered infiltrates and hyperlucency

    Decision Making

    Primary treatment is delivery of the drug Ribavirin which must be administered via aSPAG unit (small volume particle aerosol).

    Utilize a scavenger system, filters, and masks.

    What to expectThere is nothing particularly diffi-cult about this case. You must beprepared to recommend the use of

    a SPAG unit.

    Not commonly seen on the exam.

  • Cystic Fibrosis

    Defined: An inheriteddisorder resulting in themass production of thickmucus in the lungs.

    Information Gathering

    Visual AssessmentFamily history of disease, siblings may have it.Emaciated in appearance and body frame may be small or ageSputum production of thick voluminous purulent secretionsCan look like a young COPD patient, barrel-chested

    Bedside (Patient Contact) AssessmentDecreased flow rates such as FEV1

    Basic Laboratory AssessmentChest X-raylooks like COPD, hyperinflation, increased A-P diameter, diaphragm

    flattening

    Special AssessmentsSweat Chloride Testshow sweat chloride > 60 mEq/L

    Decision Making

    Primary treatment relates to the need to mobilize and remove secretions.

    Secretion removal promotion therapies:PEP therapy devicesChest physiotherapy with postural drainageHydration devices such as heated aerosol or ultrasonic nebulizationVibration therapy

    Oxygen as needed

    Antibiotic therapy when infection is presentoften is

    Medications used commonly include Tobramycin and Pulmozyme

    What to expect

    Not commonly seen on the exam.Tests your ability to recognizesecretion removal therapies andmay check your understandingwhen and how to modify therapy.Ex, when CPT doesnt work, usePEP therapy or ultrasonic nebuli-zation.

  • Hypothermia

    Defined: Exposure tocold such that body tem-perature falls signifi-cantly.

    Information Gathering

    Visual AssessmentHistory of exposure to cold. May be seen in homeless persons.Lethargy and unconsciousnessBradycardia, bradypnea

    Bedside (Patient Contact) AssessmentBody temperature less than 36 deg C

    Basic Laboratory Assessment

    Special Assessments

    Decision Making

    Oxygen via a heated aerosol at 40 to 100%

    Keep resuscitation efforts going until body temperature is normal.

    Mechanically ventilate as needed.

    Keep in mind that blood gas values may be altered because of the difference in blood tem-perature and analyzed temperature. Watch out of oxygen (PaO2). In cold, uncorrectedblood, PaO2 may appear higher than it actually is.

    What to expectNot very common. However

    when seen, may be seen in con-junction with other problems such

    as AIDS, or tuberculosis.

  • Burn Trauma/CO Poisoning

    Defined: Results fromdirect exposure to fireand or smoke. Directlythreatens airway andoxygen carrying capacityof the blood.

    Information Gathering

    Visual AssessmentDiagnosis is based largely on historyexposure to fire or smoke. Often occurs in

    occupational related cases (fire fighter)Visible burns about the body and faceSinged nasal and or eyebrow hairsCherry-red color of face with CO poisoningPatient is often confused or unresponsiveStridor, hoarseness

    Bedside (Patient Contact) AssessmentBreath soundswheezing, rhonchi, rales

    Basic Laboratory AssessmentABGsinitially decreased PaCO2, normal PaO2, decreased saturation. Latter may

    develop into respiratory acidosisChest X-raymay be clear at first, but later may show pulmonary edema and

    markedly decreased lung compliance

    Special AssessmentsCOHb 20% or more

    Decision Making

    Protect airway by establishing an artificial airway immediately. Particularly if there is respi-ratory distress and there are burns about the face.

    For CO poisoningstart 100% oxygen immediately even if only suspect itdo not waitfor COHb results

    Continue oxygen therapy until COHb level is below 10%.may use hyperbaric medicine ifofferedoften will not be offered.

    Practice Reverse isolation (protect the patient from staff)

    Mechanically ventilate as needed.

    What to expect

    Fairly common case on the test.Remember to focus on the airwayand on oxygen carrying capacityof the blood. Remember to em-ploy isolation techniques. Other-wise, provide general respiratorytherapy.

  • Diabetes

    Defined: Condition re-lated to failure of the re-nal system resulting inthe inability to dispose ofCO2. Respiratory resultis often respiratory keto-acidosis

    Information Gathering

    Visual AssessmentHistory of diabetesLethargy, confusion, unresponsivenessRespiratory rate and patternsignificant in depth and rate with an irregular

    rhythm (Kussmauls)

    Bedside (Patient Contact) AssessmentPedal Edema

    Basic Laboratory AssessmentABGsProfound metabolic acidosisUrine output is markedly decreased (less than 20 ml per hour)

    Special AssessmentsBlood glucose - > 160 mg (Normal 80-120 mg)

    Decision Making

    Must watch for ventilatory failure from prolonged ventilatory effort and fatigue.

    Administer electrolytes (K+, Na+, HCO3-, Cl-) as needed.

    Provide fluid as needed.

    Correct ketoacidosis.

    What to expectMay be tempted by profoundly

    acidodic pH. Only determinerespiratory failure through theCO2, or a sudden decrease in

    ventilatory volumes and breathingrate.

  • AIDS

    Defined: Disease of theimmune system com-monly resulting in pneu-mocystis carinii, a type ofpneumonia

    Information Gathering

    Visual AssessmentPrevious history of HIV positive test resultsEmaciation, unexplained weight-loss, diarrhea, low-grade fevers, night sweats,Commonly homosexual activity or drug usage is admitted

    Bedside (Patient Contact) Assessment

    Basic Laboratory Assessment

    Special AssessmentsPositive HTLV IIIELISA test positive for HIVBronchoscopyfrom lung washings or biopsy may show pneumocystis carinii

    Decision Making

    Exercise Universal Precautions

    Aerosolized Pentamadineusually done monthly

    When administering Pentamadine, use one-way valves and filters.

    What to expect

    Increasing in frequency on theexam. Sometimes is combinedwith tuberculosis, hypothermia,and others. Suspect them all.

  • LindseyJonesP u b l i s h e r s o f S c i e n c e a n d M e d i c i n e

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    Copyright 2009 LindseyJones, LLC. All Rights reserved. The enclosed material is intended to facilitate preparation for theassociated credentialing exam. The information is not intended to direct healthcare practitioners on methods of practice.