FIBEROPTIC BRONCHOSCOPY and BRONCHOALVEOLAR LAVAGE FOR THE EVALUATION OF PULMONARY DISEASE in IMMUNOCOMPROMISED CHILDREN - PowerPoint PPT Presentation

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FIBEROPTIC BRONCHOSCOPY and BRONCHOALVEOLAR LAVAGE FOR THE EVALUATION OF PULMONARY DISEASE in IMMUNOCOMPROMISED CHILDREN

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Title: FIBEROPTIC BRONCHOSCOPY and BRONCHOALVEOLAR LAVAGE FOR THE EVALUATION OF PULMONARY DISEASE in IMMUNOCOMPROMISED CHILDREN


1
FIBEROPTIC BRONCHOSCOPY and BRONCHOALVEOLAR
LAVAGE FOR THE EVALUATION OF PULMONARY DISEASE in
IMMUNOCOMPROMISED CHILDREN
E Yalçin, U Özçelik, D D Ersöz, N Çobanoglu, S
Pekcan, M Köse, T Öcal, Ö Sanal, N Kiper
Hacettepe University Faculty of
Medicine Pediatric Chest Diseases
Unit, Anestesiolgy and Reanimation
Department, Pediatric Immunology
Unit. 06100-Sihhiye, Ankara.
2
Patients with childhood cancer or primary
immunodeficiencies (PID) are at high risk for
developing pulmonary infections and
non-infectious complications. An appropriate
diagnosis may be achieved in these situations by
fiberoptic bronchoscopy (FB) and bronchoalveolar
lavage (BAL).
3
  • The overall daignostic rate achieved by FB and
    BAL investigations in immunocompromised patients
    was 84.
  • A definite organism was recovered in 53.
  • The rate of complications was 30.

4
  • 95 immunocomprimised patients receiving a regimen
    of broad spectrum ab and antifungal egents
  • - Respirator pathogenes were detected only in
    BAL of 29 of the 95 patients (30)
  • - Pathogens detected only in the BAL fluid were
    not susceptible to a standart broad spectrum
    antibiotic and antifungal regimen in 12 of the 29
    patients (41).
  • FB and BAL give important informations in
    immunocompromised patients even if they were
    given ab and antifungal therapy.

5
AIM
To evaluate the yield of FOB and BAL in these
children with pulmonary disease
6
PATIENTS AND METHODS
To evaluate the yield of FOB and BAL in these
children with pulmonary disease, The medical
records of 16 immunocompromised children aged 3.5
months to 14 yrs (mean 4.7 yrs) between 2000 and
2007 were retrospectively reviewed.
7
PATIENTS AND METHODS
Fiberoptic bronchoscopy with BAL was performed
with 5.2, 4 or 3.6-mm pediatric flexible
bronchoscope (Olympus BF-P200 Evis
bronchovideocsope/ Olympus BF-3C30 Olympus, New
Hyde Park, NY). Propofol was given for sedation
(Diprivan, Zeneca-Abdi Ibrahim, 1-1.5 mg/kg,
i.v.). Heart rate and transcutaneous oxygen
saturations were monitored throughout the
procedure (Sein Patient Monitor-SE 485).
Topical anesthesia of the upper and lower airways
was performed by 2 lidocaine. BAL was
performed either in an area most prominently
affected on the HRCT or in the right middle lobe
by gently wedging the tip of the bronchoscope in
a segmental bronchus. Three 1-mL/kg aliquouts
of sterile saline warmed at 370C were instilled
through the instrumentation channel.
8
PATIENTS AND METHODS
  • Each aliquot was immediately aspirated into a
    steril specimen container using a wall suction
    pressure of 100 to 120 mm Hg.
  • The first aliquot of the recovered BAL fluid
    was discarded all other samples were pooled for
    analysis.

9
PATIENTS AND METHODS
  • The BAL fluid samples were analysed for total
    and differential cell counts.
  • Aerobic and anaerobic cultures as well as
    cultures for tuberculosis and fungi were
    performed.
  • Lipid laden and hemosiderin laden macrophages
    were also investigated.
  • If purulan secretions was observed and/or
    culture positivity was detected in BAL fluid,
    presence of infection wass accepted.

10
PATIENTS
Diagnosis No of Patients SCID 8 (2/8
BMT) CVID 2 ALL 2 HL 1 CGD 1 CD8 ? 1
Vasculitis 1
Early bronchoscopy could not performed in these
patients, because they had severe respiratory
distress and/or thrombocytopenia. So, almost all
the patients were receiving empiric therapy
while bronchoscopic studies were performed.
11
PATIENTS
HRCT Findings No of Patients Diffusef/local
noduler infiltrations 5 Consolidation and/or
atelectasis 5 Diffused interstitial
infiltrations 4 Diffused ground glass opacities
2
12
SONUÇLAR
HRCT Findings FB BAL results Diffusef/local
noduler infiltrations Pu (1/5) 1 PCP, 2 fungal
pneumonia, 1hemorrhage (n5) Hemorrhage
(C.albicans and A.fumigatus) (1/5) Consolidat
ion and/or atelectasis Pu (2/5) 2 bacterial
pneumonia (n5) (H.inf ve P.aerugin) Diffuse
d interstitial infiltrations Pu (3/4) 1 CMV, 1
PCP, 1 A.fumigatus (n4) Diffused ground
glass opacities Normal - (n2)
13
Tani Takayasu vasculitis X-ray and HRCT
Diffused intestitiel infiltrations BAL PCP
Fluorescein-labeled antibody method
14
RESULTS .I.
  • The overall diagnostic rate achieved in children
    was 68 with FB-BAL. .
  • Microorganisms were detected in all patients
    observed purulant secretions.
  • The results of the FB-BAL changed therapeutic
    decision in 7 patients (43) exactly
  • - Pulmonary hemorrhage (n1)
  • - PCP (n2)
  • - Fungal infections (n3)
  • - CMV infection (n1)

15
RESULTS .II.
  • No significant adverse events were observed
    after the procedure.
  • Sensitivity of HRCT findings in estimate of
    etiology
  • was weak other than bacterial pneumonia.
  • Mean 2.5 years follow-up, mortality rate was
    found as 18.

16
DISCUSSION
  • Early bronchoscopy could not performed in these
    patients, because they had severe respiratory
    distress and/or thrombocytopenia. So, almost all
    the patients were receiving empiric therapy
    while bronchoscopic studies were performed.
  • Therefore, the yield of this procedure was low in
    our retrospective study.
  • FB and BAL should be considered as an initial
    diagnostic tool in pediatric immunocompromised
    patients with pulmonary complications, if the
    patients condition suitable.
  • When this safe procedure could be done early, it
    will prevent unnecessary use of drugs which have
    often side effects and high cost.
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