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Dyspnea

ARIF SATRIA SUSILO TARIGAN


2208260076
Patofisiologi sesak napas
Differences Shortness of breath

Channel Pleura
Asthma, COPD, TB, Pulmonary Pleural effusion, pneumothorax, pulmonary edema
Thromboembolism

parenkim vascular
Pneumonia CHD, CHF, Pulmonary embolism
ASTHMA

Asthma is an intermittent and reversible airflow


disorder that only affects the airways, not the alveoli

Etiology : - respiratory tract infections


- obesity
- genetic
- cigarette smoke
- emotional factors or stress
- use of aspirin, beta blockers
ASTHMA
ASTHMA
Additional Complaints: Diagnostic examination results:
● Cough ● Inspection: Symmetrical chest movement, if it gets
● Increased Phlegm worse, chest retraction +
● Chest feels heavy ● Palpation: Stem Fremitus is normal
● Recurring Symptoms ● Percussion: normal
● Gets worse at night ● Auscultation: Expiratory wheezing +
● wheezing
ASTHMA
X-ray:
● There was thickening of the bronchial walls
Laboratory: ● Bronchial dilatation
● Eosinophils increased (>4%) ● Cylindrical bronchiectasis from varicose veins
● Total Serum IgE level >100IU ● Mucoid impaction of the bronchi
● AGDA: PaCO2 > 45 mmHg ● There is air trapping
● Mosaic pulmonary ateunation pattern
Cypometry:
normal FEV/FVC >75% post bronchodilator
ASTHMA
Treatment
ASTHMA
Form of providing education:
● Communication/advice during
Education for sufferers/families aims to: treatment.
• increase understanding (about asthma in general ● Lecture
• general and pattern of asthma itself) ● Exercise/training
• improve skills (ability in handling ● Supervision
• asthma) ● Discussion
• increase satisfaction ● Exchange of information (sharing
• increase self-confidence of information group)
• increasing compliance and independent handling. ● Presentation films/videos
● Leaflets, brochures, reading
books
● Etc
COPD

COPD is a chronic inflammatory disease


characterized by persistent respiratory symptoms and
airflow limitation due to disruption of the alveoli.

Etiology : - respiratory tract infections


- obesity
- genetic
- cigarette smoke
- emotional factors or stress
- use of aspirin, beta blockers
COPD
COPD
Additional Complaints: Diagnostic examination results:
● Cough ● Inspection: pursed lip breathing, barrel chest, pink
● Increased Phlegm puffer, blue bloater, use of assisted breathing muscles
● Chest feels heavy when ● Palpation: Stem Fremitus decreases, ICs widen
breathing ● Percussion: hypersonor, heart border <<
● Auscultation: vascular/decreased breath sounds,
rhoki+, prolonged expiration, heart sounds <<
COPD
Laboratory: X-ray:
● Increased monocytes (N: 2-11) Emphysema-hyperinflation
● Eosinophils increased (N: 0-5 Hyperlucency
● AGDA: PaCO2 increases (22-26), PO2 ICS widens
decreases (22-26) The diaphragm is horizontal
Bronchovascular-normal/
bronchovascular pattern
COPD
Pulmonary embolism
Pulmonary embolism is an infarction of lung tissue
due to blockage of the pulmonary artery due to an
embolic event

Etiologi : migration of thrombus from other parts of


the body
Pulmonary embolism
Pulmonary embolism
Additional Complaints: Diagnostic examination results:
● Inspection: cyanosis, pale
● Pleuritic pain ● Palpation: stem fremitus descends
● Cough ● Percussion: Faint
● Swelling of the lower limbs ● Auscultation: Rhonki +, Gallop
● Bleeding cough ● Temperature >35 C
● Shivering ● Respiratory frequency >20x/i
● Fever ● Pulse Frequency 100x/i
● cyanosis
Pulmonary embolism
Laboratory: Xray :
• AGDA  PCO2 <35 mmHg

● Cardiomegaly
Plasma D-Dimer levels increase
• Leukocytes increase ● The presence of Kerley B lines in the
• Troponin increases interlobes
● Bilateral infiltration with butterfly
pattern
Pulmonary embolism
Pneumonia
Etiology :

Pneumonia is a common acute respiratory


infection that attacks the alveoli and distal
bronchial tree of the lung.

The disease is broadly divided into


community-acquired pneumonia (CAP) or
hospital-acquired pneumonia (HAP, which
includes ventilation-associated pneumonia
(VAP)
Pneumonia
Pneumonia
Additional Complaints: Diagnostic examination results:
● Breathing >30 times / minute
● Fever ● Systolic blood pressure < 90 mmHg
● Shivering ● Temperature <35 C or > 40 C
● Sweating ● Pulse >125 x/minute
● Cough with bloody phlegm
● Pleurisy pain
Pneumonia
Laboratory : Xray :
● Infiltrate until consolidated with air
• AGDA  PH 7.35 bronchogram
• Sodium < 130 mEq/liter ● Bronchogenic spread
• Hematocrit <30% ● Interstitial and cavity images
• PO2 <60 mmHg
Pneumonia

INITIAL PROCEDURE
Outpatients:
1. healthy: Azithromycin 500 mg orally 1x1
2. Comorbid: Levofloxacin 750 mg orally or Amoxicillin/Clavulanate orally 2gr 2x1
Non-ICU inpatients: Levofloxacin 750 mg orally or IV or Ceftriaxone 1-2gr IV + Azithromycin
orally or IV 1gr 1x1
ICU inpatients: Ceftriaxone 2 gr IV + Azithromycin or Levofloxacin 750 mg orally
Patients suspecting Pseudomonas infection: Meropenem 1gr IV 3x administration +
Ciprofloxacin 400mg IV 2x administration or Levofloxacin 750mg IV
Patients suspecting MRSA infection: Linezolid 600mg IV 2x administration or Vancomycin
15mg/kgBB 2x administration
Pneumothorax
Pneumothorax is the accumulation of air or gas in the pleural
cavity

Etiology:
1. Spontaneous pneumothorax
- Primary pneumothorax: occurs without underlying lung
disease
- Secondary pneumothorax: complications of previous lung
disease

2. Traumatic pneumothorax
Occurs as a result of traumatic injury

3. Pneumothorax due to pressure


Excessive pressure on the lung causes it to collapse
Pneumothoraks
Pneumothoraks
Additional Complaints: Diagnostic examination results:
● Inspection: asymmetric chest wall movement
● Sharp pain when inhaling ● Palpation: stem fremitus descends
● Chest feels narrow ● Percussion: hypersonor
● Tired easily ● Auscultation: vesicular disappeared
● Cyanosis
● Tachycardia
Pneumothoraks
Laboratory : Xray :
● Pleura line +
• Mild Leukocytes ● Hyperlucency
• AGDA: PO2 increases, ● The mediastinal heart is pushed
PCO2 decreases towards healthy lungs
● The diaphragm is pushed down

Treatment :
• Needle thoracocentesis : ICS II Linea midclavicularis

• Chest tube/WSD : ICS V Linea midaxillaris


Pleura effusion

Pleural effusion is a buildup of fluid in the pleural space which


is located between the visceral and parietal surfaces
Etiology:
1. Viruses and mycoplasma
The types of viruses are: echo virus, rickettsia, mycoplasma,
chlamydia.
2. Pyogenic bacteria
streptococcus pneumonia, streptococcus mileri, staphylococcus
aureus, hemopillus, E.coli. Anaerobes: bacteroides spp
3. TB
Occurs due to complications of pulmonary TB through torn
subpleural foci or through lymph flow.
Pleura effusion
Pleura effusion
Additional Complaints: Diagnostic examination results:
● Inflammation can result in
● Cough friction rub
● Pleurisy pain ● bronchial breath sounds.
● Heavy feeling in the chest ● Focal fremitus weakens
● Weight loss ● On percussion, Ellis Damoiseu
● cyanosis was deaf.
Pleura effusion
Laboratory :

• Neutrophils increase
• The pleural puncture is cloudy,
yellowish/blood red in color
Pleura effusion
Xray :
● Pleura line +
● Compressive atelectasis (partial lung
collapse)

Laboratory :
• Neutrophils increase
• The pleural puncture is cloudy,
yellowish/blood red in color
Pleura effuson
INITIAL PROCEDURE
1. Thoracynthesis
a. To remove pleural fluid
b. Obtain specimens for analysis
c. Eliminates dyspnea

2. Insertion of a chest tube or drainage, this is done if thoracentesis


causes pain, protein and electrolyte depletion.

3. Medicines: Giving antibiotics if the causative agent is a germ or


bacteria.
Bronchodilator Pharmacology
• Beta 2 Agonist

Pharmacodynamics: Pharmacokinetics:

• Minimally absorbed from the


gastrointestinal tract
• Does not cross the blood-brain
barrier
• Extensively metabolized in the liver
to inactive metabolites
• Excreted rapidly in urine and feces
Bronchodilator Pharmacology
preparation :
Short Acting Long Acting
Bronchodilator Pharmacology
• Antikolinergik

Pharmacodynamics : Pharmacokinetic:
Cholinergic antagonists such as
ipratropium bromide are usually
administered by inhalation. This drug is
absorbed by the respiratory tract and
provides a long-lasting bronchodilation
effect. The duration of effect depends
on the dose and formulation of the
drug. Drug metabolism occurs primarily
in the liver, and the drug is excreted
primarily in the urine.
• Examples of drugs: Ipratropium
bromide, tiotropium bromide.
Bronchodilator Pharmacology
• Metilsaklin

Pharmacodynamics : Pharmacokinetic :
Methylxanthine, like theophylline, Methylxanthines such as theophylline
works as a bronchodilator by several can be given orally, intravenously, or in
mechanisms, including increasing the suppository form. After oral
activity of the adenylate cyclase administration, the drug is absorbed by
enzyme and inhibiting the the digestive tract and reaches the
phosphodiesterase enzyme. This lungs via the bloodstream. The half-life
causes relaxation of the smooth of the drug varies depending on the
muscles of the bronchi and blood dose and patient condition. Metabolism
vessels in the lungs, thereby expanding primarily occurs in the liver, and the
the airways and increasing air flow to drug is excreted primarily in the urine.
the lungs. Example of a drug: Theophylline.
Example of a drug: Theophylline.
Bronchodilator Pharmacology
• Adrenalin

Pharmacodynamics :
• For emergencies
• Subcutaneous injection dose of
0.01 mg/kgBB
• Rapid onset
• Works to reduce bronchospasm
and vasodilation
• Maximum dose 0.05 mg
Referance
1. Mosenifar Z. Chronic Obstructive Pulmonary Disease (COPD). Medscape.
2020. https://emedicine.medscape.com/article/297664-overview
2. Agarwal AK, Raja A, Brown BD. Chronic Obstructive Pulmonary Disease.
[Updated 2021 Dec 10]. In: StatPearls. Treasure Island (FL): StatPearls
Publishing; 2022 January
3. Paru, P., & Kronik, O. (2003). ( ppok ) 1973 - 2003. 1973–2003.
4. Hood Alsagaff,Abdul Mukty.2008.Dasar-dasar Ilmu Penyakit
Paru.Surabaya:Penerbit Erlangga
5. Jeremy P.T,dkk.2008. At a Glance SISTEM RESPIRASI.Jakarta: Penerbit
Erlangga
6. Perhimpunan Dokter Paru Indonesia. Pedoman Diagnosis dan Tatalaksana
Asma. 2021.
7. Soepandi PZ, Burhan E, Nawas A, Giriputro S, Isbaniyah F, Agustin H,
Handayani D. Pneumonia komunitas. Pedoman Diagnosis dan
Penatalaksanaan di Indonesia. Jakarta: Perhimpunan Dokter Paru
Indonesia; 2014.

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