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Seminar presentation on
pneumonia
Presented by
ferhan mahamud
felmata abdi
hanan muktar
endisar abdela
Out line
• Introduction
• epidemiology
• pathophysiology
• etiology
• Classification and risk factors
• clinical manifestations
• Laboratory and other investigations
• Treatment
Introduction
•Pneumonia:
• is acute infection and inflammation
of the lung tissue caused by various
bacterial species, viruses, fungi or
parasites.
Epidemiology
• Pneumonia remains:
• one of the most common causes of severe sepsis and
• leading infectious cause of death in children and
adults
• a mortality rate as high as 50% depending on the
severity of illness
• It occurs in persons of all ages, although the clinical
manifestations are most severe in the very young,
and elderly,
Etiology
• lung Infections( by impairing alveormacrophage and
mucociliary clearance)
• Aspiration of gastric contents
• Malnutrition, lack of immunization
•
• • Rickets, preceding upper respiratory tract infection
•
• • Exposure to cigarette smokes, indoor air pollution
•
• • Immunosuppression ( HIV, cancer, alcohol dependence,)
•Any alteration of the normal lung microbiome by infection or.
disease can lead to pneumonia
Causative pathogen vary according to
age and patient conditions
• Neonates: group B streptococcus, Klebsiella, E.coli,
Chlamydia and S. aureus
•
• • Children <5 years: streptococcus pneumonia
. - (Pneumococcus), Haemophilus
influenzae,
• less frequently: S. aureus, M. Pneumoniae, viruses (
influenza, measles)
•
• • Children and adult >5 years: most commonly
S.pneumoniae, followed by atypical bacteria, e.g.
• Pneumonia in pt with cytic fibrosis is caused by
- S. aureus in infancy and p. aeruginosa •
, in older pt.
• Pneumonia in immunocompromised child is
caused by : pneumocystis ( in HIV infected)
Pathophysiology
• Pneumonia results from the proliferation of microbial
pathogens at the alveolar level and the host's
response to those pathogens
• Respiratory pathogens enter the lower respiratory
• tract by one of three routes:
• 1) direct inhalation of infectious droplets
• 2) aspiration of oropharyngeal contents or
• 3) hematogenous spread from another infection site
Classification of pneumonia
• According to environment :
1) CAP : pneumonia developing outside the
hospital or <48 hour after hospital
admission
risk factor : DM,asplenia, pulmonary disease
2) HAP : pneumonia developing >48 hours
after hospital admission
risk factor : witnessed aspiration, COPD , MDR risk such as
MRSA and MDR pseudomonas if IV antibiotic use within 90
days
3) VAP : pneumonia developing >48 hours
after endotracheal intubation
risk factor: acute replacement therapy preceding VAP or
5+ day of hospitalization preceding VAP
• 2) According to the causative
organisms
• a, Bacterial
b, virus
c, parasite
d, fungal
Virus
Parasite : ascaris and strongloides species
3) According to Infection
There are two major types:
• Bronchopneumonia: involves both the lung
parenchyma and the bronchi.
It is common in children and the elderly.
• Lobar pneumonia: involves one or more lobes
of the lung. It is common in young people
Clinical manifestations
• Pneumonia:
• • Cough
• • Fast breathing
• • But no signs for severe pneumonia
• Severe pneumonia:
•Cough or difficult breathing
•Lower chest indrawing,
•Nasal flaring,
•Grunting in young infants.
•Fast breathing( 2 -12 month : >/ =50 bpm, 1-5yr >/=
40bpm
• abnormal breath sounds may. also be present
Clinical manifestations of
atypical pneumonia
• − Fever, Tiredness (fatigue), headache
•
• − Skin rash, ( malaise) general feeling of sickness
•
• − Cough, dry to phlegmy ear infections
•
• − sinus infection, sore throat
•
• − Wheezing in children who have an airway problem
such as asthma
Lab and other investigations
• The decision to treat a child who has pneumonia is usually
made clinically
•
• • Chest X ray and for looking complications,
Eg. Dense lobar or segmented infiltrates
• Sputum: For Gram stain, Ziehl-Neelsen (ZN) stain, ..
culture for AFB
•
• • Blood: Complete blood count
• Leukocytes with predominance of polymorphonuuclear cell
•
Treatment Approach of
pneumonia
• Gaol of treatment
Primary goals are
Eradication of the offending organism and
subsequent complete clinical cure
secondary goals are
minimization of the unintended consequence
Of therapy and
minimizing costs through outpatient and oral therapy
when the patient’s severity of illness and clinical
considerations permit
Non pharmacological treatment
• Frequent monitoring of all the vital signs in order
to detect complications early and to monitor
response to therapy, for all patients.
• Give attention to fluid and nutritional
replacements as required.
• Administer Oxygen via nasal
Treatment Of pneumonia
• Severe Pneumonia in an Infant (up
to 2 months):
•
Ampicilin is 50mg/kg IV
BID for neonates<14days old
, QID for those > 14 days,
In severely ill infants Ceftriaxone 100 mg/kg IV once
daily
Continue treatment for at least 7 days
Management of infant (up to 2month
• Admit, keep baby warm
•
• • Prevent hypo glycaemia by breastfeeding/giving
expressed breast milk/NGT
•
• • If child is lethargic, do not give oral feeds. Use IV.
fluids with care
•
• • Give oxygen to keep SpO2 >94%
Pneumonia in a child of 2 month-5yr
For non sever
_First-line
Amoxicillin, 25 mg/kg every 12hourss P.O for 5 days
- Alternatives
Azithromycin, 10mg/kg/24 P.O., once daily for 3
days mainly when patients have afebrile
pneumonia syndrome.
- Reassess child for progress after 3 days
Pneumonia in child of 2 Month-5year
for sever
Antipyretic : Paracetamol, 10-15mg /kg P.O., up to. . .
4-6 times a day for the relief of high fever
Alternatives: Ibuprofen, 5 – 10mg/kg/dose every 6 – .
8hr P.O. (max. 40mg/kg/24hours
• first-line
Benzyl penicillin, 50,000units/kg/24hours IV QID for at least 3 days
N.B. When the child improves switch to oral
Amoxicillin: 25 mg/kg/24 hours 3 times a day.
The total course of treatment is 5-7day
• If the child doesn’t improve within 48 hours, switch to
ceftriaxone 80mg/Kg/24 hours IM/IV BID for 5 days
• If staphylococcus is suspected (empyema
pneumatocele at X ray),
give gentamicin 5 mg/kg once daily plus
Cloxacillin 50 mg/kg IV every 6-hour
•
• Zinc supplementation in children <5years with severe
peumonia
For atypical pneumonia
Azithromycin, 10mg/kg P.O., on day 1, 5mg/kg on
day 2-5,
• for children <6 months of age
10mg/kg/day for 5 days
Treatment for HAP and VAP
• Patients at lower risk of drug resistant
organisms, ie those with:
No IV antibiotics within previous 3 months,
no structural lung damage( COPD,lung fibrosis),
few or no co-morbidities, and
Not known MRSA carriers
− Ceftazidime 75 mg/kg/day IV
( into 2 divided doses per day) AND Gentamicin 3 –
5 mg/kg/day IV (given once daily) for 7 days
• Patients at higher risk of drug resistant
organisms, ie those with:
history of IV antibiotic use within previous 3 months,
structural lung damage (Bronchiectasis, COPD,lung
fibrosis),
prior co-morbidities and known MRSA carrier
•
• − Piperacillin-Tazobactam 100 mg/kg IV q 8 hours for
7 day
Aspiration pneumonia
• Non-pharmacologic
•
• Give oxygen if SpO2 < 90% with nasal prongs and
• monitor through pulse oximetry for those in respiratory
distress via nasal cannula
• Gentle suction of thick secretions from upper airway
•
• Pharmacologic
•
• - Ceftriaxone 80mg/Kg/24 hours IM/IV + Metrondazole
7.5mg/kg every 8 hours
• - Refer the patient for possible removal
Management for complication
• Pleural effusion and empyema:
_Non-pharmacologic : Chest tubes (tube thoracostomy)
Insert chest tubes immediately after a complicated
parapneumonic pleural effusion or empyema thoracis is diagnosed.
• The key to resolution involves prompt drainage of
pleural fluid because delay leads to the formation of loculated
pleural fluid.
treat with : macrolide( azithromycin) plus ceftriaxon
Common side effect of
Medication
• Aminoglycoside (gentamicin):
- nephrotoxicity
- ototoxicity
• Cephalosporins(ceftriaxon,ceftazidin, cefepime):
- Hypersensitivity ,
- Diarrhoea and Pain at injection site
• penicillin ( ampiciline,amoxicillin) :
Hypersensitivity
•vancomycin: Redman syndrome, nephrotoxicity and
Hypotension and fever
Evaluation of Therapeutic Outcomes
• Progress should be noted in the first 2 days and
progression to complete resolution whithin 5 to 7
days
•Serum procalcitonin concentrations in combination
with clinical response criteria can be used in the
decision to discontinue antibiotic therapy
Patient education
• Limite Infection spread by :
- covering mouth , nose when coughing and sneezes
- wearing mask in public
- whashing hand frequently
• to complete the prescribed antibiotic course
• to drink plenty of water to liquefy and mobilize secretion
• educate about vaccination such as
- Polyvalent polysaccharide vaccines for prevent two of the
leading causes of bacterial pneumonia,
S.pneumoniae and
H. influenzae type b
Reference
• STG for general hospital in Ethiopia 4th
edition 2020
• Nelson textbook of pediatric 21 edition

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Presentation(1) of pneumonia last.pptx

  • 1. Seminar presentation on pneumonia Presented by ferhan mahamud felmata abdi hanan muktar endisar abdela
  • 2. Out line • Introduction • epidemiology • pathophysiology • etiology • Classification and risk factors • clinical manifestations • Laboratory and other investigations • Treatment
  • 3. Introduction •Pneumonia: • is acute infection and inflammation of the lung tissue caused by various bacterial species, viruses, fungi or parasites.
  • 4. Epidemiology • Pneumonia remains: • one of the most common causes of severe sepsis and • leading infectious cause of death in children and adults • a mortality rate as high as 50% depending on the severity of illness • It occurs in persons of all ages, although the clinical manifestations are most severe in the very young, and elderly,
  • 5. Etiology • lung Infections( by impairing alveormacrophage and mucociliary clearance) • Aspiration of gastric contents • Malnutrition, lack of immunization • • • Rickets, preceding upper respiratory tract infection • • • Exposure to cigarette smokes, indoor air pollution • • • Immunosuppression ( HIV, cancer, alcohol dependence,) •Any alteration of the normal lung microbiome by infection or. disease can lead to pneumonia
  • 6. Causative pathogen vary according to age and patient conditions • Neonates: group B streptococcus, Klebsiella, E.coli, Chlamydia and S. aureus • • • Children <5 years: streptococcus pneumonia . - (Pneumococcus), Haemophilus influenzae, • less frequently: S. aureus, M. Pneumoniae, viruses ( influenza, measles) • • • Children and adult >5 years: most commonly S.pneumoniae, followed by atypical bacteria, e.g.
  • 7. • Pneumonia in pt with cytic fibrosis is caused by - S. aureus in infancy and p. aeruginosa • , in older pt. • Pneumonia in immunocompromised child is caused by : pneumocystis ( in HIV infected)
  • 8. Pathophysiology • Pneumonia results from the proliferation of microbial pathogens at the alveolar level and the host's response to those pathogens • Respiratory pathogens enter the lower respiratory • tract by one of three routes: • 1) direct inhalation of infectious droplets • 2) aspiration of oropharyngeal contents or • 3) hematogenous spread from another infection site
  • 9. Classification of pneumonia • According to environment : 1) CAP : pneumonia developing outside the hospital or <48 hour after hospital admission risk factor : DM,asplenia, pulmonary disease 2) HAP : pneumonia developing >48 hours after hospital admission risk factor : witnessed aspiration, COPD , MDR risk such as MRSA and MDR pseudomonas if IV antibiotic use within 90 days 3) VAP : pneumonia developing >48 hours after endotracheal intubation risk factor: acute replacement therapy preceding VAP or 5+ day of hospitalization preceding VAP
  • 10. • 2) According to the causative organisms • a, Bacterial b, virus c, parasite d, fungal
  • 11.
  • 12. Virus
  • 13. Parasite : ascaris and strongloides species
  • 14. 3) According to Infection There are two major types: • Bronchopneumonia: involves both the lung parenchyma and the bronchi. It is common in children and the elderly. • Lobar pneumonia: involves one or more lobes of the lung. It is common in young people
  • 15. Clinical manifestations • Pneumonia: • • Cough • • Fast breathing • • But no signs for severe pneumonia • Severe pneumonia: •Cough or difficult breathing •Lower chest indrawing, •Nasal flaring, •Grunting in young infants. •Fast breathing( 2 -12 month : >/ =50 bpm, 1-5yr >/= 40bpm • abnormal breath sounds may. also be present
  • 16. Clinical manifestations of atypical pneumonia • − Fever, Tiredness (fatigue), headache • • − Skin rash, ( malaise) general feeling of sickness • • − Cough, dry to phlegmy ear infections • • − sinus infection, sore throat • • − Wheezing in children who have an airway problem such as asthma
  • 17. Lab and other investigations • The decision to treat a child who has pneumonia is usually made clinically • • • Chest X ray and for looking complications, Eg. Dense lobar or segmented infiltrates • Sputum: For Gram stain, Ziehl-Neelsen (ZN) stain, .. culture for AFB • • • Blood: Complete blood count • Leukocytes with predominance of polymorphonuuclear cell •
  • 18. Treatment Approach of pneumonia • Gaol of treatment Primary goals are Eradication of the offending organism and subsequent complete clinical cure secondary goals are minimization of the unintended consequence Of therapy and minimizing costs through outpatient and oral therapy when the patient’s severity of illness and clinical considerations permit
  • 19. Non pharmacological treatment • Frequent monitoring of all the vital signs in order to detect complications early and to monitor response to therapy, for all patients. • Give attention to fluid and nutritional replacements as required. • Administer Oxygen via nasal
  • 20. Treatment Of pneumonia • Severe Pneumonia in an Infant (up to 2 months): • Ampicilin is 50mg/kg IV BID for neonates<14days old , QID for those > 14 days, In severely ill infants Ceftriaxone 100 mg/kg IV once daily Continue treatment for at least 7 days
  • 21. Management of infant (up to 2month • Admit, keep baby warm • • • Prevent hypo glycaemia by breastfeeding/giving expressed breast milk/NGT • • • If child is lethargic, do not give oral feeds. Use IV. fluids with care • • • Give oxygen to keep SpO2 >94%
  • 22. Pneumonia in a child of 2 month-5yr For non sever _First-line Amoxicillin, 25 mg/kg every 12hourss P.O for 5 days - Alternatives Azithromycin, 10mg/kg/24 P.O., once daily for 3 days mainly when patients have afebrile pneumonia syndrome. - Reassess child for progress after 3 days
  • 23. Pneumonia in child of 2 Month-5year for sever Antipyretic : Paracetamol, 10-15mg /kg P.O., up to. . . 4-6 times a day for the relief of high fever Alternatives: Ibuprofen, 5 – 10mg/kg/dose every 6 – . 8hr P.O. (max. 40mg/kg/24hours • first-line Benzyl penicillin, 50,000units/kg/24hours IV QID for at least 3 days N.B. When the child improves switch to oral Amoxicillin: 25 mg/kg/24 hours 3 times a day. The total course of treatment is 5-7day
  • 24. • If the child doesn’t improve within 48 hours, switch to ceftriaxone 80mg/Kg/24 hours IM/IV BID for 5 days • If staphylococcus is suspected (empyema pneumatocele at X ray), give gentamicin 5 mg/kg once daily plus Cloxacillin 50 mg/kg IV every 6-hour • • Zinc supplementation in children <5years with severe peumonia
  • 25. For atypical pneumonia Azithromycin, 10mg/kg P.O., on day 1, 5mg/kg on day 2-5, • for children <6 months of age 10mg/kg/day for 5 days
  • 26. Treatment for HAP and VAP • Patients at lower risk of drug resistant organisms, ie those with: No IV antibiotics within previous 3 months, no structural lung damage( COPD,lung fibrosis), few or no co-morbidities, and Not known MRSA carriers − Ceftazidime 75 mg/kg/day IV ( into 2 divided doses per day) AND Gentamicin 3 – 5 mg/kg/day IV (given once daily) for 7 days
  • 27. • Patients at higher risk of drug resistant organisms, ie those with: history of IV antibiotic use within previous 3 months, structural lung damage (Bronchiectasis, COPD,lung fibrosis), prior co-morbidities and known MRSA carrier • • − Piperacillin-Tazobactam 100 mg/kg IV q 8 hours for 7 day
  • 28. Aspiration pneumonia • Non-pharmacologic • • Give oxygen if SpO2 < 90% with nasal prongs and • monitor through pulse oximetry for those in respiratory distress via nasal cannula • Gentle suction of thick secretions from upper airway • • Pharmacologic • • - Ceftriaxone 80mg/Kg/24 hours IM/IV + Metrondazole 7.5mg/kg every 8 hours • - Refer the patient for possible removal
  • 29. Management for complication • Pleural effusion and empyema: _Non-pharmacologic : Chest tubes (tube thoracostomy) Insert chest tubes immediately after a complicated parapneumonic pleural effusion or empyema thoracis is diagnosed. • The key to resolution involves prompt drainage of pleural fluid because delay leads to the formation of loculated pleural fluid. treat with : macrolide( azithromycin) plus ceftriaxon
  • 30. Common side effect of Medication • Aminoglycoside (gentamicin): - nephrotoxicity - ototoxicity • Cephalosporins(ceftriaxon,ceftazidin, cefepime): - Hypersensitivity , - Diarrhoea and Pain at injection site • penicillin ( ampiciline,amoxicillin) : Hypersensitivity •vancomycin: Redman syndrome, nephrotoxicity and Hypotension and fever
  • 31. Evaluation of Therapeutic Outcomes • Progress should be noted in the first 2 days and progression to complete resolution whithin 5 to 7 days •Serum procalcitonin concentrations in combination with clinical response criteria can be used in the decision to discontinue antibiotic therapy
  • 32. Patient education • Limite Infection spread by : - covering mouth , nose when coughing and sneezes - wearing mask in public - whashing hand frequently • to complete the prescribed antibiotic course • to drink plenty of water to liquefy and mobilize secretion • educate about vaccination such as - Polyvalent polysaccharide vaccines for prevent two of the leading causes of bacterial pneumonia, S.pneumoniae and H. influenzae type b
  • 33. Reference • STG for general hospital in Ethiopia 4th edition 2020 • Nelson textbook of pediatric 21 edition