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Infectious
disease….cont.
Prolonged
fever with
infectious
cause
Dr.Dhuha Sabeeh
Pediatric department
Prolonged fever?
 Defined as a duration of fever of 5 days or more
Infectious causes
 Abscess : intra-abdominal,
intracranial
 Wound infection ,OM
 Bacterial : Typhoid, brucella..
 Viral : EB,CMV,HIV
 TB
 Parasitic ,Malaria,leishmania
Non-Infectious causes
Causes of prolonged fever
At the end of lecture , will learn :
 Deferential diagnosis for prolonged fever
 Describe the etiology and its presentation
 Evaluation through history and examination
 Outline the management plan
Learning
objectives
Case scenario
 A 5-year-old child presented with fever since 8 days
associated with headache, malaise, diarrhea and skin
rash. her mother said that she is also had a history of
fever, constipation and malaise in last 2 weeks.
On examination : conscious , toxic appearing child ,HR: 64
b/m Temp. 39.5C. Abdominal examination reveal liver and
spleen palpable 2cm each.
Investigations: CBC : Hb 11g/dl,WBC 2500c/cmm,PLT
180.000c/cmm
Enteric Fever
Typhoid fever
 Is a systemic infectious disease caused by the gram-
negative bacillus Salmonella enterica serotype Typhi
and Paratyphi
Pathogenesis
 The organism enters the body
through the walls of the intestinal
tract and, following a transient
bacteremia, multiplies in the
reticuloendothelial cells of the
liver and spleen.
 Persistent bacteremia and
symptoms then follow.
 Bacterial emboli produce the
characteristic skin lesions (rose
spots)
1st week :
 A slow rising tempreture
 Relative bradycardia
 Malaise,aneroxia
 Headache
 Cough
 Abdominal pain ,vomiting,
diarrhea
2nd week :
 Continuing high fever
 Bradycardia continue
 Constipation
 Skin rash
 HSM
 Distended abd.
 Sometime agitated
3rd week :
 Anumber of
complications can occur
 GIT bleeding,perforation
 Encephalopathy
 Dehydration
 Shock,DIC
4th week :
Long recovery
peroid
Clinical manifestations
 Incubation period (7-14days)
 The classic lengthy three-stage disease seen in adult patients often is
shortened in children
Clinical manifestations
Rose spots
 The typical typhoidal rash (rose spots)
is present in 10%–15% of children. It
appears during the second week of the
disease
 Rose spots are erythematous
maculopapular lesions.
 They are found principally on the trunk
and chest and they generally disappear
within 3–4 days.
Laboratory Findings
 Typhoid bacilli can be
isolated from many sites,
including blood, stool,
urine, and bone marrow.
 Blood cultures are positive
in 50%–80% of cases
during the first week
 Stool cultures are positive
in about 50% of cases after
the first week.
Serologic tests (Widal reaction) are
not as useful as cultures because both
false-positive and false-negative results
occur. positive second week of illness.
PCR,EIA
CBC: Leukopenia is common,
thrombocytopenia is marker of severe
illness and DIC
Mild elevation of liver enzymes,
MCQ
A 7-year-old boy was admitted with a history of intermittent
high grade fever for 6 days , associated with vomiting,
myalgia, and headache. He had 3 days of loose green stools
followed by constipation. You suspected typhoid fever, the
MOST sensitive test for the diagnosis in this period of illness
is :
A. Blood culture
B. Complete blood picture
C. Stool culture
D. Urine culture
E. Widal test
Complications
The most serious complications of typhoid fever are
gastrointestinal hemorrhage and perforation. They occur toward
the end of the second week or during the third week of the disease
.The clinical manifestations are pain, tenderness, and rigidity in
the right lower quadrant.
An encephalopathy may be seen with irritability, confusion,
delirium, and stupor
Bacterial pneumonia, septic arthritis, abscesses, and
osteomyelitis,DIC are uncommon complications, particularly if
specific treatment is given promptly.
About 1%–3% of patients become chronic typhoid carriers
Treatment
 Third-generation cephalosporins
(e.g. Ceftriaxon 75mg/kg/d for 10-14 days)
 Azithromycin : 10-20 mg/kg /day for 7days
 Amoxicillin 75-100m/kg/day for 14 days
 Chloramphenicol
 Ciprofloxacin or other fluoroquinolones are used for multiply
resistant strains.
 Patients may remain febrile for 3–5 days even with appropriate
therapy.
General support of the
patient is important and
includes rest, good
nutrition and hydration,
and careful observation
Antimicrobial therapy
Case Scenario
 A 10-year-old male, presented with 2 weeks of fever, diarrhoea
and abdominal pain. Blood cultures grew Salmonella typhi, of
which he was commenced on intravenous Ceftriaxone 2 grams
twice daily. On day 3 of treatment, he developed acute
confusional state.
 What is the most likely diagnosis?
 What additional treatment he need ?
Steroid :
 Indicated only in shock, altered sensorium
 Dexamethasone in the dose of 3 mg/kg followed by 1
mg/kg every 6 hours for 2 days
typhoid encephalopathy
Case
Prevention
 Routine typhoid vaccine is not recommended
but should be considered when travel to
endemic areas.
 An attenuated oral typhoid vaccine has better
efficacy and causes minimal side effects.
 A capsular polysaccharide vaccine (ViCPS)
requires one intramuscular injection and may
be given to children age 2 years and older
Case scenario
 A 7-year-old boy presents with history of fever for one month
associated with periodic abdominal pain, weight loss, excessive
sweating and malaise. He received different antibiotics but no
response ,the symptoms persist with development of arthralgia.
The boy was well previously and he spent several weeks in his
grandfather farm ,where he liked to eat home-made diaries
 Physical examination reveal ill looking child ,pale ,Temp : 39C°
,HR 110 BPM , cervical lymphadenopathy . palpable
hepatosplenomegaly
Brucellosis is a zoonosis dz caused by infection with
the bacterial genus Brucella.
Brucellosis
Animal Reservoir
Organism
Goats, sheep, camels
B melitensis
Cows, buffalo, camels, yaks
B abortus
Pigs (biotype 1-3)
B suis
Canines
Brucella canis
Transmission
 Ingestion of unpasteurized milk and related dairy
products.
 Aerosolization of fluids, contamination of skin
abrasions, and splashing of mucous membranes
among workers , farmers and who is live there
 Incubation period is generally 2-4 wk
 Fever is the most common symptom which is associated with
chills and sweating
 Constitutional symptom: anorexia, fatigue, weakness, and
malaise
 Bone and joint symptoms include arthralgias, low back pain,
spine and joint pain, and, rarely, joint swelling.
 Hepatic and splenic enlargement
Clinical Manifestations
 CBC shows leukopenia, relative lymphocytosis or
pancytopenia.
 LFT shows slight elevation
 Blood culture has sensitivity of 60%
 Bone marrow culture has sensitivity of 80-90%.
Diagnosis
Serology:
 Serum agglutination test :titers of more than 1:160
 ELISA
 PCR
Management
 The World Health Organization recommends the following for
Children ≥ 8 yr:
 Doxycycline 4.4mg/kg bid and rifampin 15-20mg/kg PO: Both
drugs are to be given for 6 weeks
 Doxycycline 4.4mg/kg bid for 6 weeks and streptomycin 20-40
mg/kg IM daily for 2-3 weeks
 Gentamicin 6-7.5 mg/kg can be used as a substitute for
streptomycin and has shown equal efficacy.
Management
 Children < 8 years:
The use of rifampin and trimethoprim-sulfamethoxazole ( TMP
10mg/kg –SMX50 mg/kg) for 6 weeks is the therapy of choice.
 For complications:
 Meninigitis
 Osteomyelitis
 Spondylitis
 Endocarditis
Doxycycline + Gentamicin+ rifampin
MCQ
 An 11-year-old child who was admitted to the hospital due to
fever for 15 days associated with abdominal pain .On abdominal
ultrasound, she had hepato-splenomegaly .diagnostic workup
for infectious disorders confirmed brucellosis. What is the
proper choice of therapy ?
A. Rifampin and trimethoprim-sulfamethoxazole
B. Third generation cephalosporine
C. Doxycycline and rifampin
D. Doxycycline + Gentamicin+ rifampin
E. Rifampin and streptomycin
 Effective eradication of the organism from cattle,
goats, as well as from other animals.
 Pasteurization of milk and dairy products for
human consumption
 No vaccine
Prevention
Case scenario
18-months-old girl referred from border-hospital with
three weeks history of high grade intermittent fever
associated with poor feeding ,diarrhea and weight loss.
On examination cachexia child , pale and icterus ,Temp.
39.2°C, spleen were palpable 8cm ,liver 4cm
Laboratory tests show (WBC 2000 c/cmm, Hb 5.3 g/dl, PLT
50.000 c /cmm)
What is the most likely diagnosis?
Leshmaniasis
• The leishmaniases are a group of parasitic diseases caused by
protozoa of the Leishmania genus and transmitted by the bites
of phlebotomine sandfly species
 Multiple species of Leishmania are known to cause human
disease involving the skin and mucosal surfaces
Localized cutaneous leishmaniasis (LCL) Diffuse cutaneous leishmaniasis
Leshmaniasis presentation
Mucosal leishmaniasis (ML)
Leshmaniasis
Visceral leishmaniasis
Visceral leishmaniasis
(VL)(kala-azar)
• Visceral leishmaniasis (VL), also known as kala-azar,
is the most severe form of leishmaniasis caused by
L.donovani and L. infantum
• Typically affects children <5 yr
Classic clinical features of Kala azar
 High fever (prolonged)
 Marked splenomegaly
 Hepatomegaly
At terminal stages of kala-azar
Massive HSM
Gross wasting(malnutrition)
Jaundice ,edema, and ascites
Severe anemia enough to precipitate HF
Bleeding episodes
 The late stage of the illness
 is often complicated by secondary bacterial infections, which
Laboratory finding
 Patients with cutaneous LCL or ML generally do not have
abnormal laboratory results unless the lesions are
secondarily infected with bacteria.
 Laboratory findings associated with classic kala azar
include :
 CBC :anemia ,thrombocytopenia, leukopenia
(pancytopenia)
 Elevated hepatic transaminase levels
 Hyperglobulinemia
Diagnosis
 Find amastigotes in:
LCL,ML is diagnosed by making the smear from
the deeper area of the skin lesion.
 VL is diagnosed through:
• Bone marrow aspirate reveal LD bodies
 ELIZA and indirect fluorescent antibody assay
Diagnosis
 Specific
 Sodium stibogluconate (antimony sodium
gluconate (Pentostam).
 Recommended regimen is 20 mg/kg/day
intravenously or intramuscularly for 20 days (for
LCL and DCL) and 28 days (for ML and VL)
Treatment
Side effects
 Are dose and duration dependent
 Elevated hepatic transaminase level ,elevated
amylase and lipase levels ,
 Mild hematologic changes (slightly decreased
leukocyte count, hemoglobin level, and platelet
count)
 Nonspecific T-wave, cardiac toxicity(rare)
Other (alternative)
 Amphotericin B desoxycholate (SE.renal toxicity )
 Liposomal amphotericin B
 Aminoglycoside paromomycin
 Miltefosine
 Fluconazole
 Blood and platelet transfusion if indicated
 Antibiotic for secondary bacterial infection
 Rehabilitation for malnutrition
 Antipyretic as required
 Prevention
Control & elimination of the infected reservoir hosts
Early recognition and treatment of the case.
Supportive therapy
References
 Nelson Textbook of Pediatrics
 Nelson essentials Textbook of Pediatrics
 Illustrated textbook of pediatrics

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L1 prolong fever PPT for pediatrics.pptx

  • 2. Prolonged fever?  Defined as a duration of fever of 5 days or more
  • 3. Infectious causes  Abscess : intra-abdominal, intracranial  Wound infection ,OM  Bacterial : Typhoid, brucella..  Viral : EB,CMV,HIV  TB  Parasitic ,Malaria,leishmania Non-Infectious causes Causes of prolonged fever
  • 4. At the end of lecture , will learn :  Deferential diagnosis for prolonged fever  Describe the etiology and its presentation  Evaluation through history and examination  Outline the management plan Learning objectives
  • 5. Case scenario  A 5-year-old child presented with fever since 8 days associated with headache, malaise, diarrhea and skin rash. her mother said that she is also had a history of fever, constipation and malaise in last 2 weeks. On examination : conscious , toxic appearing child ,HR: 64 b/m Temp. 39.5C. Abdominal examination reveal liver and spleen palpable 2cm each. Investigations: CBC : Hb 11g/dl,WBC 2500c/cmm,PLT 180.000c/cmm
  • 6. Enteric Fever Typhoid fever  Is a systemic infectious disease caused by the gram- negative bacillus Salmonella enterica serotype Typhi and Paratyphi
  • 7. Pathogenesis  The organism enters the body through the walls of the intestinal tract and, following a transient bacteremia, multiplies in the reticuloendothelial cells of the liver and spleen.  Persistent bacteremia and symptoms then follow.  Bacterial emboli produce the characteristic skin lesions (rose spots)
  • 8. 1st week :  A slow rising tempreture  Relative bradycardia  Malaise,aneroxia  Headache  Cough  Abdominal pain ,vomiting, diarrhea 2nd week :  Continuing high fever  Bradycardia continue  Constipation  Skin rash  HSM  Distended abd.  Sometime agitated 3rd week :  Anumber of complications can occur  GIT bleeding,perforation  Encephalopathy  Dehydration  Shock,DIC 4th week : Long recovery peroid Clinical manifestations  Incubation period (7-14days)  The classic lengthy three-stage disease seen in adult patients often is shortened in children
  • 10. Rose spots  The typical typhoidal rash (rose spots) is present in 10%–15% of children. It appears during the second week of the disease  Rose spots are erythematous maculopapular lesions.  They are found principally on the trunk and chest and they generally disappear within 3–4 days.
  • 11. Laboratory Findings  Typhoid bacilli can be isolated from many sites, including blood, stool, urine, and bone marrow.  Blood cultures are positive in 50%–80% of cases during the first week  Stool cultures are positive in about 50% of cases after the first week. Serologic tests (Widal reaction) are not as useful as cultures because both false-positive and false-negative results occur. positive second week of illness. PCR,EIA CBC: Leukopenia is common, thrombocytopenia is marker of severe illness and DIC Mild elevation of liver enzymes,
  • 12. MCQ A 7-year-old boy was admitted with a history of intermittent high grade fever for 6 days , associated with vomiting, myalgia, and headache. He had 3 days of loose green stools followed by constipation. You suspected typhoid fever, the MOST sensitive test for the diagnosis in this period of illness is : A. Blood culture B. Complete blood picture C. Stool culture D. Urine culture E. Widal test
  • 13. Complications The most serious complications of typhoid fever are gastrointestinal hemorrhage and perforation. They occur toward the end of the second week or during the third week of the disease .The clinical manifestations are pain, tenderness, and rigidity in the right lower quadrant. An encephalopathy may be seen with irritability, confusion, delirium, and stupor Bacterial pneumonia, septic arthritis, abscesses, and osteomyelitis,DIC are uncommon complications, particularly if specific treatment is given promptly. About 1%–3% of patients become chronic typhoid carriers
  • 14. Treatment  Third-generation cephalosporins (e.g. Ceftriaxon 75mg/kg/d for 10-14 days)  Azithromycin : 10-20 mg/kg /day for 7days  Amoxicillin 75-100m/kg/day for 14 days  Chloramphenicol  Ciprofloxacin or other fluoroquinolones are used for multiply resistant strains.  Patients may remain febrile for 3–5 days even with appropriate therapy. General support of the patient is important and includes rest, good nutrition and hydration, and careful observation Antimicrobial therapy
  • 15. Case Scenario  A 10-year-old male, presented with 2 weeks of fever, diarrhoea and abdominal pain. Blood cultures grew Salmonella typhi, of which he was commenced on intravenous Ceftriaxone 2 grams twice daily. On day 3 of treatment, he developed acute confusional state.  What is the most likely diagnosis?  What additional treatment he need ? Steroid :  Indicated only in shock, altered sensorium  Dexamethasone in the dose of 3 mg/kg followed by 1 mg/kg every 6 hours for 2 days typhoid encephalopathy Case
  • 16. Prevention  Routine typhoid vaccine is not recommended but should be considered when travel to endemic areas.  An attenuated oral typhoid vaccine has better efficacy and causes minimal side effects.  A capsular polysaccharide vaccine (ViCPS) requires one intramuscular injection and may be given to children age 2 years and older
  • 17. Case scenario  A 7-year-old boy presents with history of fever for one month associated with periodic abdominal pain, weight loss, excessive sweating and malaise. He received different antibiotics but no response ,the symptoms persist with development of arthralgia. The boy was well previously and he spent several weeks in his grandfather farm ,where he liked to eat home-made diaries  Physical examination reveal ill looking child ,pale ,Temp : 39C° ,HR 110 BPM , cervical lymphadenopathy . palpable hepatosplenomegaly
  • 18. Brucellosis is a zoonosis dz caused by infection with the bacterial genus Brucella. Brucellosis Animal Reservoir Organism Goats, sheep, camels B melitensis Cows, buffalo, camels, yaks B abortus Pigs (biotype 1-3) B suis Canines Brucella canis
  • 19. Transmission  Ingestion of unpasteurized milk and related dairy products.  Aerosolization of fluids, contamination of skin abrasions, and splashing of mucous membranes among workers , farmers and who is live there
  • 20.  Incubation period is generally 2-4 wk  Fever is the most common symptom which is associated with chills and sweating  Constitutional symptom: anorexia, fatigue, weakness, and malaise  Bone and joint symptoms include arthralgias, low back pain, spine and joint pain, and, rarely, joint swelling.  Hepatic and splenic enlargement Clinical Manifestations
  • 21.  CBC shows leukopenia, relative lymphocytosis or pancytopenia.  LFT shows slight elevation  Blood culture has sensitivity of 60%  Bone marrow culture has sensitivity of 80-90%. Diagnosis Serology:  Serum agglutination test :titers of more than 1:160  ELISA  PCR
  • 22. Management  The World Health Organization recommends the following for Children ≥ 8 yr:  Doxycycline 4.4mg/kg bid and rifampin 15-20mg/kg PO: Both drugs are to be given for 6 weeks  Doxycycline 4.4mg/kg bid for 6 weeks and streptomycin 20-40 mg/kg IM daily for 2-3 weeks  Gentamicin 6-7.5 mg/kg can be used as a substitute for streptomycin and has shown equal efficacy.
  • 23. Management  Children < 8 years: The use of rifampin and trimethoprim-sulfamethoxazole ( TMP 10mg/kg –SMX50 mg/kg) for 6 weeks is the therapy of choice.  For complications:  Meninigitis  Osteomyelitis  Spondylitis  Endocarditis Doxycycline + Gentamicin+ rifampin
  • 24. MCQ  An 11-year-old child who was admitted to the hospital due to fever for 15 days associated with abdominal pain .On abdominal ultrasound, she had hepato-splenomegaly .diagnostic workup for infectious disorders confirmed brucellosis. What is the proper choice of therapy ? A. Rifampin and trimethoprim-sulfamethoxazole B. Third generation cephalosporine C. Doxycycline and rifampin D. Doxycycline + Gentamicin+ rifampin E. Rifampin and streptomycin
  • 25.  Effective eradication of the organism from cattle, goats, as well as from other animals.  Pasteurization of milk and dairy products for human consumption  No vaccine Prevention
  • 26. Case scenario 18-months-old girl referred from border-hospital with three weeks history of high grade intermittent fever associated with poor feeding ,diarrhea and weight loss. On examination cachexia child , pale and icterus ,Temp. 39.2°C, spleen were palpable 8cm ,liver 4cm Laboratory tests show (WBC 2000 c/cmm, Hb 5.3 g/dl, PLT 50.000 c /cmm) What is the most likely diagnosis?
  • 27. Leshmaniasis • The leishmaniases are a group of parasitic diseases caused by protozoa of the Leishmania genus and transmitted by the bites of phlebotomine sandfly species
  • 28.  Multiple species of Leishmania are known to cause human disease involving the skin and mucosal surfaces Localized cutaneous leishmaniasis (LCL) Diffuse cutaneous leishmaniasis Leshmaniasis presentation
  • 30. Visceral leishmaniasis (VL)(kala-azar) • Visceral leishmaniasis (VL), also known as kala-azar, is the most severe form of leishmaniasis caused by L.donovani and L. infantum • Typically affects children <5 yr
  • 31. Classic clinical features of Kala azar  High fever (prolonged)  Marked splenomegaly  Hepatomegaly At terminal stages of kala-azar Massive HSM Gross wasting(malnutrition) Jaundice ,edema, and ascites Severe anemia enough to precipitate HF Bleeding episodes  The late stage of the illness  is often complicated by secondary bacterial infections, which
  • 32. Laboratory finding  Patients with cutaneous LCL or ML generally do not have abnormal laboratory results unless the lesions are secondarily infected with bacteria.  Laboratory findings associated with classic kala azar include :  CBC :anemia ,thrombocytopenia, leukopenia (pancytopenia)  Elevated hepatic transaminase levels  Hyperglobulinemia Diagnosis
  • 33.  Find amastigotes in: LCL,ML is diagnosed by making the smear from the deeper area of the skin lesion.  VL is diagnosed through: • Bone marrow aspirate reveal LD bodies  ELIZA and indirect fluorescent antibody assay Diagnosis
  • 34.
  • 35.  Specific  Sodium stibogluconate (antimony sodium gluconate (Pentostam).  Recommended regimen is 20 mg/kg/day intravenously or intramuscularly for 20 days (for LCL and DCL) and 28 days (for ML and VL) Treatment
  • 36. Side effects  Are dose and duration dependent  Elevated hepatic transaminase level ,elevated amylase and lipase levels ,  Mild hematologic changes (slightly decreased leukocyte count, hemoglobin level, and platelet count)  Nonspecific T-wave, cardiac toxicity(rare)
  • 37. Other (alternative)  Amphotericin B desoxycholate (SE.renal toxicity )  Liposomal amphotericin B  Aminoglycoside paromomycin  Miltefosine  Fluconazole
  • 38.  Blood and platelet transfusion if indicated  Antibiotic for secondary bacterial infection  Rehabilitation for malnutrition  Antipyretic as required  Prevention Control & elimination of the infected reservoir hosts Early recognition and treatment of the case. Supportive therapy
  • 39. References  Nelson Textbook of Pediatrics  Nelson essentials Textbook of Pediatrics  Illustrated textbook of pediatrics