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UPPER & LOWER RESPIRATORY & PLEURAL DISEASE AHD Sept 13, 2012 DR J KOZAR CCFP(EM)

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UPPER  &  LOWER  RESPIRATORY  &  PLEURAL  DISEASE  

AHD  Sept  13,  2012  DR  J  KOZAR  CCFP(EM)  

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CASE  

•  59  yr  old  male  with  3  days  – Cough  with  yellow  sputum  – Fever,  rigors  – Right  pleuriQc  chest  pain  – SOB  on  exerQon  – Past  med  hx  

•  HTN  •  DM  II  •  Smoker  

– Exam  •  T38.2,  HR  128,  BP  146/90,  RR  24,  O2  sat  91%  room  air  •  Crackles  right  upper  chest  •  Glucoscan  15  mmoL/L  

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QuesQons  

•  Clinical  diagnosis?  – Xray?  – CT?  – Blood  cultures?  

•  DisposiQon    – Admit?  

– ICU?  •  AnQbioQcs?  

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Clinical  Diagnosis  

•  Baseline  prevalence  of  CAP  in  unselected  pts  with  suspicion  of  CAP  =  5%  

•  Review  ArQcles  (1997,  2003)  – Typical  symptoms  disQnguish  poorly  between  CAP  and  other  respiratory  illnesses  

– Clinical  signs  limited  value  in  ruling  in  or  out  CAP  •  Auscultory  findings  absent  in  25%  with  CAP  •  Significant  interobserver  variability  

– NO  evidence  to  support  use  of  History  and  Physical  exam  ALONE  to  include  or  exclude  the  diagnosis  of  CAP  

•  CXR  required  

Evidence  Based  Emergency  Medicine,  1st  ed,  p  101-­‐2.  

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CXR  

•  Long  considered  Gold  Standard  for  CAP  diagnosis  

•  Flaws  – Interobserver  variability  

• Rates  of  agreement  among  radiologists:  80%  

• EP  Overdiagnosis  – 2  studies  showed  20%  and  18.9%  of  EP  diagnosed  pneumonia  read  as  Normal  by  radiologist  

• EP  underdiagnosis  – 2  studies  showed  0.35%  and  3.1%  of  missed  posiQve  CXRs  

Evidence  Based  Emergency  Medicine,  1st  Ed,  p  102  

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CXR  

•  Comparison  of  CXR  vs  CT  – One  small  study  showed  30.8%  of  pneumonias  seen  on  CT  were  missed  on  CXR  

•  ?should  proceed  to  CT  if  high  index  of  suspicion  and    normal  or  equivocal  CXR  – ?treat  empirically  for  pneumonia  – ?repeat  CXR  in  24-­‐48  hrs  

Evidence  Based  Emergency  Medicine,  1st  Ed,  p  102  

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Should  this  paQent  be  admijed?  

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•  Joint  commijee  to  develop  unified  document  for  CAP  – CAP  &  influenza:  7th  leading  cause  of  death  in  US  – Directed  at  Primary  care,  EPs,  Hospitalists  in  US  &  Canada  

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Admission  Decision  

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Admission  Decision  

• PredicQon  rule  derived  from  database  of  >14,000  pts    • Validated  on  database  of  >  38,000  pts  and  an  observaQonal    prospecQve  cohort  of  >2000  pts  • Risk  straQfies  into  5  mortality  classes  • Its  ability  to  predict  mortality  has  been  confirmed  in  mulQple  subsequent  studies  

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PORT SCORE

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Class  I  &  II  –  outpaQent  Class  III  –  observaQon  unit  or  short  hospitalizaQon  Class  IV  &  V  –  inpaQent     IDSA/ATS  consensus  guidelines  

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Algorithm  incorporaQng  PSI  

Halm.    Management  of  CAP.    NEJM  2002:  347:  2039-­‐2045  

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PSI  criQcisms  

•  Complex  with  20  variables  •  Emphasis  on  age  

•  Neglect  of  social  aspects  • May  underesQmate  severity  of  disease  in  younger  pts  without  comorbidiQes  

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•  BriQsh  Thoracic  Society  –  “CURB-­‐65”  •  Combined  3  prospecQve  studies  from  UK,  NZ  and  Netherlands  

•  DerivaQon  cohort  718  pts  •  ValidaQon  cohort  214  pts  

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CURB  CriQcisms  

•  Fails  to  take  in  account  co-­‐morbidiQes  that  may  be  destabilized  with  even  mild  CAP  

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Comparing  PSI  &  CURB-­‐65  

•  Unclear  which  is  superior  because  no  RCTs  •  When  compared  in  same  populaQon,  PSI  classified  slightly  more  paQents  with  CAP  in  low-­‐risk  categories  – May  be  bejer  at  avoiding  unnecessary  hospitalizaQon  

•  PSI  less  pracQcal  as  uses  20  variables  •  CURB  easier  to  remember  but  not  as  extensively  studied  

•  Commijee  preferred  CURB-­‐65  – Ease  of  use  – Designed  to  measure  illness  severity  more  than  likelihood  of  mortality  

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Comparing  PSI  &  CURB-­‐65  

•  RetrospecQve  chart  review    – PSI,  CURB-­‐65  &  modified  CRB-­‐65  performed  equally  well  for  predicQng  30  d  mortality  in  paQents  >  65  yrs  old  with  CAP  

Ochoa-Gondar et al. Int J Clin Prac 2011; 65: 1165-1172.

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Caveat  

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ICU  Admission  

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 3    minor  

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ICU  admission  

•  These  are  proposed  criteria  that  need  prospecQve  validaQon  

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DiagnosQc  TesQng  

•  Clinical  features  – Cough  – Fever  – Sputum  – PleuriQc  chest  pain  

•  CXR  infiltrate  – Physical  exam  less  sensiQve  and  specific  than  CXR  – Elderly  

•  Clinical  features  and  physical  exam  findings  may  be  lacking  or  altered  

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DiagnosQc  TesQng  for  EQology  

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DiagnosQc  TesQng  for  EQology  

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Blood  Cultures  

•  Vast  majority  of  studies  have  cast  doubt  on  the  clinical  value  of  blood  cultures  – Significant  +ve  results  

• 1.4-­‐2.1%  outpts  • 5-­‐14%  inpts  • >60%  +ve  for  S.  pneumonia  

– No  systemaQc  reviews  – No  RCT  assessing  clinical  impact  of  BC’s  – Rosen’s:  “RouQne  blood  cultures  are  of  essenQally  no  value  in  nonimmunocompromised  adults”    

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Sputum  Gram  Stain  and  Culture  

•  Yield  variable  and  influenced  by  – Specimen  collecQon  

– Rapidity  of  transport  and  processing  – Skill  in  interpretaQon  – Absence  of  prior  anQbioQc  therapy  

•  Rosen’s:  “Sputum  Gram's  stain  rarely  results  in  a  change  in  therapy  or  outcome”  

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EQologic  Agents  

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EQologic  Agents  

•  ID  of  specific  pathogen  rarely  possible  within  ED  Qmeframe  – Oven  not  idenQfied  with  inpt  evaluaQon  &  Rx  – Empiric  Abx  on  basis  of  most  likely  pathogens  

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Treatment  OutpaQent  

Amoxicillin  1g  Qd  Clavulin  2g  bid  Cefuroxime  500  mg  bid  Cefpodoxime  Cevriaxone    

NB.    European  &Australasian  Guidelines  recommend  B-­‐Lactams  (usually  Amoxil)  recognizing  that:  -­‐macrolide  resistance  rising  -­‐atypicals  usually  mild  in  outpt  -­‐intermediate  resistance  S.  Pneumoniae  can  be  treated  With  B-­‐lactams  

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Treatment  OutpaQent  

•  Cochrane  Review  2009  – Currently  available  evidence  from  RCTs  is  insufficient  to  make  evidence-­‐based  recommendaQons  for  the  choice  of  anQbioQc  to  be  used  for  the  treatment  of  CAP  in  ambulatory  paQents  

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Treatment  InpaQent  

Cefotaxime  Cevriaxone  Ampicillin  Ertapenem  

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Treatment  ICU  

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Treatment  –Other  ConsideraQons  

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First  Dose  Abx  

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DuraQon  Abx’s  OutpaQent  

•  7-­‐10  days  or  longer  tradiQonal  •  Few  well-­‐controlled  studies  •  Levofloxacin  

– 750  mg  X  5d  vs  500mg  X7-­‐10d  – Equally  succcessful  and  resulted  in  more  afebrile  paQents  by  day  3  

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Bipap  

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Influenza  

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Pandemic  H1N1  Rx  Guidelines  

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(Tamiflu)

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Pneumonia  and  HIV    

•  HAART  and  PCP  prophylaxis  reduce  risk  of  opportunisQc  infecQons  – S  pneumonia  more  common  than  PCP  

• Most  common  cause  bacterial  pneumonia  •  7-­‐10  X  higher  incidence  than  non  HIV  •  Bacterial  infecQons  more  common  with  CD4  >800  

– M  tuberculosis  • More  common  with  CD4:  250-­‐500  cells/mm3  

– PneumocysQs  jirovecii(carinii)  •  CD4  <200  

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PCP  

•  Clinical  – Subacute  onset  of    

• NonproducQve  cough  • Fever  • SOB,  hypoxia  • Wt  loss  

• Tachypnea  • Tachycardia  •  Increased  LDH  (compared  with  non  PCP  pneumonia)  

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Classic  findings:  -­‐bilateral  intersQQal  Infiltrates  begin  perihilar  Other:  -­‐normal  -­‐lobar  infiltrates  -­‐pleural  effusions  -­‐hilar  adenopathy  -­‐parenchymal  nodules  -­‐cavitary  disease  -­‐pneumothoraces  

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HIV  pneumonia  

•  Treatment  – Cover  for  PneumocysQs  and  bacterial  pathogens  

• TMP-­‐SMX,  20mg/kg  TMP  divided  qid  X  21d  • Prednisone  for  PaO2<70  mmHg  

– 40mg  bid  

– Consider  TB  in  all  HIV+  • Resp  isolaQon  unQl  ruled  out  

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TB  

•  About  1/3  of  world’s  populaQon  infected  – Worldwide  8  million  develop  acQve  TB,  2  million  die  per  year  

•  AcQve  TB  develops  – Within  2  yrs  of  infecQon  in  5%  – Another  5%  reacQvaQon  disease  later  

•  Risk  increased  with  impaired  cell  mediated  immunity  – DM,  CRF,  malnutriQon,  immunosuppressive  Rx  – HIV+  with  +skin  test  

» 8%  risk/yr  – MulQdrug  resistance  increasing  

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•  Clinical  – Cough,  non  producQve  or  producQve  – Fever  avernoon,  night  sweats  – Wt  loss,  faQgue,  malaise,  headache  – Hemoptyis  about  30%  

•  Non  specific  so  index  of  suspicion  dependent  on  symptoms,  risk  factors  

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•  Risk  factors  – Close  contacts  with  known  case  – HIV+  – From  Asia,  Africa,  LaQn  america  – Medically  underserviced,  homeless  – Elderly  – LTC  residents  – IVDU  – OccupaQonal  exposure  

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xray  

•  Classic:  upper  lobe  infiltrate  or  consolidaQon  +/-­‐cavitary  lesions  

•  Normal  CXR  has  high  NPV  for  acQve  TB  – 1%  false  neg  in  immunocompetent  

– Up  to  40%  false  neg  in  HIV+  for  acQve  TB  

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Low  Risk  Criteria  for  TB  

•  Non-­‐immigrant  •  No  weight  loss  •  No  posiQve  Mantoux  or  Hx  TB  

•  Not  homeless  

•  Not  recently  incarcerated  •  CXR:  No  cavitary  or  apical  infiltrate  •  Absence  of  all  above-­‐  NPV  of  99.7%  

– CI  (99.1-­‐99.9%)  

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ReacQvaQon  TB    (Post-­‐Primary)  

CavitaQng  lesion  RLL  

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Primary  TB  

•  Primary  TB  – Pneumonic  infiltrate  any  lobe  

•  Like  any  bacterial  pneumonia  

– Enlarged  hilar  or  mediasQnal  nodes  

– Pleural  effusion  – Miliary  TB  

Primary  TB  in  young  child  

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Primary  TB  

Extensive  right  paratracheal  adenopathy  and  poorly  defined  rul  consolidaQon  in  primary  TB  

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TB  suspected?  

•  Respiratory  isolaQon  – Surgical  mask  on  paQent  – NegaQve  airflow  room  – Coughing,  sneezing,  talking  produce  infecQous  droplets  which  dry  rapidly  

– InfecQve  parQcle  circulate  airborne  for  prolonged  periods  • 1-­‐5  um  and  travel  to  distal  alveoli  • N95  masks  

•  Respirology  Consult  

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Case  

•  87  yr  old  female  from  LTC  – Choked  while  eaQng  breakfast  this  morning  

– Cough  for  several  hours  but  seems  to  be  improving  

– RR  20,  O2  sat  93%,    T  37.5,  BP  145/85  – Chest  mild  wheezing  – PMHx  

• Stroke,  demenQa  

– ?AnQbioQcs  

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AspiraQon  PneumoniQs  

•  Inflammatory  chemical  injury  of  the  tracheobronchial  tree  and  pulmonary  parenchyma  caused  by  inhalaQon  of  regurgitated  sterile  gastric  contents  

•  Risk  Factors  – Impaired  swallowing,  protecQve  airway  reflexes  – Decreased    LOC  – CriQcally  ill  

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AspiraQon  PneumoniQs  

•  Pathophysiology  – Dependent  on  volume  and  pH  of  aspirate  – Direct  causQc  effect  –  Inflammatory  response  that  peaks  in  4-­‐6hrs  

•  Clinical    – NonproducQve  cough  – Tachypnea  – Fever    – PleuriQc  CP  – Bronchospasm  – Respiratory  distress  or  failure  – Xray  infiltrates  

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AspiraQon  PneumoniQs  

•  Treatment  – SucQon  upper  airway  – Consider  ET  tube  placement  and  sucQoning  – Bronchodilators  for  bronchospasm  – NO  AnQbioQcs  

• Not  beneficial  and  may  select  for  resistant  organisms  

– NO  steroids  • MAY  lead  to  AspiraQon  Pneumonia  due  to  breakdown  of  pulmonary  defenses  

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AspiraQon  Pneumonia  

•  Alveolar  space  infecQon  resulQng  from  the  inhalaQon  of  pathogenic  material  from  the    oropharynx  

•  Risk  Factors:  – Oropharyneal  colonizaQon  with  pathogenic  bacteria  – Impaired  swallowing  or  gag  reflex  – Elderly/LTC  residents  – May  have  clinically  obvious  episodes  of  aspiraQon  or  silent  aspiraQon  

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AspiraQon  Pneumonia  

•  Microbiology  – Strep  pneumoniae  – Staph  aureus  – Haemophilus  influenza  – Enterobacteriaceae  – Hospital  acquired  

•  Pseudomonas  •  Gram  negaQve    

– anaerobes  – Peptostreptococcus,  Bacteroides,  Fusobacterium,  and  Prevotella  spp  

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AspiraQon  Pneumonia  

Loca%on  Recumbent  paQents  

•  Posterior  segments  of  upper  lobes  

•  Superior  segments  of  lower  lobes  

Upright  paQents  •  Basal  segments  of  lower  lobes  

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AspiraQon  Pneumonia  

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AspiraQon  Pneumonia  

•  Delayed  onset  24-­‐48hrs  aver  aspiraQon  • Fever  • ProducQve  cough  • Dyspnea  •  Ill  appearance,  change  in  mental  status  

•  Increased  HR,  RR  • Lethargy  ,nausea,  vomiQng  

• Expanding  infiltrate  on  CXR  

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AspiraQon    

• Who  to  treat  with  anQbioQcs?  – Previously  healthy  adults  whose  symptoms  of  aspiraQon  pneumoniQs  fail  to  resolve  in  24-­‐48  hrs  

– Signs  of  bacterial  aspiraQon  pneumonia  

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AspiraQon  

•  Chronically  ill,  LTC  resident  with  episode  of  aspiraQon  

• Stable  and  symptoms  resolve:    – Observe  ?12-­‐24hrs  &  discharge  back  to  LTC  

• SymptomaQc  :  conQnued  observaQon,  ?admission  – PneumoniQs  <  48  hrs  

– AnQbioQcs  discouraged  because  of  lack  of  evidence  of  benefit  and  concern  about  selecQng  for    resistant  organisms  

• Worsening  symptoms:  anQbioQcs  +/-­‐  admission  

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Acute  Respiratory  Distress  Syndrome  

•  ARDS  – NonCardiogenic  pulmonary  edema  

– Nonspecific  response  of  lung  to  variety  of  insults  – DefiniQon  

• Acute  onset  • Bilateral  infiltrates  on  CXR  • PaO2/FiO2  <  200  • PAWP  <18  mmHg  (ie  No  cardiogenic  pulmonary  edema)  

• >  1  predisposing  condiQon  

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Rosen’s 7th ed

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ARDS  

•  Pathophysiology  – Results  from  damage  to  region  of  alveolar-­‐capillary  gas  exchange  

– Increased  permeability  to  plasma  fluid  and  protein  

– Mediated  by  proteases,  oxygen  radicals,  interleukins,  cytokines,  TNF,  complement  factors  

– Usually  develops  in  pts  who  are  already  seriously  ill  in  hospital  

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ARDS  CXR  

Bilateral, diffuse, patchy or homogeneous infiltrates

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ARDS  Treatment  

•  SupporQve  primarily  – High  inspiratory  pressures  and  PEEP  required  to  maintain  oxygenaQon  hence  risk  of  barotrauma  

•  Reduced  Qdal  volumes  (6ml/kg),  permissive  hypercapnia  •  Avoid  oxygen  toxicity-­‐  sats  85-­‐90%,  FiO2  <65  •  Inverse  raQo  venQlaQon  with  prolonged  inspiratory  Qme  

•  hi-­‐frequency  oscillator  venQlaQon  •  Prone  posiQoning  •  Inhaled  nitric  oxide,  NAC,  Prostaglandin  E,  Ketoconazole,  NSAIDS,  corQcosteroids  

– NO  evidence  of  benefit  

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Case  

•  33  yr  old  male  with  2  weeks  – Cough,  mildly  producQve  

– Feverish  iniQally,  resolved  – Can’t  sleep  at  night  because  of  cough  – Very  mildly  SOB  

– HR  78,  BP  135/75,  RR  16,  O2  sat  98%  – Chest:  clear  – Wants  anQbioQcs  

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Acute  BronchiQs  

•  Acute  respiratory  infecQon  – Cough  +/-­‐  sputum  

– Other  URTI  symptoms  – Not  caused  by  pneumonia  or  chronic  bronchiQs  – Usually  1-­‐3  weeks  but  can  be  longer    

• 20%  up  to  2  months  

– Typically  late  fall  to  early  spring  

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– Self  limited  inflammaQon  of  large  airways  secondary  to  infecQon  of  bronchial  epithelium  • May  involve  small  airways  too  

– Transient  bronchial  hyperresponsiveness  appears  to  be  mechanism  for  cough  

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Acute  BronchiQs  

•  Clinical  Diagnosis  – Cough  <  2weeks  – No  prior  lung  disease  – No  findings  to  suggest  pneumonia  

• T>  38C  • HR>100  • RR>24  • Focal  chest  pain  • Ausculatory  abnormaliQes  

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Acute  BronchiQs  DiagnosQc  TesQng  

•  CXR    NOT  required  in  previously  healthy,  non-­‐elderly  

• Unless  cough>  3weeks  • Evidence  of  pneumonia  

•  Spirometry  •  If  wheezing  heard  or  pt  describes  • 40%  have  reduced  FEV1  

•  Sputum  C&S  –  NO  •  Pro-­‐Calcitonin  to  r/o  bacterial  cause  ??  

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Acute  BronchiQs  Microbiology  

•  Resp  Viruses  Majority  –  Influenza  A  –  Influenza  B  – Parainfluenza  – RSV  –  Coronavirus  –  Adenovirus  –  Rhinovirus  –  coxsackievirus  

•  Atypicals  5-­‐25%  – Bordetella  Pertussis  – Mycoplasma  pneumonia  

– Chlamydia  pneumonia  – Legionella  

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Acute  BronchiQs  Treatment    

•  AnQbioQcs  – Cochrane  Review,  Dec  2007  

• Modest  beneficial  effect  – Cough  decreased  

» RR  0.64    (CI  0.49-­‐0.85)  » NNT  6  

– Night  Cough  » RR  0.67  (CI    0.54-­‐  0.83)  » NNT  7  

– ReducQon  days  feeling  ill  » 0.64  days(CI  0.13-­‐1.16)  

– ReducQon  days  with  limited  acQvity  »   0.49  days  (CI  0.04-­‐0.94)  

•  Data  on  subsets  who  benefit  lacking  

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Acute  BronchiQs  Treatment    

•  Need  to  consider  – Side  effects  – MedicalizaQon  of  self-­‐limiQng  condiQon  – Increased  anQbioQc  resistance  – $  

•  Not  recommended  because  although  staQsQcal  significance,  not  clinically  significant  – 0.6  day  reducQon  in  cough  

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Acute  BronchiQs  Treatment    

•  Bronchodilators  – Cochrane  reviews,  updated  2005  

• Limited  evidence:  2  trials  in  adults  with  inhaled  beta  2  agonists  showing  mixed  results  

• May  reduce  symptoms,  including  cough  in  paQents  with  evidence  of  airflow  obstrucQon  

– Not  well  supported  by  data  

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Acute  BronchiQs  Treatment    

•  Inhaled  Steroids  – Brief  (7day)  trial  of  inhaled  or  oral  corQcosteroids  may  be  reasonable  for  troublesome  cough  (>  20  days)  • No  clinical  data  to  support  this  

Wenzel  et  al.    Acute  BronchiQs.    NEJM  2006,  355;  2125-­‐30  

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Acute  BronchiQs  Treatment    

•  Cough  Suppressants  – Cochrane  reviews,  2007  

• No  good  evidence  for  or  against  OTC  cough  meds  in  URTI  

•  Insufficient  evidence  to  draw  any  conclusions  on  OTC  cough  meds  as  adjuncQve  treatment  for  pneumonia  

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Case  

•  25  yr  old  male  •  Onset  right  pleuriQc  chest  pain  and  SOB  yesterday  while  having  shower  

•  RR  18,  HR  94,  BP  110/65,  O2  Sat  95%  

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Case  pneumothorax  

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Pneumothorax  size  

hjp://www.chestx-­‐ray.com/calculator/PTX.html  

Light  Index  Collin’s  Method  

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Pneumothorax  Size  

American  Guidelines  

•  Small  pneumo  –  <  3cm  apex  of  lung  to  cupola  

•  Large  pneumo  –  >  3cm  

Bri%sh  Guidelines  

•  Small  pneumo  –  <2  cm  rim  visible  between  

lung  margin  and  chest  wall  •  2cm  =  49%  pneumo  

•  Large  pneumo  –  >  2  cm  

CalculaQon  methods  cumbersome  and  usually  used  for  research    purposes,  not  clinically  

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Types  of  Pneumothoraces  

Pneumothorax

Spontaneous Pneumothorax

Traumatic Pneumothorax

Iatrogenic Pneumothorax

Primary Spontaneous

Pneumothorax

Secondary Spontaneous

Pneumothorax

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Types  of  Pneumothoraces  

•  Secondary  Spontaneous  Pneumothorax    – No  precipitaQng  external  factor  – But  do  have  underlying  lung  disease  

•  COPD  –  70%  •  Asthma  •  Malignancy  

•  PCP  pneumonia  

•  CysQc  Fibrosis  – Typically  >  40  yrs  old  – Oven  more  symptomaQc  than  primary  SP’s  because  of  poor  pulmonary  reserve  

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Types  of  Pneumothoraces  

•  Primary  Spontaneous  Pneumothorax  –  Individuals  with  no  clinically  apparent  lung  disease  – But  90%  have  subpleural  bulla  (bleb)  on  CT,  typically  at  apex:  emphysema-­‐like  changes  

–  Incidence  (1)  •  15/100,000/year  in  men  •  5/100,000/year  in  women  

– Mortality  •  0.09%  men  •  0.06%  women  

1.  Rosen’s  Emergency  Medicine  6th  Ed,  2006;  1143  -­‐1145.  

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Types  of  Pneumothoraces  

– Risk  factors  for  Primary  SP’s  •  Male  

•  Tall  •  Smoking  

•  Familial  

•  Mitral  valve  prolapse  

•  Marfan’s  

•  Not  related  to  physical  exerQon  – Typical  paQent  –  healthy  male,  20-­‐40  yrs.  old,  of  taller  than  average  height,  smoker  

– Risk  of  recurrence  aver  first  SP  =  1/3    (1)  

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Treatment  Strategies  

•  ObservaQonal  studies  demonstrate  extensive  pracQce  variaQon  (2)  

•  American  College  of  Chest  Physicians  (ACCP)  commissioned  development  of  pracQce  guidelines  in  2001  (3)  – Commijee  consisted  of  32  members,  12  of  which  were  thoracic  surgeons,  4  EP’s  

– Recognized  there  is  insufficient  data  from  RCT’s  to  develop  evidence-­‐based  document  

– ACCP  recommendaQons  would  largely  derive  from  expert  opinion  

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Treatment  Strategies  

– BriQsh  Thoracic  Society  (BTS)  developed  guidelines  (2003)  by  commijee    •  substanQally  different  from  ACCP  (4)  

2.  Baumann  MH,  Strange  C.  The  clinician’s  perspecQve  on  pneumothorax  management.  Chest  1997;  112;  822-­‐828.  3.  Baumann  MH  et  al.  Management  of  Spontaneous  Pneumothorax:  An  American  College  of  Chest  Physicians  Delphi  Consensus  Statement.  Chest  2001;  119;  590-­‐602.  4.  Henry  M  et  al.    BTS  guidelines  for  the  management  of  spontaneous  pneumothorax.    Thorax  2003:  58  (Suppl  II);  ii39-­‐52.  

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Treatment  Strategies  

•  Observe  •  AspiraQon  •  Small  bore  chest  drainage  

– pigtail  •  Large  bore  chest  drainage  

– Chest  tube  •  InpaQent  vs  OutpaQent  

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Secondary  Spontaneous  Pneumothorax  

•  Admit  all  •  Small,  stable  

– Observe  or  tube  thoracostomy  or  aspirate  (BTS)  

•  Large  or  symptomaQc  – Tube  thoracostomy    

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Primary  Spontaneous  Pneumothorax  Treatment  Strategy:  

ObservaQon  •  Pleural  air  is  reabsorbed  at  about  1.25%-­‐2%  of  involved  hemithorax/day  –  If  paQent  suffers  a  25%  pneumothorax,  will  take  13-­‐20  days  to  resolve  (with  no  further  leak)  

– Supplemental  O2    will  increase  resoluQon  rate  by  3-­‐4  fold  

•  ACCP:  Clinically  stable  paQents  with  small  pneumothorax  (<3cm  apex  to  cupola)  can  be  discharged  home  aver  3-­‐6  hrs  of  observaQon  and  a  repeat  CXR  which  excludes  progression,  with  follow-­‐up  in  12hrs  to  2  days  

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Treatment  Strategy:  ObservaQon  

•  BTS:  paQents  with  small  (<2cm  lung  to  chest  wall)  SP  and  without  SOB  can  be  discharged  with  early  follow-­‐up  –  no  recommendaQon  for  observaQon  in  ED,  repeat  CXR  

•  CriQcisms:  –  Some  SP’s  are  trivial  in  size  but  cause  a  lot  of  symptoms  which  only  

resolve  with  evacuaQon  of  air  –  Very  small  risk  of  tension  pneumothorax  –  Some  observed  paQents  eventually  need  tube  drainage  because  of  

ongoing  leak  (5)  

5.    Baumann  MH  and  Strange  C.  Treatment  of  spontaneous  pneumothorax:  a  more  aggressive  approach?  Chest  1997;  112;  789-­‐804.  

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•  ACCP:  recommend  for  stable  paQents  with  large  SP  (>3cm  apex  to  cupola)  should  have  small  bore  catheter  (<14F)  eg.  pigtail  catheter  or  16F-­‐22F  chest  tube  and  be  hospitalized  – “Reliable  paQents  who  are  unwilling  to  undergo  hospitalizaQon  may  be  discharged  home  from  ED  with  small  bore  catheter  ajached  to  Heimlich  valve  if  the  lung  has  reexpanded  aver  the  removal  of  pleural  air.      

     Follow-­‐up  should  be  arranged  within  2  days    (good  consensus)”    

Primary  Spontaneous  Pneumothorax  Treatment  Strategy  

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Primary  Spontaneous  Pneumothorax  Treatment  Strategy  

•  BTS:  For  paQents  with  SOB  and/or  large  SP  (>2cm  air  lung  to  chest  wall)  recommend  small  chest  tube  (10-­‐14F)  only  if  aspiraQon  and  reaspiraQon  unsuccessful  

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Treatment  Strategy:  AspiraQon  

•  ACCP:  AspiraQon  not  recommended  – “rarely  appropriate  in  any  clinical  circumstance”  

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Treatment  Strategy:  AspiraQon  

•  ProspecQve,  randomized,  pilot  study  of  aspiraQon  (16G  IV  needle)    vs.  chest  tube  in  primary  SP  (6)  

–  16/27  (59.3%)  immediate  success  with  aspiraQon,  repeat  aspiraQon  in  6/11  but  0%  successful.  

•  9/11  had  chest  tubes-­‐  all  successful  •  2/11  had  immediate  thoracoscopy  •  Report  a  1  week  intenQon  to  treat  success  rate  of  25/27  (93%)  of  aspiraQon  plus  

chest  tube  –  21/33  (63.6%)  ”immediate  success”  with  chest  tube  (16-­‐20F)  which  meant  

tube  out  by  72  hrs  •  1  week  success  rate  28/33  (85%)  

–  “StaQsQcal  power  insufficient  to  confirm  therapeuQc  equality”  

6.  Noppen  M  et  al.  Manual  AspiraQon  versus  Chest  Tube  Drainage  in  First  Episodes  of  Primary  Spontaneous  Pneumothorax.  Am  J  Respir  Crit  Care  Med  2002;  165;  1240-­‐1244.  

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Treatment  Strategy:  AspiraQon  

•  RetrospecQve  analysis  from  Hong  Kong  of  91  consecuQve  primary  SP’s  who  underwent  aspiraQon  (16G  cannula)  – Overall  success  rate  50.5%  (7)  

• Pneumo  >  40%   15.4%  success  • Pneumo  21-­‐39%   61.8%  success  • Pneumo  <20%     68%  success  

7.  Chan  S,  Lam  P.  Simple  aspiraQons  as  iniQal  treatment  for          primary  spontaneous  pneumothorax:  results  of  91    consecuQve  cases.    J  Emerg  Med.  2005;  28;  133-­‐138.  

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Treatment  Strategy:  AspiraQon  

•  RetrospecQve  review  of  SP  (primary  and  secondary)  in  Singapore  (8)  

–  N=159  –  75  (47.2%)  treated  with  chest  tube  (?size)  with  complete  reexpansion  

in  65.3%  –  28  (17.6%)  had  needle  aspiraQon    

•  complete  reexpansion  in  only  5/28  (17.9%)  •  50%  requiring  either  reaspiraQon  or  subsequent  chest  tube  (42.9%)  •  all  were  admijed  for  monitoring  

–  56  (35.2%)  were  admijed  and  observed  

8.  Ong  M  et  al.  Spontaneous  Pneumothorax  Outcome  Study:  a  2  year  review.    European  J  of  Emergency  Medicine  2004;  11;  89-­‐94.  

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Treatment  Strategy:  AspiraQon  

•  SystemaQc  review  in  2004  looked  at  3  RCTs  comparing  simple  aspiraQon  and  chest  tube  12  –  Evidence  limited;  sample  size  too  small  to  make  any  firm  conclusion  –  Couldn’t  combine  success  rates  because  of  differences  in  outcome  

definiQons  –  Couldn’t  pool  pain  scores  –  AspiraQon  resulted  in  shorter  hospitalizaQon,  but  hospitalizaQon  

mandated  with  chest  tube  –  Doesn’t  address  use  of  small  bore  (8-­‐14F)  catheters  or  outpaQent  

treatment  

12.  Devanand  et  al.    Simple  aspiraQon  versus  chest-­‐tube  inserQon  in  the  management  of  PSP:  a  systemaQc  review.      Respiratory  Medicine  2004;  98;  579-­‐590.  

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Treatment  Strategy:  AspiraQon  

•  2006  RCT  from  Kuwait  of  aspiraQon  vs  chest  tube  drainage  in  PSP  (N=137)  13  –  AspiraQon    

•  immediate  success  40/65  (62%)  •  1  week  success  58/65  (89%)  intenQon  to  treat  •  3  month  recurrence    15%  •  ComplicaQons  1  (2%)  

–  Chest  tube  (20F)  •   immediate  success  49/72  (68%)  •  1  week  success  63/72  (88%)  •  3  month  recurrence  8%:  not  significant  •  ComplicaQons  5  (7%)  

13.  Ayed  et  al.  AspiraQon  versus  tube  drainage  in  PSP:  a  randomized  study.    European  Respiratory  Journal  2006;  27;  477-­‐482.  

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CriQcal  appraisal  

•  3  RCT’s,  fair  quality  •  No  significant  difference  between  needle  aspiraQon  and  tube  thoracostomy  –  Immediate  failure,  1  week  failure  – ComplicaQons  – 1  yr  recurrence  

•  Needle  aspiraQon  – Lower  rates  of  hospitalizaQon  and  length  of  stay  

•  Conclusion  – Needle  aspiraQon  at  least  as  safe  and  effecQve  – Benefit  of  fewer  hospital  admissions  and  shorter  stay  

Zehtabchi  ,  Rios.    Management  of  Emergency  Department  PaQents  with  Primary  Spontaneous  Pneumothorax:  Needle  AspiraQon  or  Tube  Thoracostomy?    Annals  of  Emerg  Med  2008:  51:  91-­‐100  

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Consensus?  

•  Small    (<3cm  apex  to  cupola)  and  AsymptomaQc  first  episode  of  PSP  should  be  observed  for  several  hours  and  discharged  if  stable  

•  A  large  (>  3cm)  or  symptomaQc  first  PSP  should  be  treated  with  air  evacuaQon:  – Small  catheter  manual  aspiraQon-­‐once  only  OR  – Small  (14F)  percutaneous  catheter  with  Heimlich  valve-­‐  outpaQent    OR    water  seal  device  –inpaQent  14  

14.  Baumann  and  Noppen.  Pneumothorax.  Respirology  2004.  9;  157-­‐164  

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Consensus?  

•  Blurring  of  disQncQon  between  aspiraQon  and  chest  catheter  is  making  the  debate  moot:  15,16  –  BTS  guidelines  also  advocated  in  centres  with  experQse  the  use  of  

small  bore  catheter  aspiraQon  kits  (8F  seldinger)  lev  in  place  unQl  re-­‐expansion  confirmed  

–  IV  cannula  (16  gauge)  in  inexperienced  hands:  •  Frequently  kinks  •  Difficult  to  keep  sealed  and  in  place  while  a  f/u  CXR  is  done  •  Doesn’t  effecQvely  exclude  a  persistent  air  leak  •  40-­‐50%  require  a  second  procedure  ie  tube  thoracostomy  

–  If  small  bore  catheter  used  as  iniQal  strategies,  comes  down  to  Qming  of  removal  and  choice  of  catheter  

15.  Baumann.  Management  of  SP.  Clinics  in  Chest  Medicine  2006;  27;  369-­‐381  16.    Henry.  Simple  sequenQal  treatment  for  PSP:  one  step  closer.    European  Respiratory  Journal  2006;  27;  448-­‐450.  

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Consensus?  

•  Pilot  study  2006:  “One  system,  Serial-­‐steps  approach”  to  PSP  17  – 41  paQents,  8.5F  pigtail  catheter  via  seldinger,  anterior  route,  connected  to  Heimlich  and  all  admijed  

•  24  hr  success  rate  61%  (tube  out  and  home)  •  1  week  success  rate  85%  •  Analgesic  use  

–  8/41  required  none  –  2/41  required  narcoQcs  during  sucQon,  –  Rest  needed  only  non-­‐narcoQc  analgesics  

•  Next  step:  outpaQent  management  algorithm  

17.  Marqueje  et  al.  Simplified  stepwise  management  of  PSP:  a  pilot  study.    European  Respiratory  Journal;  27;  470-­‐476.  

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Treatment  Strategy:  OutpaQent  Management    

•  Present  TOH  management  is  shiving  from  admission  of  paQents  with  SP  treated  with  14F  pigtail  catheter  to  selected  outpt  care  

•  OutpaQent  management  has  been  described  several  Qmes  in  the  literature  daQng  back  to  mid  70’s  in  the  thoracic  surgery  literature  

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Treatment  ComplicaQons  

•  Failure  to  expand  •  Tension  pneumothorax  •  Persistent  air  leak  •  InfecQon  •  Neurovascular  bundle  injury  •  Re-­‐Expansion  pulmonary  edema  

– Younger  (20-­‐39)  – Larger  pneumothorax  – Present  >72  hrs  &  rapidly  re-­‐expanded  with  sucQon  – Rx  is  supporQve  

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Post  Pneumothorax  

•  No  flying  unQl  resolved  •  No  scuba  –ever  •  Discourage  smoking  

•  DefiniQve  treatment  advised  aver  second  recurrence  – VATS:  Video  assisted  thoracoscopic  surgery  

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What’s  this?  

Beware  of    COPD  pts:      -­‐Paucity  of  lung  markings  make  pneumothorax  difficult  to  detect  -­‐Giant  bullae  may  simulate  pneumothorax  

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Tension  Pneumothorax  

•  Clinical  diagnosis  – Tachycardia  (HR>120)  – Hypoxia  – JVD  

• May  be  difficult  to  detect  

– Hypotension  •  Late  &  ominous  

– Tracheal  displacement  •  Rare  &  preterminal  

– Treatment?  

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Case  

•  75  yr  old  woman  with  3  weeks  of  – Progressive  SOB  on  exerQon  – Orthopnea  – Mild  cough,  non  producQve  – No  fever  – No  Chest  pain  

•  HR  85,  RR  20,  O2  sat  93%,  BP  165/95  •  Decreased  breath  sounds  right  with  a  few  crackles  

•  How  would  you  manage  with  the  following  CXR?  

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CXR  #  1   CXR  #  2  

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Pleural  Effusions  

•  Pleural  fluid  – Secreted  by  parietal  pleura  (systemic  capillaries)  

– Absorbed  by  visceral  pleura  (pulmonary  capillaries)  

– Increased  producQon  or  decreased  absorpQon  will  result  in  accumulaQon  

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Pleural  Effusions  Types  

•  Exudates  – Results  from  pleural  disease  

–   InflammaQon,  neoplasia  results  in  acQve  fluid  secreQon  or  leakage  

– High  protein  content  

•  Transudates  – Results  from  imbalance  in  hydrostaQc  or  oncoQc  pressure  

– Ultrafiltrate  with  low  protein  content  

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Pleural  Effusions  Examples  

•  Exudates  –  Cancer  –  Bacterial  pneumonia  with  

parapneumonic  effusion  –  Viral,fungal,  mycobacterial  

or  parasiQc  infecQon  –  PE  –  Rheumatologic  condiQons  – Uremia  –  PancreaQQs  –  Post  cardiac  surgery  or  

radiaQon  

•  Transudates  –  CHF  (90%)  –  Cirrhosis  with  ascites  –  Peritoneal  dialysis  – NephroQc  syndrome  –  PE  

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Light’s  Criteria  

The  fluid  is  considered  an  exudate  if  any  of  the  following  apply:    

Pleural  fluid  protein  :  serum  protein  >  0.5    

Pleural  fluid  LDH    :  serum  LDH    >  0.6    

Pleural  fluid  LDH  >    2/3  of  the  upper  limit  of  normal  serum  LDH  

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Pleural  Effusions  Clinical  Features  

•  AsymptomaQc  •  SOB  •  PleuriQc  chest  pain  

– Pleurisy=  inflammaQon  of  pleura  • With  or  without  significant  exudaQon  of  fluid  • Viral  pleuriQs  usually  preceded  by  viral  prodrome  

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Pleural  Effusions  

•  CXR  –  250-­‐500  ml  fluid  required  to  

visualize  on  PA  or  AP  CXR  

–  Lesser  amount  visible  on  lateral  view  

Ultrasound  

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Pleural  Effusions  

•  PE  is  most  commonly  overlooked  disorder  in  workup  of  pleural  effusions  

•  PE  is  most  common  cause  of  pleuriQc  CP  and  pleural  effusion  in  pt<40  

Rosen’s  6th  ediQon,  p  1151  

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Pleural  Effusions  Management  

•  ED  management  – Underlying  disease  process    

• Eg.  If  CHF    (most  common  cause)  suspected  – Diurese  first  – Thoracentesis  if    

» not  resolving  » grossly  unequal  in  size    

– Analgesia  for  pleuriQs  • NSAIDs  • opioids  

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Pleural  Effusions  Management  

•  RelaQvely  asymptomaQc  effusions  of  clear  eQology  may  not  require  any  further  ajenQon  

•  Generally,  unexplained  effusions  require  invesQgaQon  

•  Thoracentesis  – DiagnosQc  or  therapeuQc  – Usually  not  done  in  ED,  unless  paQent  unstable  

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Pleural  Effusions  Management  

•  DiagnosQc  Thoracentesis  – For  analysis  in  cases  without  a  clear  diagnosis  

• Classify  as  transudaQve  vs  exudaQve  – TransudaQve=treat  underlying  process  – ExudaQve=more  extensive  diagnosQc  workup  

» Check  pleural  fluid  pH  » pH  <  7.0  suggests  empyema  » pH  <  7.3  suggests  parapneumonic  effusion,  malignancy,  TB,  rheumatoid  effusion,    

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Pleural  Effusions  Management  

•  DiagnosQc  Thoracentesis  • Detect  pleural  space  infecQon    

– PaQents  with  pneumonia  and  significant  pleural  effusion  (parapneumonic  effusion)  

» >5cm  on  lateral  upright  CXR    (2007  guidelines)  

– Gram  stain,  C&S,  pH,  cell  count  – If  empyema,  tube  thoracostomy  required  

» Empyema  =  pus  +  bacteria  on  gram  staining  

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Pleural  Effusions  Management  

•  TherapeuQc  Thoracentesis  – For  dyspnea  at  rest  with  large  amounts  of  fluid  

– Empyema  

•  At  TOH,  mandated  to  be  done  with  US  guidance  

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Case  

•  69  yr  old  male  – Cough  for  3  weeks  – 2  days  of  coughing  up  bright  red  blood,  filling  about  5  kleenexes  a  day  

– No  chest  pain,  fever,  SOB  – Smoker  

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What’s  your  approach  to  this  paQent?  

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Hemoptysis  

•  Numerous  causes  •  Lung  has  dual  lung  supply  

– Bronchial  • Systemic  circulatory  pressure  • Supply  supporQng  structures  of  lung  

– Pulmonary  • Low  pressure  • Supply  alveoli  

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Hemoptysis  Clinical  

•  Categorized  – Mild:     <  20  ml  in  24  hrs  – Moderate:   20-­‐600  ml  in  24  hrs  – Severe:     >600  ml  in  24  hrs  – Not  helpful  in  ED  

•  ED  CategorizaQon  – Scant/blood  streaked  sputum  – Frank  hemoptysis  – Massive  hemoptysis  interfering  with  respiraQon  

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Hemoptysis  Clinical  

•  Hx  and  Px  only  moderate  roles  in  idenQfying  source  

•  Try  to  r/o  nasopharyngeal  or  GI  source  •  Associated  symptoms  may  help  

– Cough,  sputum,  fever,  dyspnea,  chest  pain,  night  sweats,  wt  loss  

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Hemoptysis  InvesQgaQons  

•  CXR    – 15-­‐30%  normal  

• Most  nonspecific  bronchiQs  

– 80-­‐90%  with  neoplasm  will  have  abnormal  CXR  

•  Other  invesQgaQons  – CT  – Bronchoscopy  

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Case    

•  45  yo  F  •  3  day  history  of  sore  throat  and  associated  fever  •  Today,  significantly  worse  +++  pain  •  Hoarse  voice  •  Can’t  eat  or  drink  •  Not  SOB  •  OE:      

–  Looks  unwell,  voice  muffled  –  T  40°C,  P100,  BP  120/60,  SaO2  95%  RA  – Oral  cavity/oropharynx:    mild  erythema  – Neck:  normal  ROM,  No  lymphadenopathy  –  Resp:    good  BS,  no  stridor,  no  tracheal  tug  

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Supraglo�Qs  

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Supraglo�Qs  

•  Epiglo�Qs:    InflammaQon  of  the  epiglo�s  •  Supraglo�Qs:    InflammaQon  of  supraglo�s  (whole  or  part)  

–  Epiglo�s  –  Aryepiglo�c  folds  –  Arytenoids  –  False  Cords  –  Pharyngeal  walls  

•  EQology:  –  InfecQon  –  Trauma  (mechanical,  thermal,  causQc  ingesQon)  

•  TradiQonally  considered  a  pediatric  condiQon  caused  by  Haemophilus  influenza  B  but  now  more  likely  to  be  seen  in  adults  

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H.  Influenza  Vaccine  

•  Hib  vaccine  – IntroducQon  has  resulted  in  a  dramaQc  decrease  in  the  incidence  of  invasive  H.  influenza  infecQons  (meningiQs,  epiglo�Qs)  

•  Health  Canada  ImmunizaQon  Monitoring  Program,  AcQve  (IMPACT)  documented  99%  fewer  invasive  Hib  infecQons  in  2000  vs  1985  (1)  

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Epidemiology  

•  Mayo-­‐Smith  et  al(2):  

–  18  year  retrospecQve  review  (1975-­‐1992)  –  407  cases:  134  children,  273  adults    –  Incidence  in  children  declined  from  6.1/100,000  (1975-­‐78)  to  

0.3/100,000  (1989-­‐92)  –  Incidence  in  adults  increased  (0.78/100,000  to  2.9/100,000)  –  Adults  comprised  31%  of  cases  in  first  3  years  and  ;  97%  of  cases  in  last  

3  years,  with  no  pediatric  cases  in  the  last  2  yrs  

•  Similar  data  published  in  Australia  documenQng  shiv  from  a  pediatric  to  adult  disease  in  the  post  Hib  vaccine  era  (11)  

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Epidemiology  

•  Current  incidence  (3)  – adults  2-­‐3/100,000  – peds  0.3-­‐0.6/100,000  

•  For  adults:  (4)  –   peak  incidence:  35-­‐39  yr  age  group  – Male:female    is  2.5:1  – Mortality  rate:  1.2%-­‐7.1%  – Smoking  is  a  risk  factor  

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Microbiology  

•  PosiQve  blood  cultures  reported  in  12-­‐26%  adults  (3)  •  Bacteremia  less  common  in  adults  than  children  •  Variety  of  pathogens  in  adults:    

–  H.  influenza  –  Group  A  beta-­‐hemolyQc  Streptococcus  –  Non-­‐group  A  beta-­‐hemolyQc  Streptococcus  –  Staphylococcus  aureus  –  Streptococcus  pneumonia  –  Candida  albicans  –  Viral  

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Signs  &  Symptoms  

Adapted  from  (2)  

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Signs  &  Symptoms  

Adapted  from  (2)  

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Diagnosis—Sov  Tissue  Lateral  Neck  Xray  

•  Thickening  of  the  epiglo�s  present  on  73%-­‐86%  of  films  (3)  

•  Thumb  sign:  rounded  shape  of  the  epiglo�s  due  to  swelling  •  Vallecula  sign:  complete  or  parQal  obliteraQon  of  the  vallecula  

–  Be  wary  of  enlarged  lingual  tonsils  •  SensiQvity:    75%  •  ALL  PATIENTS  SHOULD  BE  ACCOMPANIED  TO  XRAY  

DEPARTMENT  WITH  EQUIPMENT  FOR  AND  PERSONNEL  TRAINED  IN  AIRWAY  MANAGEMENT  

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Epiglo�s  –  Sov  Qssue  xrays  

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Epiglo�Qs  –  Sov  Qssue  xrays  

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Diagnosis  in  Adults  

•  Laryngoscopy  in  adults  does  not  precipitate  acute  airway  obstrucQon  (2,3)  

•  FibreopQc  laryngoscopy  is  the  gold  standard(3,4)    •  Cherry  red  epiglo�s  is  the  classic  finding;  most  paQents  also  have  supraglo�c  inflammaQon  as  well  

•  No  complicaQon  of  nasal  flexible  laryngoscopy  in  small  case  series  of  adults  from  Australia  (5)  

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Epiglo�Qs  

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Epiglo�Qs/Supraglo�Qs  

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Treatment:      Adults  

•  No  consensus  on  airway  management  of  adult  epiglo�Qs.  •  Up  to  approximately  20%  require  airway  intervenQon;  hence  

all  require  admission  and  close  monitoring  with  airway  support  rapidly  available  (2,6)  

•  Risk  factors  that  predicted  need  for  aggressive  airway  management:  –  DYSPNEA  (6,  12)  

•  For  intubaQon:  ppv=62%,  npv=100%  (6)  

–  Stridor  (12,  13)  –  Muffled  voice  (12,  13)  

–  Diabetes  (12,  13)  –  Rapid  clinical  course  (ie  presented  <  12hrs  aver  symptom  onset)  (13)  

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Treatment:      Adults  

•  Admit  to  ICU  •  ENT  consult  •  Consent  done  for  possible  tracheostomy  •  Anesthesia  made  aware  •  High  dose  steroid  (Dexamethasone  10mg  IV  q6h)  

•  AnQbioQcs  

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Treatment:    Children  

•  Airway  should  be  secured  regardless  of  degree  of  apparent  respiratory  distress  (7,8)  

•  PaQent  should  not  be  moved,  reposiQoned  or  have  airway  examined  with  tongue  depressor  or  laryngoscope  

•  DefiniQve  airway  management:  –  Intubated  in  the  OR  with  ENT  present,  tracheostomy  set  open  and  

consent  signed  

•  Dexamethasone  •  AnQbioQcs  •  Swabs  done  at  intubaQon  

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Treatment:    AnQbioQc  Choice  (9,10)  

•  AnQbioQcs:  2nd  or  3rd  generaQon  cephalosporin  with  acQvity  against  beta-­‐lactamase  producing  H.  flu  –  Cefuroxime  

•  Adults:  0.75-­‐1.5  gm  IV  q8h  •  Peds:  50  mg/kg  IV  q8h  

–  Cefotaxime    •  Adults:  2-­‐3  gm  IV  q6-­‐8h  •  Peds:  50mg/kg  IV  q8h  

–  Cevriaxone  •  Adults:  1-­‐2  gm  IV  daily  •  Peds:  50  mg/kg  IV  daily  

•  AlternaQves  –  Ampicillin/Sulbactam  

•  Adults:  1.5-­‐3  g  IV  q6h  –  Ticarcillin/Clavulanate  

•  Adults:  3.1  g  IV  q4-­‐6h  –  Piperacillin/Tazobactam  

•  Adults:  3.375g  IV  q4-­‐6h  –  Levofloxacin  

•  Adults:    500mg  IV  daily  

–  GaQfloxacin  •  Adults:  400mg  IV  daily  

–  Trimethoprim/Sulfamethoxazole  

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•  Which  American  president  is  suspected  to  have  died  of  epiglo�Qs  despite  vigourous  bleeding  by  his  physicians?  

George  Washington  

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Case  

•  25  yr  old  male  – Sore  throat  for  3  days,  no  cough  – Normal  vitals,  afebrile  – Tonsillar  swelling,  erythema  and  exudate  – Tender  submandibular  nodes  

– Normal  voice,  no  trismus  – Should  he  get  anQbioQcs?  Steroids?  

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PharyngiQs  Clinical  

•  Clinical  differenQaQon  of  eQologic  organisms  virtually  impossible  

•  Hx  – Associated  symptoms  

•  Exam  – Airway  assessment  – Voice  changes  – Pharyngeal  erythema,  exudate  – Trismus  – Adenopathy  – Splenomegaly  

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PharyngiQs  DiagnosQc  Strategies  

•  GABHS  – Culture  – Rapid  DiagnosQc  Test  – Clinical  PredicQon  Rule  

•  Centor  score  (1981)  • Modified  Centor    (McIsaac  1998)  •  Simplified  Walsh  rule    (McGinn  2003)  

•  Mono  – Monospot  – VCA  

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PharyngiQs  Clinical  PredicQon  Rule-­‐  Modified  

Centor  

MacIsaac  et  al.    A  Clinical  Score  to  Reduce  Unnecessary  AnQbioQc  Use  in  PaQents  with  Sore  Throat.    CMAJ  1998;  158:  75-­‐83.  

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Modified  Centor  

Points   %  with  strep  infec%on  (+/-­‐  SD)  

LR   Post  test  probability  of  GABHS  assuming  prevalence  of  15%  

-­‐1  or  0   1  +/-­‐  0.8   0.05   1  %  

1   10  +/-­‐  3   0.52   8  %  

2   17  +/-­‐  4   0.95   14  %  

3   35  +/-­‐  5   2.5   31  %  

4  or  5   51  +/-­‐  6   4.9   46  %  

From    Evidence  Based  Emergency  Medicine.  1st  ediQon  2009.  p525  

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PharyngiQs  Clinical  PredicQon  Rule  –  Modified  

Centor  

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Simplified  Walsh  

McGinn  et  al.    ValidaQon  and  ModificaQon  of  Streptococcal  PharyngiQs  Clinical  PredicQon  Rule.    Mayo  Clin  Proc  2003;  78:  289-­‐293  

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Simplified  Walsh  

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Clinical  PredicQon  Rules  

•  “In  Summary,  there  are  a  variety  of  clinical  scoring  systems  available,  and  all  provide  modest  to  good  posiQve  and  negaQve  likelihood  raQos  for  the  diagnosis  of  strep  pharyngiQs,  and  are  thus  useful  guides  to  management”  

Evidence  Based  Emergency  Medicine  1st  ed  2009,  p  526  

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Rapid  Strep  Tests  

•  No  meta-­‐analyses  •  10  clinical  trials  •  7  guidelines  •  Insufficient  sensiQvity  to  be  used  alone  

•  Swab  technique  may  limit  accuracy  

•  EP’s  should  be  cauQous  in  their  use  of  rapid  strep  tests  and  use  in  conjuncQon  with  clinical  scores  to  increase  diagnosQc    accuracy  

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PharyngiQs    DiagnosQc  Strategies  

•  ProspecQve  cohort  study  – Primary  care  walk  in  clinic,  Geneva  – How  best  to  use  Centor  score,  RSAT  and  culture  – PharyngiQs  with  Centor  >2,  age  >  15  – 5  strategies  

• SymptomaQc  Rx  • SystemaQc  RSAT  • SelecQve  RSAT  Centor  =  2  or  3,  empirical  Abx  Centor=4  • Empirical  Abx  if  Centor  =  3  or  4  • SystemaQc  Culture  

Humair  et  al.    Management  of  Acute  PharyngiQs  in  Adults.    Arch  Intern  Med  2006;  166:  640-­‐644  

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PharyngiQs    DiagnosQc  Strategies  

•  Overall  prevalence  of  GAS  – 37.6%  

•  Centor  2   23.6%  •  Centor  3   41%  •  Centor  4   60.3%  

•  Compared  with  C&S,  RSAT  had  – SensiQvity   91.4%  – Specificity   95.3%  – PPV     92%  – NPV     95%  

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PharyngiQs  DiagnosQc  Strategies  

Humair  et  al.    Management  of  Acute  PharyngiQs  in  Adults.    Arch  Intern  Med  2006;  166:  640-­‐644.  

OpQmal  Abx  use  Most  expensive  Wait  for  C&S  results  Nearly  opQmal  Abx  use  

Cheapest  Immediate  decision  Best  Strategy  

Some  Abx  overuse  2nd  best  strategy  

High  anQbioQc  overuse  Some  underuse  

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PharyngiQs  DiagnosQc  Strategies  

•  Problems  – Not  an  emerg  populaQon  but  probably  not  that  different  from  our  pharyngiQs  paQents  

– Need  a  prospecQve  trial  looking  at  • Symptoms  • ComplicaQons  

• Our  health  care  se�ng  

– RSAT  NOT  available  at  TOH    – Is  available  at  some  community  hospitals  (Dr  Toye)  

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I D S A

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PharyngiQs  Treatment  

•  GABHS  – Penicillin  V  600mg  po  bid-­‐Qd  X  10d  – AlternaQve  for  pen  allergy  

•  Erythromycin,  azithromycin  •  Clindamycin  •  Cephalosporin  

•  SymptomaQc  treatment  – AnQpyreQcs,  analgesics  – Gargling  with  warm  saltwater?  – Drinking  warm  liquids?  

– CorQcosteroids  ?  

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CorQcosteroids  

•  SystemaQc  Review  and  Meta-­‐analysis  – 8  RCT’s  comparing  corQcosteroids  vs  placebo  

• Children  and  adults  • OutpaQent  se�ngs  • Steroids  

– Dexamethasone  up  to  10  mg,  prednisone  60  mg,  betamethasone  

– 6  trials  used  single  doses  • All  paQents  also  received  anQbioQcs  • Excluded  mono  • High  methodological  quality  

Hayward  et  al.    CorQcosteroids  for  pain  relief  in  sore  throat:  systemaQc  review  and  meta-­‐analysis.      BMJ  2009;  339:  b2976  

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CorQcosteroids  Meta-­‐analysis  Primary  outcomes  

NNT = 3.7

NNT = 3.3

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CorQcosteroids  Meta-­‐analysis  Primary  outcomes  

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CorQcosteroids  

•  Data  suggest  no  effect  in  mild  sore  throat  so  use  only  with  severe  or  exudaQve  sore  throat  

•  All  trials  include  anQbioQcs,  so  effect  of  steroids  alone  unknown  

•  Effects  most  apparent  in  iniQal  24  hrs,  implies  single  dose  sufficient  

•  Route  and  dose  not  fully  assessed  but  oral  likely  as  effecQve  as  IM  

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Cochrane  Review  AnQbioQcs  for  Sore  Throat  

•  27  studies,  updated  2006  •  Symptoms  

– Pain  and  fever  reduced  by  about  ½  by  anQbioQcs  – To  prevent  one  sore  throat  at  day  3,  NNT=6  – To  prevent  one  sore  throat  at  day  7,  NNT=21  – Subgroup  analysis  showed,  anQbioQcs  more  effecQve  at  day  3,  if  C&S  +  for  strep  • RR  0.58  (CI  0.48-­‐  0.71)  if  +  • RR  0.78  (CI  0.63-­‐0.97)  if  -­‐  

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Cochrane  Review  AnQbioQcs  for  Sore  Throat  

•  Non-­‐suppuraQve  complicaQons  – RheumaQc  fever  

• AnQbioQcs  reduced  by  >2/3  – RR  0.22  (CI    0.02-­‐2.08)  

– GlomerulonephriQs  • Trend  to  benefit  but  insufficient  cases  to  be  sure  

•  (classically  taught  that  Abx  not  effecQve)  

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Cochrane  Review  AnQbioQcs  for  Sore  Throat  

•  SuppuraQve  ComplicaQons  – AnQbioQcs  reduced  risk  of    

• AOM  – RR  0.30    (CI  0.15-­‐0.58)  

• SinusiQs  – RR  0.48    (CI  0.08-­‐2.76)  

• Peritonsillar  abscess  – RR  0.15  (CI  0.05-­‐0.47)  

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Cochrane  Review  AnQbioQcs  for  Sore  Throat  

•  Abx  confer  benefit    •  But  absolute  benefits  modest  

– Shorten  duraQon  of  symptoms  by  16  hrs    •  In  Western  society,  many  will  need  to  be  treated  with  Abx  to  benefit  few  for  suppuraQve  and  non-­‐suppuraQve  complicaQons  

•  Adverse  effects  – Diarrhea  – Rash  – resistance  

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GABHS  PharyngiQs  SuppuraQve  ComplicaQons  

•  Peritonsillar  abscess  – Quinsy  

•  Retropharyngeal  abscess  •  Other  Deep  space    neck  abscesses  •  SuppuraQve  cervical  lymphadeniQs  •  OQQs  media  •  SinusiQs  •  MastoidiQs  •  Lemierre’s    

– Jugular  venous  thromboplebiQs  

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PeritonsilliQs  

•  Peritonsillar  celluliQs  and  peritonsillar  abscess    – Clinical  conQnuum  – Most  common  deep  infecQon  of  H&N  in  adults  – CollecQon  of  pus  between  tonsillar  capsule  and  superior  constrictor  and  palatopharyngeus  muscles  

•  History  – PharyngiQs  symptoms  followed  in  2-­‐5  days  

•  Increased  odynophagia,  dysphagia  • drooling  

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Peritonsillar  Abscess  

•  Displacement  of  tonsil  medial  and  inferior  

•  Contralateral  uvula  deviaQon  

•  Trismus  •  Hot  potato  voice  •  Rancid  breath  

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Peritonsillar  Abscess  Treatment  

•  Drainage  –  Needle  aspiraQon  

–  Easier  than  I&D  with  simlar  outcome  –  ?ultrasound  guided  

–  I&D  •  CaroQd  artery  at  risk  •  At  TOH,  done  by  ENT    

•  AnQbioQcs  –  Penicillin  –  Macrolides  –  Clindamycin  –  Clavulin  

•  Fluids  if  dehydrated  •  Analgesia  

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Mono  

•  Epstein  Barr  Virus  (human  herpesvirus4  )  •  Spread  by  close  contact  •  1-­‐2  month  incubaQon  period  •  Classic  infecQous  mononucleosis  

– Fever,  malaise  – ExudaQve  pharyngiQs/tonsilliQs  – Lymphadenopathy  – Splenomegaly  – Atypical  lymphocytosis  – TransaminiQs  

•  In  older  adults  hepatomegaly  and  jaundice  

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Mono  

•  ComplicaQons  – Splenic  rupture  0.1-­‐  0.5%  – Autoimmune  hemolyQc  anemia  – Thrombocytopenia  – Neuro  rare  

• EncephaliQs,  meningiQs,  CN  palsies,  GBS  

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Mono  

•  Monospot  (Heterophil  anQbodies)  –  May  be  false  negaQve  in  the  1st  week  of  illness  –  Variability  with  age  in  paQents  with  mono  

•  Adults     95%  •  Children  >5   90%  •  Age    2-­‐4     75%  •  Age  0-­‐20  mo.     30%  

–  IgM  anQbodies  to  EBV  capsid  (VCA)  •  SensiQve     100%  •  Specific  •  Persist  4-­‐8wks  •  IgG  persist  life  long  •  Sent  to  CHEO  (EBV  Serology)  ,  2-­‐5  day  turnaround  

–  AnQbodies  to  EBV  nuclear  anQgen  develop  at  4-­‐6  weeks  and  persist  for  life  •  Peripheral  blood  smears  

–  Atypical  mononuclear  cells  in  75%  pts  –  2nd  or  3rd  week  of  illness  

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Ebell,  EBV  InfecQous  Mononucleosis.    American  Family  Physician  2004;  7:  1279-­‐87  

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Mono  

•  Treatment  – Mainly  supporQve  – CorQcosteroids  –  classic  indicaQons  

– Tonsillar  hypertrophy  that  threatens  airway  patency  – Severe  thrombocytopenia  – HemolyQc  anemia  

•  Prednisone  1-­‐2mg/kg/d  •  Evidence  is  contradictory  • Not  recommended  for  “rouQne”  IM  

– Avoid  contact  sports  •  Splenic  rupture  

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Thompson.    InfecQous  Mononucleosis  and  CorQcosteroids.    Archives  of  Otolaryngology-­‐  Head  and  Neck  Surgery  2005;  131:  900-­‐4.  

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Deep  Space  InfecQons  Neck  &  Face  

•  Spaces  – Peritonsillar  – Submandibular  – Parapharyngeal  – Retropharyngeal  – Danger  – prevertebral  

SomeQmes  referred  to  collecQvely  as    retropharyngeal  

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Deep  Space  InfecQons  Neck  &  Face  

•  Incidence  decreased  dramaQcally  –  Improved  dental  hygiene  – AnQbioQcs  

•  Risk  of  airway  compromise  – Airway  distorQon  – Trismus  

•  IntubaQon  – Awake  technique  preferable  – FibreopQc  best  – RSI  risky  

•  May  be  unable  to  intubate  and  venQlate  •  Only  if  double  set  up  ready  to  proceed  to  surgical  airway  

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Deep  Space  InfecQons  Neck  &  Face  

•  Submandibular  – Sublingual  &  Submaxillary  spaces  

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Ludwig’s  Angina  

•  Ludwig’s  angina  – CelluliQs  of  the  connecQve  Qssues  of  the  floor  of  the  mouth  and  neck  that  begins  in  the  submandibular  space  

– Polymicrobial  •  Mixed  oral  aerobic-­‐anaerobic  

•  Strep,  staph,  bacteroides,  H  flu,    pseudomonas,  klebsiella,  candida  

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Ludwig’s  Angina  

•  Causes  – Dental  disease  most  common  

– #  mandible  – LaceraQon  floor  of  mouth,  tongue  piercing  – Iatrogenic  

• TraumaQc  intubaQon  • Bronchoscopy  

– Spread  from  local  infecQon  

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Ludwig’s  Angina  

•  Symptoms  – Dysphagia,  odynophagia  – Neck  swelling  and  pain  – Dysphonia,  hot  potato  voice  – Fever  

•  Signs  – Bilateral  submandibular  swelling  – ElevaQon  and  woody  consistency  floor  of  mouth  – Tongue  elevaQon  – Bull  neck:    induraQon  and  edema  above  hyoid  – Tenderness  +/-­‐  subcut  emphysema  

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Ludwig’s  Angina  

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Ludwig’s  Angina  

• Mainly  clinical  diagnosis  •  US  useful  for  abscess  •  CT  and  MRI  for  complicaQons  

– Spread  to  other  deep  spaces  neck  – MediasQniQs,  empyema,  pericardiQs  – Internal  jugular  vein  thrombosis  (Lemierre’s)  – CaroQd  artery  infecQon,  erosion  – NecroQzing  fasciiQs  – others  

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Ludwig’s  Angina  

•  Management  – Airway  compromise  can  be  rapid  – FibreopQc  intubaQon    preferred  – If  surgical  airway  required,  may  need  trach  as  cricthyroidotomy  may  not  be  possible  

– AnQbioQcs  •  Penicillin  24MU  q  4h  +  metronidazole  1g  then  500mg  q6h  •  CefoxiQn  •  Clindamycin  •  Pip-­‐tazo  

– Surgical  drainage  if  not  responding  or  abscess  

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Deep  Space  InfecQons  Neck  &  Face  

•  Parapharyngeal  – CaroQd  artery  &jugular  vein  

– CN  IX,  X,  XI,  XII  – Cervical  sympatheQc  chain  

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Parapharyngeal  Abscess  

•  InfecQon  spread  from  – Odontogenic  – Pharyngotonsillar  – Others:      other  deep  space  neck  infecQons,  paroQQs,  sinusiQs,  infected  neck  tumors,  local  lymphadeniQs,  iatrogenic  from  nerve  block,  tonsillectomy  

•  polymicrobial  

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Parapharyngeal  Abscess  

•  Clinical  – Neck  pain  &  swelling,  

torQcollis  – Odynophagia  –  Fever  – Medial  tonsil  displacement  –  Posterolateral  pharyngeal  

wall  bulge  –  Trismus  

–  Tender  &  swelling  angle  of  mandible  

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Parapharyngeal  Abscess  

•  Xray  sov  Qssue  neck    – usually  not  helpful  

•  US,  CT,  MRI  

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Parapharyngeal  Abscess  

•  ENT  referral  for  surgical  drainage  •  IV  Abx  

– Same  as  ludwig’s  

•  ComplicaQons    – innumerable  

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Deep  Space  InfecQons  Neck  &  Face  

•  Retropharyngeal  – Base  of  skull  to  superior  mediasQnum  (T2)  – InfecQon  has  easy  access  to  mediasQnum  – Abscesses  tend  to  occur  lateral  to  midline  

•  Superior  constrictor  muscle  adheres  to  prevertebral  fascia  

•  Danger  – Extends  from  base  of  skull  to  diaphragm  – InfecQon  has  easy  access  to  mediasQnum  

•  Prevertebral  – Extends  from  base  of  skull  to  coccyx  – InfecQon  has  easy  access  to  mediasQnum  

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Deep  Space  InfecQons  Neck  &  Face  

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Retropharyngeal  InfecQons  

•  All  3  above  spaces  •  Children  <  6yrs  

– Prominent  retropharyngeal  nodes  that  can  get  infected  and  spread  

•  Adults  – Spread  from  nasopharyngiQs,  OM,  paroQQs,  tonsilliQs,  quinsy,  dental  infecQons,  ludwig’s,  parapharyneal  

– ComplicaQon  of  upper  airway  instrumentaQon  – FB  eg  fish  bones  – Hematologic  spread  – OsteomyeliQs,  disciQs  

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Retropharyngeal  InfecQons  

•  Usually  polymicrobial  – Aerobes  &  anaerobes  – TB  rare  

•  Clinical  – Sore  throat  – Dysphagia  – Odynophagia  – Neck  sQffness,  pain  – Fever  – Lump  in  throat  

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Retropharyngeal  InfecQons  

•  Clinical  – May  appear  quite  ill  – Dysphonia  

•  Cri  du  canard  – Neck  extended  – Prefer  supine  – Erythema,  edema,  mass  of  post  pharynx  – Tender  cervical  adenopathy  – Neck  swelling,  torQcollis  – Trismus  – Pain  on  rocking  larynx  /trachea  

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Retropharyngeal  InfecQons  

•  Diagnosis  – Xray  sov  Qssue  neck  

• >  7mm  at  inferior  aspect  2nd  vertebral  body  • At  inferior  aspect  6th  vertebral  body  

– >22mm  adults  

– >14  mm  children  

– CT  – MRI  

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Sov  Qssue  xray  

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CT  Neck  

Retropharyngeal  abscesses  

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Retropharyngeal  InfecQons  

•  Treatment  – Referral  to  ENT  for  drainage  – IV  ABX  

• Same  as  ludwig’s  

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Case    

•  42  yr  old  male    – Onset  typical  URTI  10  days  ago  – Was  resolving  but  last  2  days  

•  Fever  of  38C  •  Pain  over  lev  zygoma  •  Purulent  rhinorrhea  

– Wants  levaquin  like  last  Qme  he  had  sinusiQs  – Xray?  – AnQbioQcs?  Which  one?  – AdjuncQve  Rx  

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Sinus  Anatomy  

Frontal  sinus  

Maxillary  sinus  

Ethmoid  Sinuses  

Sphenoid  Sinus  

Sphenoid  Sinus  -­‐paired  -­‐opQc  nerve  &  CaroQd  artery  Occupy  lateral  walls  

Ethmoid  Sinuses  -­‐2  to  8  anterior  air  cells  -­‐1  to  8  posterior  air  cells  -­‐blood  supply  connects  With  ophthalmic  vessels      &Cavernous  sinus  -­‐Risk  of  spread  to  CNS  or  orbit  

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Sinus  Anatomy  

CT  Coronal  views  

OsQomeatal  complex:    area    where  the  maxillary,  anterior  ethmoid,  frontal  sinuses  drain,  Between    middle  &  inferior  turbinate  -­‐the  focal  point  for  sinus  disease  -­‐healthy  sinus  depends  on  patent  meatus  allowing  air  exchange  and  mucus  drainage  

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Pathophysiology  

• Most  common  causes  of  osQal  obstrucQon  – Viral  URTI  – Allergic  RhiniQs  

•  Increased  mucus  viscosity  and  ciliary  dysfuncQon  

• Bacteria  can  be  introduced  through  cough  and  nose  blowing    

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Pathophysiology  

•  Viral  URTIs  – 90%  have  element  of  viral  sinusiQs    – “rhinosinusiQs”  – O.5%  -­‐2%  viral  sinusiQs  complicated  by  bacterial  superinfecQon:  acute  bacterial  sinusiQs  

•  S.  pneumonia  •  H.  influenza  •  M.  catarrhalis  

– Chronic  sinusiQs  •  Anaerobic  •  Strep  species  •  S  .aureus  •  Fungi  

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Clinical  

•  Symptoms  – Nasal  congesQon  – Mucopurulent  discharge  – Nasal  obstrucQon  – Post  nasal  drip  – Fever  – Pain/pressure/headache  

• Maxillary:  zygoma,  teeth,  periorbital  •  Ethmoid:  medial  canthal,  periorbital  ,  temporal  •  Sphenoid:  vague  headaches  and  focal  points  anywhere  in  head  

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•  Symptoms  – Typically  7-­‐10  days  – IniQal    5-­‐7  days  difficult  to  differenQate  viral  from  bacterial  

– Worsening  aver  5  days  or  persistent  aver  10  days  • Suggests  bacterial  • “double  sickening”  

– Pt  improves  iniQally  &  then  worsens  

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Independent  Predictors  of  SinusiQs  

Likelihood  Ra%o  (95%  CI)   LR  (95%  CI)  

PosiQve   NegaQve  

Maxillary  toothache   2.5    (1.2-­‐5.0)     0.9  (0.8-­‐1.0)  

Purulent  SecreQons   2.1    (1.5-­‐3.0)   0.7  (0.5-­‐0.8)  

Poor  response  to  decongestants  

2.1    (1.4-­‐3.1)   0.7    (0.6-­‐0.9)  

Abnormal  transilluminaQon   1.6    (1.3-­‐2.0)   0.5    (0.4-­‐0.7)  

History  of  coloured  nasal  discharge  

1.5    (1.2-­‐1.9)   0.5    (0.4-­‐0.8)  

Evidence  Based  Emergency  Medicine,  1st  ed,  p536  

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Likelihood  of  Acute  SinusiQs  

Number  of  Signs  &  Symptoms   Likelihood  Ra%o  

4   6.4  

3   2.6  

2   1.1  

1   0.5  

0   0.1  

Evidence  Based  Emergency  Medicine,  1st  ed,  p536  

Authors  suggested    -­‐no  xray  for  score  of  0,  1,  4  -­‐xray  for  score  of  2,3  

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InvesQgaQons  

•  Xray  –  Poor  for  ethmoid  or  sphenoid  sinusiQs  –  PosiQve  findings  

•  Sinus  opacificaQon  •  Air  fluid  level  •  Mucosal  thickening  >  6  mm  

– Common  in  asymptomaQc  paQents  

–  NOT  rouQnely  –  Limit  to    

•  quesQonable  diagnosis  •  Unresponsive  to  treatment  

•  CT  –  NOT  rouQnely  –  For  complicaQons  

•  Cultures  of  nasopharynx  –  NOT  unless  toxic  or  immunocompromised  

•  Gold  standard:  sinus  aspiraQon  –  Rarely  done  

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Right  maxillary  sinus  opacificaQon   Lev  maxillary  sinus  air/fluid  level  

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Coronal  CT  showing  right  maxillary  And  ethmoid  opacificaQon,  lev      Maxillary  sinus  air-­‐fluid  level  

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Management  

•  Large  proporQon  resolve  spontaneously  •  AnQbioQcs:  

–  Cochrane  Review  for  cure  •  Penicillin  vs  Placebo  RR  1.72  (95%CI  1.00-­‐2.96)  •  NNT  7  

–  Not  improving  aver  7  days  –  Moderate  to  severe  symptoms  of  any  duraQon  

•  1st  line  –  Cochrane  Review:    

•  No  difference  between  – Newer  non  penicillins  vs  penicillins  (RR  1.01,    95%CI  0.97-­‐1.04)  – Newer  non  penicillins  vs  clavulin  (  RR  0.98,  95%CI  0.95-­‐1.01)  

–  Amoxicillin  •   10  days  advised    by  IDSA  guidelines  •  Evidence  to  suggest  shorter  (5-­‐7days)  equivalent  to  longer  Rx  

–  TMP/Sulfa  

•  2nd  line  –  Clavulin  –  Cefuroxime  axeQl  –  Clindamycin  +/-­‐  cipro,  septra,  macrolide  

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Management  

•  Decongestants  –  Cochrane  review:  insufficient  data  –  Topical  maximum  3-­‐5days  to  avoid  rebound  –  ?oral  decongestants  – Oral  anQhistamines  for  allergic  rhinosinusiQs  only  

•  Inhaled  steroids  –  Cochrane  review  for  resoluQon  or  marked  improvement  of  

symptoms  with  various  doses  •  RRR  1.11  (95%CI:  1.04-­‐1.18)  •  NNT=7  

•  Sphenoid  or  Frontal  sinusiQs  with  air/fluid  levels  may  require  hospitalizaQon  

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ComplicaQons  

•  Spread  to  bones  and  sov  Qssue  face  and  orbit  – Facial  and  periorbital  celluliQs  – Periorbital  abscess  – OpQc  neuriQs  – Orbital  abscess  

•  Intracranial  – MeningiQs  – Cavernous  sinus  thrombosis  – Empyema  and  brain  abscess  

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Summary  

•  Pneumonia  –  IDSA/ATS  2007  guidelines  –  DisposiQon  tools  –  Recommended  AnQbioQcs  

•  AspiraQon  pneumoniQs  vs  pneumonia  

•  Pneumothorax  –  Types  &  Size  esQmaQon  –  ACCP  vs  BTS  guidelines    

•  Acute  BronchiQs  •  Pleural  Effusions  

–  ExudaQve  vs  TransudaQve  •  Hemoptysis  approach  

•  Supraglo�Qs  –  Change  from  peds  to  adults  –  Diagnosis  and  Treatment  

•  PharyngiQs  –  Clinical  predicQon  rules  –  Rapid  strep  tests  –  Quinsy,  mono  

•  Deep  Space  Neck  InfecQons  –  Submandibular  –  Parapharyngeal  –  Retropharyngeal  

•  SinusiQs  –  Clinical  diagnosis