DENGUEDENGUEHemorrhagic FeverHemorrhagic Fever
Grupo ni Louie
Introduction
Philippine Hemorrhagic fever was first reported in 1953. In 1958, hemorrhagic fever became a notifiable disease in the country and was later reclassified as Dengue Hemorrhagic fever.
Dengue cases usually peaks in the months of July to November and lowest during the month of February to April
Source of infection
Immediate source is a vector mosquito,the Aedes Aegypti or the common household mosquito.
The infected person
Etiologic AgentDengue virus types 1, 2, 3 and 4
Mode of Transmission
Mosquito bite (Aedes Aegypti)
Incubation Period
Uncertain, Probably 6 days to one week.
Period of CommunicabilityUnknown. Presumed to be on the first week
of illness when virus is still present in the blood.
SusceptibilityBoth sexes are equally
affected.
Both sexes are equally
affected. Peak age affected 5-9 years of age.
Peak age affected 5-9 years of age.
All person are
susceptible
All person are
susceptible
Age groups predominantly affected
are the preschool and school age.
Age groups predominantly affected
are the preschool and school age.
Occurrence is sporadic throughout the year. Epidemic usually occur during the rainy
season as June – November. Peak
months are September and October.
Susceptibility is universal. Acquired
immunity may be temporary but usually permanent.
Early Symptoms
FeverFever HeadacheHeadache
Muscle and joint achesMuscle and joint aches
MalaiseMalaiseDecrease appetiteDecrease appetite
VomitingVomiting
Restlessness followed by:Worsening of earlier
Symptoms
Petechiae Ecchymosis
Generalized rash
Acute phase symptoms include the following:
Shock-like state Sweaty (diaphoretic)
Cold, clammy extremities
Stages of Clinical Presentation
ToxicFebrile
Convalescent
Stages of Clinical Presentation
• First 4 days (DOH)
• Abrupt onset of high fever > 39-40 degrees
• Headache
• Malaise
• Nausea and Vomiting
• Muscle pain
Febrile
Stages of Clinical Presentation
• Flushing which may be accompanied by conjunctival infection and epistaxis may be observed at a later period
• Sometimes abdominal pain
Febrile
Hepatomegaly is commonly found and liver is usually soft and tender
Hepatomegaly is commonly found and liver is usually soft and tender
Stages of Clinical Presentation
Thrombocytopenia and rising hematocrit due to plasma leakage are usually detectable before the onset of Toxic stage
Thrombocytopenia and rising hematocrit due to plasma leakage are usually detectable before the onset of Toxic stage
Stages of Clinical Presentation
• 5-7th days• An abrupt fall to normal or
subnormal levels of temperature
• and varying degrees of circulatory disturbance will develop – (like unstable BP, narrow
pulse pressure and shock)
ToxicSevere abdominal pain, frequent bleeding from GI (hematemesis, melena may occur)
Severe abdominal pain, frequent bleeding from GI (hematemesis, melena may occur)
Stages of Clinical Presentation
• Recovery stage
• Appetite regained
• BP stable
• Generalize flushing
• “Herman’s sign”
Convalescent
The rash in dengue is called "Herman's rash". It appears on the upper and lower extremities, purplish or violaceous red with blanched areas about 1 cm or less in size.
The rash in dengue is called "Herman's rash". It appears on the upper and lower extremities, purplish or violaceous red with blanched areas about 1 cm or less in size.
Category I
Category II Category III Category IV
History or presence of fever 2-7 days duration, with a (+) tourniquet test or presence of skin flushing or petechial rash
Category I plus Presence of one or more Danger Signs (especially defervescence)
RestlessnessChanges in sensoriumCold, clammy skinSudden onset of
abdominal painDifficulty of breathingCircumoral cyanosisSeizuresSpontaneous bleeding
(gum bleeding, epistaxis, rashes, petechiae)
Category II plus Circulatory failure
Cold clammy skinWeak thready
pulseNarrow pulse
pressure ( less than 20mm/Hg)
HypotensionRestlessness
Category III plus profound shock with undetectable pulse and blood pressure
Categories of DHF
• Sustained high fever, lasting 2-7 days
• Hemorrhagic tendencies such as positive torniquet test, petechiae, epistaxis, bleeding GI tract, injection sites
• Thrombocytopenia ( < 100,000 platelets/mm3 )
• Evidence of plasma leakage
Clinical Diagnosis of DHF is base on four major characteristic manifestations
• Evidence of plasma leakage because of increased vascular permeability– Increase in hematocrit greater than 20% above
average for age, sex and population
– Pleural effusion, ascites and hypoproteinemia
– Decrease in hematocrit following volume replacement treatment greater than 20% of baseline
Clinical Diagnosis of DHF is base on four major characteristic manifestations
Pathophysiology
VasculopathyA positive tourniquet test indicating the increased capillary fragility is found in the early febrile stage. It may be a direct effect of dengue virus as it appears in the first few days of illness during the viremic phase.
Tourniquet test (capillary fragility test or Rumpel Leads test) a presumptive test which is positive in the presence of more than 20 petechiae within an inch square, after 5 minutes of test
Tourniquet test (capillary fragility test or Rumpel Leads test) a presumptive test which is positive in the presence of more than 20 petechiae within an inch square, after 5 minutes of test
Thrombocytopenia and platelet dysfunction.
Patients with DHF usually have platelet counts less than 100 x 109/L. Thrombocytopenia is most prominent during the toxic stage. The mechanisms of thrombocytopenia include decreased platelet production and increased peripheral destruction.
Platelet dysfunction PD as evidenced by the absence of adenosine diphosphate (ADP) release, was initially demonstrated in patients with DHF during the convalescent stage.
The platelet dysfunction might be the result of exhaustion from platelet activation triggered by immune complexes containing dengue antigen.
Coagulopathy – clotting disorder
During the acute febrile stage, mild prolongation of the prothrombin time and partial thromboplastin time, as well as reduced fibrinogen levels.
There are four distinct, but closely related, viruses that cause dengue DEN 1, DEN 2, DEN 3 and DEN 4.
Recovery from infection by one provides lifelong immunity
against that serotype but confers only partial and transient
protection against subsequent infection by the other three.
There is good evidence that sequential infection increases the risk of more serious disease resulting in DHF.
Medical Treatment• Symptomatic and supportive relief• Rapid replacement of Fluids (most
important treatment) like oresol and IV• Start IVF using D5LRS or D5 0.9NaCl or
plain LRS• Give fresh whole blood at 1-ml/KBW if
there is significant blood loss or if hematocrit continues to fall despite fluid resuscitation
Medical Treatment• Give fresh whole blood at 1-ml/KBW if
here is significant blood loss or if hematocrit continues to fall despite fluid resuscitation
• Give platelets when platelet count is below 150,000/uL or if there is significant blood loss and platelet count is below 150,000/uL, or there is continuous bleeding and hematocrit remains normal.
Outlook (Prognosis)
• With early and aggressive care, most patients recover from dengue hemorrhagic fever. However, half of untreated patients who go into shock do not survive
Comprehensive Health History• Patient X is 2 years and 9 months old a male toddler born and raised from South Cotabato • Informant: Patient’s mother• Reliability: 100%• Patient: Patient X• Birthday: November 10, 2005 Nationality : Filipino• Address: 271B, 61D, PA. South Cotabato
• Type of Admission: Direct from ER• Attending Physician: Dr. X• Final Diagnosis: Dengue Hemorrhagic Fever II• Ward: Pediatric Ward
• Hx: This is a case of a 3 year-old male with DHF II • Chief complaint: Fever• HPI: • 10 hours PTA - (+) high grade fever, vomiting for several hours•
Patient History• Patient X is a toddler, admitted into the hospital around 5:00 am carried by his mother. • He is born healthy, under normal spontaneous vaginal delivery without any body-marks or
observable congenital birth defects. He has completed his immunization program for the following vaccines: BCG, DPT, OPV, MEASLES and HEPA-B.
• Patient X being the youngest of three 3 siblings, stays with her mother most of time at home. This is his first time to contact a serious illness since his birth. Most of the time he frequently catch common colds and slight to moderate fever but not of a high grade fever. The night prior to his admission to the hospital, patient X is feverish and it worsens in the wee hours of the morning. Patient is irritable, crying and has vomited for about three times.
Physical AssessmentCATEGORY FINDINGS
General Appearance The patient looks weak and with eyebags.
Vital Signs Temperature: 40.5Respiration: 30 cpmPulse Rate: 110Blood Pressure: 90/40
Skin Upon inspection, the patient was noted to have flushed skin color
Hair The patient’s natural hair color is black. Soft and shiny.
Head/skull Upon inspection the skull is symmetrically aligned. No signs of lesions.
Eyes Eyes and eyebrows are symmetrically aligned with equal distribution of hair on both eyebrows.
PERRLA
Ears The color of both ears is the same with the facial skin and is symmetrically aligned. No ear discharge is noted.
Nose The external nose is symmetric and straight same color as with the facial skin. There is no nasal flaring. No obstruction in both nasal cavities
Lips Appears to be a little bit dry but not bluish or cyanotic. No lesions, cracks or warts are present
Neck The patient can move his head freely, no nodules palpated in the cervical area
Thorax/Lung Normal respiration, symmetrical chest expansion, clear breath sounds, negative retraction.
Heart/Cardiovascular Normal cardiac rate, symmetrical peripheral pulse noted.
Abdomen Normal bowel sound. Soft non tender abdomen
Muscoloskeletal Motor @ 4/5 upper and lower extremitiesBoth appear to be symmetric
Mental Status Conscious and oriented
Laboratory Exams Day 1 Day 3 Day 4 Normal Values
Hematology Resut
Hemoglobin 13.6 14.313.0 - 18.0 Cms
%
Hematocrit 0.41 0.43 0.40 - 0.54 Vol%
RBC 4.7 5 4.5 - 6.5x10 L
WBC 4.7 8.2 4.5 - 5.2x10 L
Segmenters 0.80 0.36 0.50 - 0.70
Lymphocytes 0.20 0.64 0.20 - 0.40
Platelet 138 190 150 - 350
Summary of Lab Results
Summary of Lab ResultsLaboratory Exams Day 1 Day 3 Day 4 Normal Values
Urinalysis
Physical Appearance
Colory Yellow Yellow
TransparencySlightly Hazy Clear
Reaction pH 6.0 4.6 - 8.0
Specific Gravity 1.03 1.010 - 1.035
Sugar Negative Absent
Protein Negative Absent
Microscopic
Pus Cell 0-3 Absent
RBC 0-1 0 - 5
Epithelial Cells Occasional
Protein Negative Absent
Crystal
Amorphous urates Positive
Amorphous Phosphate Blank
Summary of Lab Results
Laboratory Exams Day 1 Day 3 Day 4Normal
Values
Fecalysis
Color Yellow
Consistency Soft
Typhidot
IgG Positive
IgM Negative
Course in the ward Day 1In day 1, a 3-year old male patient carried by his mother was admitted with a chief complaint of fever. Ten hours prior to consultation, the patient had a high grade fever and vomiting for several hours according to the mother. The patient had a high grade fever of 40.5 0C and BP: 90/40. Diet as tolerated was ordered. Upon assessment the patient is positive for tonsillopharyngitis. . Anti-biotics was also part of his medication to treat his tonsilopharyngitis. Ampicillin testing was done and had negative result. At 1000H, patient had a febrile seizure with temperature 41.80C, Paracetamol was given. Stool examination was requested and the fecalysis result was normal, the stool was soft, yellow colored stool. At 0100H, the patient experienced chills with temperature of 38.80C. Paracetamol was given, patient’s temperature went down to 370C.
Course in the ward Day 2 & 3
In day 2, the patient is slightly febrile with temperature of 37.60C. The mother was instructed to continue TSB and increase fluid intake.
In day 3, the patient is still febrile, Paracetamol via IV was given. Doctor ordered for typhidot. The typhidot result were the following: IgG positive and IgM negative. The patient is negative on typhoid fever.
Course in the ward Day 4In day 4, a significant drop in his temperature was noted, as low as 36.8 oC which is a sign that the patient is entering into the toxic stage of Dengue Fever. This state of defervescence, is a period where the number of patient’s platelet is at its lowest. It is at this time where his attending physician ordered another Laboratory request for CBC and PC to check if Patient X’s platelet count is below the normal range of 150,000 to 350,000 /L, which is referred to as thrombocytopenia. Hemoglobin, hematocrit, RBC WBC and Platelet count are within normal limits. Segmenters are slightly decrease with the value of 0.36 which is below the normal value of 0.50-0.70. After the significant drop of the client’s temperature, Patient X temperature were elevated again for eight hours, a normal phenomenon for a DHF patient before entering into the convalescent stage. The patient had general rashes with itchiness.
Course in the ward Day 5 & 6
In day 5, the patient is afebrile and positive for Herman’s sign.
In day 6, the patient is afebrile and still positive for Herman’s sign. Additional medication was ordered Ascorbic acid with dosage of 100mg/5mL to be taken 1 tsp everyday. Diagnosis of Dengue Hemorrhagic Fever II was resolved. The patient was discharged.
Drug Study
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NCP
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