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TB
PERTUSIS
NEOPLASM (BENIGN & MALIGNANT)
BRONKIEKTASIS
Dilatasi irreversibel dari cabang
bronkial.
Biasanya disertai dengan produksi
sputum purulen yang kronik dan
hemoptisis.
Dapat diperiksa dengan CT scan
(high resolution) atau
trakeobronkografi.
BRONKIEKTASIS
POSTINFLAMMATORY
Inflamasi sekresi cairan stasis infeksi (RSV,
pertusis, rubella, & tuberkulosis) gangguan pada
dinding bronkus dilatasi dan distorsi
OBSTRUKTIF
Lesi obstruktif : tumor, benda asing di bronkus,
kompresi ekstrinsik, impacted mucus
KONGENITAL
Jaringan bronkial & atresia, sindrom cilia immotil,
cystic fibrosis, dan sindrom yang berhubungan
dengan kelainan formasi kartilage (sindrom William
Campbell, sindrom Mounier-Kuhns)
BRONCHIECTASIS
Definition
irreversible dilatation of airways due
to inflammatory destruction of
airway walls resulting from
persistently infected mucus
usually affects medium sized airways
P. aeruginosa is the most common
pathogen
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & US
R11 Respirology: Disease of Airway Obstruction, Bronchiectasis (page 1259)
BRONCHIECTASIS
Obstructio Post-infection
n
(results in dilatation
of bronchial walls)
Tumour
Pneumonia
Hypogammaglobulinemia
Foreign
body
TB
CF
Thick
mucus
Measles
Pertussis
Allergic
bronchopulmonary
aspergillosis
MAC (mycobacteria
avium complex)
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & US
R11 Respirology: Disease of Airway Obstruction, Bronchiectasis (page 1259)
BRONCHIECTASIS
Signs and Symptoms
chronic cough, purulent sputum (but
10-20% have dry cough), hemoptysis
(can be massive), recurrent
pneumonia, local crackles
(inspiratory and expiratory), wheezes
clubbing
may be difficult to differentiate from
chronic bronchitis
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & US
R11 Respirology: Disease of Airway Obstruction, Bronchiectasis (page 1259)
BRONCHIECTASIS
Investigations
PFTs: often demonstrate obstructive pattern but may
be normal
CXR
nonspecific: increased markings, linear atelectasis, loss
ofvolume in affected areas
specific: "tram tracking" - parallel narrow lines radiating from
hilum, cystic spaces, honeycomb like structures
BRONCHIECTASIS
Treatment
vaccination: influenza and Pneumovax
antibiotics (oral, IV, inhaled)- routinely used for mild
exacerbations, driven by sputum
sensitivity; macrolides may be used chronically for an antiinflammatory effect
inhaled corticosteroids - decrease inflammation and
improve FEY1
oral corticosteroids for acute, major exacerbations
chest physiotherapy, breathing exercises, physical exercise
pulmonary resection: in selected cases with focal
bronchiectasis
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & US
R11 Respirology: Disease of Airway Obstruction, Bronchiectasis (page 1259)
TUBERCULOSIS (TB)
Etiology, Epidemiology and Natural History
Mycobacterium tuberculosis: slow growing aerobe
(doubling time = 18 h) that is capable of intracellular
survival because it replicates in macrophages
5% of primary infections lead to progressive primary
disease
95% of primary infections lead to latent TB
1/3 of the world's population is infected with latent TB
5-10% of those infected with latent TB experience
reactivation disease, most often within the first 2 years
of infection.
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & US
ID24 Infectious Disease: Systemic Infection, Tuberculosis (TB) (page 631-632)
TUBERCULOSIS (TB)
Risk Factors
for exposure/infection
travel or birth in country with high TB prevalence (e.g. Asia, SubSaharan Africa)
aboriginal, crowded living conditions, low SES/homeless
personal or occupational contact
see Canadian Tuberculosis Standards by Public Health Agency of
Canada for more information on at risk populations
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & US
ID24 Infectious Disease: Systemic Infection, Tuberculosis (TB) (page 631-632)
TUBERCULOSIS (TB)
Clinical Features
ii. miliary TB
iii. extrapulmonary TB
TUBERCULOSIS (TB)
Investigations
PPD/Mantoux skin test: positive
result only indicates infection, not
active disease (PPD is not used to
diagnose or exclude active TB)
IFN- release assay
If induration at 4872 h
> 5 mm if immunosuppressed,
close contact with active TB,
CXR fibrocalcific disease, with
HIV-positive or if using anti-TNF
blockers
> 10 mm all others; decision to
treat depends on individual risk
factors
in patients previously infected with TB, False -: poor technique, anergy,
malignancy, infection < 10 wks
T-cells produce increased amounts of
ago or remotely
IFN- when re-exposed to TB antigen
False +: BCG after 12 months of
age in a low-risk individual
detects antigen not in the BCG vaccine Booster effect: initially false result boost to a true + result by
or non-tuberculous mycobacteria
the testing procedure itself
(NTM), therefore fewer false positives
(usually if patient was infected
not currently recommended for routine long ago so had diminished
delayed type hypersensitivity
screening, but may be useful in skin
reaction or if history of BCG)
PPD: purified
protein
derivative
test positive
with
low pretest
Torontopatient
Notes 2012,
Comprehensive
Medical Reference
& Review
for MCCQE
I & US
ID24 Infectious Disease: Systemic Infection, Tuberculosis (TB) (page 631-632)
TUBERCULOSIS (TB)
Investigation
CXR
TUBERCULOSIS (TB)
Prevention
Prevention of infection : BCG vaccine
~80% effective against pediatric miliary and meningeal TB
effectiveness in adults debated (anywhere from 0-80%)
routine use rarely recommended in Canadian populations
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQ
USMLE II :
TUBERCULOSIS (TB)
Treatment of Active Infection
empiric therapy: INH + rifampin + pyrazinamide
+ ethambutol + pyridoxine
pulmonary TB: INH + rifampin +pyrazinamide+
pyridoxine x 2 months (initiation phase), then INH
+ rifampin +pyridoxine x 4 months in fully
susceptible TB (continuation phase), total 6
months
extrapulmonary TB: same regimen as pulmonary
TB but increase to 12 months in bone/joint, CNS,
and miliary/disseminated TB +corticosteroids for
meningitis, pericarditis
empiric treatment of suspected MDR (multidrug
resistant) or XDR (extensively drug-resistant) TB
requires referral to a specialist
Treatment of Active
TB
RIPE
Rifampin
Isoniazid (INH)
Pyrazinamide
Ethambutol
PERTUSSIS
Bordetella pertussis, whooping cough, "100day cough
incubation: 6-20 d; infectivity: 1 wk before
paroxysms to 3 weeks after
increase in number of reported cases since
early 1990s
spread: highly contagious via air droplets
released during intense coughing
greatest incidence among children <1 yr
and adolescents
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & USM
P58 Pediatrics: Infectious Disease, Pertussis (page 1090)
PERTUSSIS
Clinical Presentation
Paroxysmalstage
2-4wks
paroxysms of cough, sometimes followed by inspiratory whoop (whoop
may be absent in children <6 months or adults)
infants may present with apnea
vomiting with coughing spells
onset of attacks precipitated by yawning, sneezing, eating, physical
exertion
can have severe symptoms for 6 wks, cough for 6 months
pressure effect - subconjunctival hemorrhage, rectal prolapse, hernias,
epistaxis
convalescent stage
1-2wks,noninfectious
occasional paroxysms of cough, but decreased frequency and severity,
Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
lasts up Toronto
to 6 months
P58 Pediatrics: Infectious Disease, Pertussis (page 1090)
PERTUSSIS
Diagnosis
Clinical: URTI symptoms followed by
paroxysms of cough in an afebrile
child
Lymphocytosis
PCR of nasopharyngeal swab or
aspirate
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
P58 Pediatrics: Infectious Disease, Pertussis (page 1090)
PERTUSSIS
Complications
otitis media
respiratory complications
sinusitis, secondary pneumonia, atelectasis,
pneumomediastinum, pneumothorax,
interstitial or subcutaneous emphysema
secondary to ruptured alveoli
neurological complications
seizures, encephalopathy (1:100,000),
intracranial hemorrhage
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
P58 Pediatrics: Infectious Disease, Pertussis (page 1090)
PERTUSSIS
Treatment
supportive care
hospitalize if paroxysms of cough are associated with cyanosis
and/or apnea and give O2
antimicrobial therapy indicated if B. pertussis isolated, or
symptoms present for <21 d
azithromycin 10 mg/kg/d x 5 d, erythromycin 40-50 mg/kg/d x 14 d or
clarithromycin 15 mg/kg/d x 7 d
isolate until 5 d of treatment
treatment will decrease infectivity and symptom severity but not change
course of illness
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
P58 Pediatrics: Infectious Disease, Pertussis (page 1090)
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
R29 Respiratory: Neoplasm, Benign Lung Tumours (page 1277)
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
R29 Respiratory: Neoplasm, Benign Lung Tumours (page 1277)
bronchial carcinoids
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
R29 Respiratory: Neoplasm, Benign Lung Tumours (page 1277)
MALIGNANT LUNG
TUMOURS
Pathological Classification
bronchogenic cancer (90% ofprimary lung cancers,
see Table 27)
classified into small cell lung cancer (SCLC) and nonSCLC (NSCLC, e.g. adenocarcinoma,
squamous cell, large cell), bronchioalvelolar cancer
(BAC)
incidence of adenocarcinoma is increasing
lymphoma
secondary metastases: breast, colon, prostate,
kidney, thyroid, stomach, cervix, rectum, testes,
bone, melanoma
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
R29 Respiratory: Neoplasm, Malignant Lung Tumours (page 1278)
Characteristic of Bronchogenic
Cancer
Cell Type
Incidence
Correlatio
n
with
Smoking
Location
Histology
Metastasi
Adenocarci
noma
M:35%
F:40%
Weak
Peripheral
Glandular,
mucin
producing
Early,
distant
Squamous
Cell
Carcinoma
(SCC)
30%
Strong
Central
Keratin,
intercellula
r bridges
Local
invasion
and distant
spread,
may
cavitate
SCLC
25%
Strong
Central
Oat cell,
neuroendo
crine
Disseminat
e at
presentatio
n
Origin in
endobronc
hial cells
Large cell
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
10-15%
Strong
Peripheral
Anaplastic,
R29 Respiratory:
Neoplasm, Benign
Lung Tumours
(page 1278) Early,
MALIGNANT LUNG
TUMOURS
Risk Factors
cigarette smoking: 85% of lung cancer related to smoking
asbestos 5x increased risk, asbestos+ smoker 80-90x
increased risk
radiation: radon, uranium (especially if smoker)
arsenic, chromium, nickel exposure
genetic damage
parenchymal scarring: granulomatous disease, fibrosis,
scleroderma
passive exposure to cigarette smoke
air pollution: exact role is uncertain
HIV
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
R29 Respiratory: Neoplasm, Benign Lung Tumours (page 1278)
MALIGNANT LUNG
TUMOURS
Signs and Symptoms
cough (75%): beware of chronic cough that
changes in character
dyspnea (60%)
chest pain (45%)
hemoptysis (35%)
other pain (25%)
clubbing(21%)
constitutional symptoms: anorexia, weight
loss, fever, anemia
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
R29 Respiratory: Neoplasm, Benign Lung Tumours (page 1278)
Presentation
pericardium
Esophageal compression
dysphagia
Phrenic nerve
Paralyzed diaphragm
hoarseness
erosion
Toronto
2012,
Comprehensive Medical Reference & Review for MCCQE I & U
Distant metastasis
toNotes
brain,
bone,
R29 Respiratory: Neoplasm, Benign Lung Tumours (page 1278)
MALIGNANT LUNG
TUMOURS
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
R29 Respiratory: Neoplasm, Benign Lung Tumours (page 1279)
MALIGNANT LUNG
TUMOURS
Investigations
Initial diagnosis
imaging: CXR, CT chest + upper abdomen, PET scan,
bone scan
cytology: sputum
biopsy: bronchoscopy, percutaneous, mediastinoscopy
Staging work-up
blood work: electrolytes, LFTs, calcium, ALP
maging: CXR, CT thorax and upper abdomen, bone
scan, neuroimaging
invasive: bronchoscopy, mediastinoscopy,
mediastinotomy, thoracotomy
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
R29 Respiratory: Neoplasm, Benign Lung Tumours (page 1279)
MALIGNANT LUNG
TUMOURS
Therapy for Bronchogenic Cancer
Surgery
not usually performed for SCLC since is
generally non-curable
preferred treatment ofstage I and II NSCLC is
resection with a curative intent
advanced NSCLC (stage III and IV) is often
palliated with chemotherapy and/or radiation
contraindications:
spread to contralateral lymph nodes or distant sites
- patients with surgically resectable disease must undergo
mediastinal node sampling since CT thorax is not accurate
in 20-40% ofcases
poor pulmonary status (e.g. Toronto
unable
to2012,
tolerate
resection
Notes
Comprehensive
Medical
Reference
&
Review
for
MCCQE
I
&
USMLE
II :
oflung)
R29 Respiratory: Neoplasm, Benign Lung Tumours
(page 1280)
MALIGNANT LUNG
TUMOURS
chemotherapy (no role for chemo alone, only in
combination with other treatments)
cisplatin and etoposide
paclitaxel, vinorelbine, and gemcitabine are newer NSCLC
therapies
new biologics, e.g. epidermal growth factor inhibitor (gefitinib)
Complications:
acute: tumour lysis syndrome, infection, bleeding, myelosuppression,
hemorrhagic cystitis (cyclophosphamide), cardiotoxicity (doxorubicin),
renal toxicity (cisplatin), peripheral neuropathy (vincristine)
chronic: neurologic damage, leukemia, additional primary neoplasms
Radiotherapy
Palliative care for end-stage disease
Toronto Notes 2012, Comprehensive Medical
Reference & Review for MCCQE I & USMLE II :
R29 Respiratory: Neoplasm, Benign Lung Tumours
(page 1280)
Toronto Notes 2012, Comprehensive Medical Reference & Review for MCCQE I & U
R29 Respiratory: Neoplasm, Approach to the Solitary Pulmonary Nodule (page 127