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๐ŸŒก๏ธ TROPICAL FEVER EMERGENCIES

COMPREHENSIVE DUAL-LEVEL CARE PROTOCOL


PRIMARY CARE → SECONDARY CARE
๐Ÿ“‹ For Doctors Only | Not for Public Use
Covers: Dengue | Malaria | Scrub Typhus | Leptospirosis | Enteric Fever (Typhoid)

๐Ÿฅ LEVEL OF CARE OVERVIEW

Procedure/Action Primary Care Secondary/Tertiary Care
Clinical recognition
โœ…
โœ…
Rapid diagnostic tests (RDT)
โœ…
โœ…
Oral rehydration / IV fluids
โœ…
โœ…
Oral antimalarials
โœ…
โœ…
IV Artesunate (severe malaria)
โš ๏ธ (if available)
โœ…
Empiric Doxycycline (Scrub Typhus)
โœ…
โœ…
IV Ceftriaxone
โœ…
โœ…
Blood transfusion
โŒ
โœ…
Platelet transfusion
โŒ
โœ…
Dialysis
โŒ
โœ…
Mechanical ventilation
โŒ
โœ…
ICU-level care
โŒ
โœ…

โฑ๏ธ CRITICAL TIME TARGETS

Milestone Target Time
Recognize warning signs
Immediate
Blood glucose check
≤ 5 min
IV access (if warning signs)
≤ 10 min
Rapid diagnostic tests
≤ 30 min
Start empiric antibiotics (if indicated)
≤ 1 hour
Start IV Artesunate (severe malaria)
Immediate
Transfer (if needed)
ASAP after stabilization

๐Ÿ“– OVERVIEW OF TROPICAL FEVERS IN INDIA

Seasonal Patterns

Disease Peak Season Region
Dengue
Monsoon & post-monsoon (July-November) Pan-India; urban > rural
Malaria
Monsoon & post-monsoon (June-October) Endemic: Odisha, Chhattisgarh, Jharkhand, NE states, MP, Maharashtra
Scrub Typhus
Post-monsoon (September-November) Hilly/forested: Himachal, Uttarakhand, NE states, South India
Leptospirosis
Monsoon & post-monsoon (July-November) Coastal: Kerala, Gujarat, Maharashtra, Andaman
Enteric Fever
Year-round; peaks in monsoon Pan-India; poor sanitation areas
Chikungunya
Monsoon & post-monsoon Pan-India (epidemic pattern)
Japanese Encephalitis
Monsoon (July-October) UP, Bihar, Assam, WB, Tamil Nadu (rice-growing)

Quick Comparison Table

Feature Dengue Malaria Scrub Typhus Leptospirosis Enteric Fever
Vector/Source
Aedes mosquito
Anopheles mosquito
Mite (chigger)
Contaminated water/soil
Fecal-oral
Incubation
4-7 days
7-30 days
6-21 days
5-14 days
7-21 days
Rash
Maculopapular (late)
โŒ Rare
โš ๏ธ(Variable) Maculopapular
โš ๏ธ Variable
Rose spots (rare)
Eschar
โŒ
โŒ
โœ… Pathognomonic
โŒ
โŒ
Hepatosplenomegaly
โš ๏ธVariable
โœ…
โš ๏ธ๏ธ (Variable)
โœ…
โœ…
Jaundice
โš ๏ธ(Variable) Rare
โœ… (severe)
โš ๏ธ(Variable)
โœ… Common
โš ๏ธ (Variable)Rare
Conjunctival suffusion
โŒ
โŒ
โŒ
โœ… Suggestive
โŒ
Platelet drop
โœ… Marked
โš ๏ธ (Variable)Mild-moderate
โš ๏ธ(Variable) Mild-moderate
โš ๏ธ (Variable)Mild
โš ๏ธ(Variable) Mild
ARDS/Pulmonary
โš ๏ธ(Variable)
โœ…
โœ… Common
โœ… Hemorrhage
โŒ Rare
Specific test
NS1, IgM
Smear, RDT
IgM ELISA
IgM ELISA, MAT
Blood culture

๐ŸŸข PART 1 โ€” PRIMARY CARE

Goal: Recognise → Identify Warning Signs → Start Treatment → Refer if Needed

1๏ธโƒฃ APPROACH TO ACUTE UNDIFFERENTIATED FEVER

Initial Assessment
Action Details
History
Duration, travel, occupation, animal contact, water exposure, sick contacts
Examine
Rash, eschar, jaundice, hepatosplenomegaly, lymphadenopathy, bleeding
Vitals
Temperature, BP, HR, RR, SpOโ‚‚
Warning signs
Check for each disease-specific warning sign
Blood glucose
Rule out hypoglycemia
Key History Questions
Question Significance
Duration of fever? < 7 days vs > 7 days
Travel to endemic area? Malaria, Scrub Typhus
Occupation? Farmer, sewage worker (Leptospirosis)
Wading through flood water? Leptospirosis
Animal contact? Leptospirosis
Bite/eschar noticed? Scrub Typhus
Unsafe water/food? Enteric fever
Mosquito exposure? Dengue, Malaria, Chikungunya
Similar illness in family/area? Epidemic (Dengue, Chikungunya)
Clinical Clues to Differentiate
Finding Suggests
Eschar (painless black scab)
Scrub Typhus
Conjunctival suffusion (redness without discharge)
Leptospirosis
Muscle tenderness (especially calf)
Leptospirosis
Relative bradycardia (HR not ↑ with fever)
Enteric Fever, Scrub Typhus
Severe thrombocytopenia (< 50,000)
Dengue
Splenomegaly prominent
Malaria, Enteric Fever
Altered sensorium + fever
Cerebral Malaria, Scrub Typhus, Leptospirosis
Jaundice + fever + renal failure
Leptospirosis, Severe Malaria
Pulmonary involvement (ARDS)
Scrub Typhus, Leptospirosis
Bleeding (petechiae, mucosal, GI)
Dengue

2๏ธโƒฃ RAPID DIAGNOSTIC TESTS AT PRIMARY CARE

Available Tests
Disease Rapid Test When Positive Sensitivity
Dengue
NS1 antigen
Day 1-5
80-90%
IgM antibody
Day 5+
90-95%
IgG antibody
Day 7+ (or secondary infection)
Variable
Malaria
RDT (Pf/Pv)
Any time during infection
90-95%
Peripheral smear
Any time
Gold standard
Scrub Typhus
IgM rapid test
Day 7+
Variable (60-90%)
Leptospirosis
IgM rapid test
Day 7+
Variable (50-80%)
Enteric Fever
Widal test
Day 7+
Poor specificity
Typhidot IgM
Day 4+
Moderate
Interpretation Notes
Test Note
Dengue NS1
Best in first 5 days; negative doesn't rule out
Dengue IgM
Becomes positive around day 5; use combo kit
Malaria RDT
Can remain positive after treatment; smear better for follow-up
Widal
Single titre unreliable; rising titre more useful; avoid if possible
Scrub Typhus IgM
May be negative early; treat empirically if clinical suspicion
๐Ÿ“Œ In endemic season with compatible syndrome, treat empirically โ€“ do not wait for test results

3๏ธโƒฃ DENGUE โ€“ PRIMARY CARE MANAGEMENT

Definition & Classification (WHO 2009)
Category Features
Dengue without Warning Signs
Fever + ≥ 2 of: nausea/vomiting, rash, aches, leukopenia, positive tourniquet test
Dengue with Warning Signs
Above + any warning sign (see below)
Severe Dengue
Severe plasma leakage, severe bleeding, or severe organ impairment
Warning Signs (MUST Recognize)
Warning Sign Indicates
Abdominal pain or tenderness
Plasma leakage
Persistent vomiting
Dehydration risk
Clinical fluid accumulation
Pleural effusion, ascites
Mucosal bleeding
Coagulopathy
Lethargy / Restlessness
Impending shock
Liver enlargement > 2 cm
Hepatic involvement
Laboratory: Hct increase with rapid platelet drop
Hemoconcentration
Phases of Dengue
Phase Day Features
Febrile
1-3
High fever, headache, myalgia, rash
Critical
4-6 (around defervescence)
โš ๏ธ Maximum risk of shock; plasma leakage
Recovery
7-10
Fluid reabsorption; risk of fluid overload
๐Ÿ“Œ Critical phase occurs when fever subsides โ€“ monitor closely during defervescence
Who Can Be Managed at Primary Care?
Can Manage Must Refer
Dengue without warning signs Any warning sign present
Tolerating oral fluids Severe dengue
Adequate urine output Bleeding
Stable vitals Shock / Hypotension
Hct stable Rising Hct with falling platelets
Platelets > 50,000 Platelets < 20,000
Fluid Management โ€“ Dengue WITHOUT Warning Signs
Patient Type Fluid
Tolerating orals
ORS, coconut water, fruit juices, rice kanji
Target 2-3 liters/day orally
Avoid NSAIDs (bleeding risk), Aspirin, IM injections
Paracetamol 500-1000 mg every 6 hrs (max 4 g/day)
Fluid Management โ€“ Dengue WITH Warning Signs
Step Action
1
Start IV crystalloid (NS or RL)
2
Initial bolus: 5-7 mL/kg/hr for 1-2 hours
3 If improving: Reduce to 3-5 mL/kg/hr for 2-4 hrs
4 If stable: Reduce to 2-3 mL/kg/hr
5 Monitor: Vitals hourly, Hct every 4-6 hrs
6
TRANSFER to higher centre
Fluid Calculation by Weight
Weight 5 mL/kg/hr 3 mL/kg/hr 2 mL/kg/hr
50 kg
250 mL/hr
150 mL/hr
100 mL/hr
60 kg
300 mL/hr
180 mL/hr
120 mL/hr
70 kg
350 mL/hr
210 mL/hr
140 mL/hr
80 kg
400 mL/hr
240 mL/hr
160 mL/hr
When to Suspect Dengue Shock
Sign
Tachycardia with narrow pulse pressure (< 20 mmHg)
Cold, clammy extremities
Delayed capillary refill (> 3 seconds)
Weak pulse
Restlessness or lethargy
Reduced urine output
Dengue Shock โ€“ Immediate Actions at Primary Care
Step Action
1
IV crystalloid bolus 10-20 mL/kg over 15-30 min
2 Reassess: If improving, reduce rate
3 If no improvement: Repeat bolus
4 If still no improvement: May need colloid (at higher centre)
5
TRANSFER URGENTLY
What NOT to Do in Dengue
โ›” Avoid
NSAIDs (Ibuprofen, Diclofenac) โ€“ increases bleeding
Aspirin โ€“ increases bleeding
IM injections โ€“ hematoma risk
Excessive IV fluids in recovery phase โ€“ pulmonary edema
Prophylactic platelet transfusion (not indicated unless severe bleeding or < 10,000)
Steroids (no proven benefit)
Primary Care Summary โ€“ Dengue
Scenario Action
No warning signs, tolerating orally Oral fluids, Paracetamol, monitor daily
Warning signs
IV fluids, TRANSFER
Shock
IV bolus 10-20 mL/kg, TRANSFER URGENTLY

4๏ธโƒฃ MALARIA โ€“ PRIMARY CARE MANAGEMENT

Classification
Category Features
Uncomplicated Malaria
Fever with positive test, no danger signs
Severe Malaria
Any danger sign present (see below)
Danger Signs (Severe Malaria)
Danger Sign Clinical Feature
Impaired consciousness
GCS < 11 or unable to sit/stand/localize pain
Prostration
Unable to walk or sit without support
Multiple convulsions
> 2 episodes in 24 hrs
Respiratory distress
Acidotic breathing, SpOโ‚‚ < 92%
Shock
SBP < 80 mmHg, cold extremities
Severe anemia
Hb < 5 g/dL or Hct < 15%
Jaundice
Visible icterus + parasitemia
Significant bleeding
Spontaneous bleeding
Hypoglycemia
Blood glucose < 40 mg/dL
Metabolic acidosis
pH < 7.25 or bicarbonate < 15
Renal impairment
Creatinine > 3 mg/dL or oliguria
Hyperparasitemia
> 10% parasitized RBCs (or > 250,000/μL)
Pulmonary edema/ARDS
Radiological evidence
Hemoglobinuria
Dark/black urine
Malaria Species in India
Species Prevalence Features
P. falciparum
~50%
Severe malaria, cerebral malaria, death
P. vivax
~50%
Relapsing; can cause severe disease
P. malariae
Rare
Chronic infection
P. ovale
Very rare
Similar to vivax
Mixed
Common
Both Pf and Pv
Diagnosis
Test When to Use
RDT (Rapid Diagnostic Test)
First-line in primary care
Peripheral smear
Gold standard; species identification; parasite count
QBC
If available; sensitive
Treatment โ€“ Uncomplicated P. falciparum or Mixed
Drug Dose Duration
Artesunate-Lumefantrine (AL)
Weight-based (see below)
3 days
OR Artesunate + Sulfadoxine-Pyrimethamine (AS+SP)
As per NVBDCP
3 days + single dose
+ Primaquine
0.25 mg/kg
Day 1 only (single dose for gametocidal)
Artesunate-Lumefantrine (Coartem) Dosing
Weight Tablets (20/120 mg) per dose Doses
5-14 kg
1 tablet
At 0, 8, 24, 36, 48, 60 hrs (6 doses)
15-24 kg
2 tablets
6 doses
25-34 kg
3 tablets
6 doses
≥ 35 kg
4 tablets
6 doses
Treatment โ€“ Uncomplicated P. vivax
Drug Dose Duration
Chloroquine
25 mg base/kg over 3 days (10+10+5 mg/kg)
3 days
+ Primaquine
0.25 mg/kg/day
14 days (for radical cure)
๐Ÿ“Œ Primaquine is contraindicated in G6PD deficiency and pregnancy โ€“ test if possible before 14-day course
Chloroquine Dosing (for P. vivax)
Day Dose (mg base/kg)
Day 1
10 mg/kg
Day 2
10 mg/kg
Day 3
5 mg/kg
Chloroquine-Resistant P. vivax
If Chloroquine-resistant area (NE India, some parts)
Use ACT (Artesunate-Lumefantrine) + Primaquine 14 days
Treatment โ€“ Severe Malaria
โš ๏ธ IV/IM Artesunate is the drug of choice
Drug Dose Route Timing
Artesunate
2.4 mg/kg
IV or IM
At 0, 12, 24 hrs, then every 24 hrs
If Artesunate unavailable:
Artemether
3.2 mg/kg loading, then 1.6 mg/kg
IM
Every 24 hrs
Quinine (last resort)
20 mg/kg loading, then 10 mg/kg
IV infusion
Every 8 hrs
Pre-Referral Dose (Before Transfer)
If Artesunate Available If Artesunate NOT Available
Artesunate 2.4 mg/kg IM/IV single dose Artemether 3.2 mg/kg IM single dose
Then transfer OR Quinine 20 mg/kg IV loading
๐Ÿ“Œ Give pre-referral dose and transfer immediately โ€“ do not delay
What NOT to Do in Malaria
โ›” Avoid
Chloroquine for P. falciparum (resistance widespread)
Oral treatment for severe malaria
Primaquine in pregnancy or G6PD deficiency
Delaying parenteral treatment for severe malaria
Primary Care Summary โ€“ Malaria
Scenario Action
Uncomplicated Pf or mixed ACT (Artesunate-Lumefantrine) × 3 days
Uncomplicated Pv Chloroquine × 3 days + Primaquine × 14 days
Severe / Any danger sign
Pre-referral Artesunate 2.4 mg/kg IM/IV → TRANSFER

5๏ธโƒฃ SCRUB TYPHUS โ€“ PRIMARY CARE MANAGEMENT

Key Features
Feature Details
Cause
Orientia tsutsugamushi (rickettsial)
Vector
Larval mites (chiggers)
Incubation
6-21 days
Classic triad
Fever + Eschar + Lymphadenopathy
Eschar
Painless, black, necrotic, often in hidden areas
Season
Post-monsoon (Sep-Nov) in India
Eschar โ€“ Highly Specific Finding
Eschar Characteristics
Painless black scab with erythematous halo
5-10 mm diameter
Often in hidden areas: axilla, groin, waist, behind ear
May be missed if not actively searched
Present in 40-80% cases
Common Eschar Locations (Search Carefully)
Location
Axilla
Groin / Inguinal area
Waistband area
Under breasts
Behind ears
Intergluteal fold
Scalp (in children)
Clinical Features
System Features
Constitutional
High fever, headache, myalgia
Skin
Eschar, maculopapular rash (trunk)
Lymph nodes
Regional lymphadenopathy (near eschar)
Respiratory
Cough, ARDS (common cause of mortality)
CNS
Meningoencephalitis, altered sensorium
Hepatic
Hepatomegaly, transaminitis
Renal
AKI
Cardiac
Myocarditis
Diagnosis
Test Timing Notes
Clinical (fever + eschar)
Any
Treat empirically if suspected
IgM ELISA
Day 7+
Most useful; may be negative early
Weil-Felix (OX-K)
Day 7+
Low sensitivity/specificity; avoid if possible
PCR
Any
Expensive; limited availability
๐Ÿ“Œ IgM may be negative in first week โ€“ if clinical suspicion is high, TREAT EMPIRICALLY
Treatment
Drug Dose Route Duration
Doxycycline (First-line)
100 mg BD
PO or IV
Until afebrile for 3 days (min 7 days)
Azithromycin (Alternative)
500 mg OD
PO or IV
5-7 days
Azithromycin (Pregnancy/Children < 8 yrs)
10 mg/kg Day 1, then 5 mg/kg
PO
5 days
Doxycycline in Children
Consideration Current Recommendation
Age < 8 years
May use Doxycycline for short courses in severe disease
Dental staining risk Minimal with short courses (< 21 days)
CDC/AAP Doxycycline is drug of choice for rickettsial diseases in all ages
Alternative Azithromycin 10 mg/kg/day
When to Suspect Scrub Typhus
Clinical Scenario
Fever > 5 days without focus
Post-monsoon season
Rural/agricultural area or travel to endemic region
Eschar present
ARDS/Respiratory failure with fever
Multi-organ dysfunction with fever
Not responding to usual antibiotics
Complications
Complication Management
ARDS
Oxygen, ventilation, continue Doxycycline
Shock
Fluids, vasopressors, Doxycycline
Meningoencephalitis
IV Doxycycline, supportive
Myocarditis
Supportive, Doxycycline
AKI
Fluids, may need dialysis
DIC
Supportive
Primary Care Summary โ€“ Scrub Typhus
Scenario Action
Suspected (fever + eschar/endemic area)
Start Doxycycline 100 mg BD immediately
Mild disease Doxycycline orally, monitor
Severe/MODS/ARDS
IV Doxycycline + TRANSFER
Pregnancy Azithromycin 500 mg OD × 5 days
Child < 8 yrs (severe) Doxycycline (CDC allows); OR Azithromycin
๐Ÿ“Œ Do NOT wait for serology โ€“ empiric Doxycycline is life-saving

6๏ธโƒฃ LEPTOSPIROSIS โ€“ PRIMARY CARE MANAGEMENT

Key Features
Feature Details
Cause
Leptospira interrogans (spirochete)
Source
Urine of infected animals (rats, dogs, cattle)
Transmission
Contact with contaminated water/soil through skin/mucosa
Incubation
5-14 days
Risk factors
Flooding, wading through water, agriculture, sewage work
Classic Clinical Features
Feature Description
Conjunctival suffusion
Redness without discharge โ€“ highly suggestive
Muscle tenderness
Especially calf muscles
Jaundice
Hepatorenal involvement
Oliguria
Renal failure
Hemorrhage
Pulmonary hemorrhage (severe form)
Clinical Spectrum
Form Features Mortality
Anicteric (Mild)
Fever, myalgia, headache, conjunctival suffusion
Low
Icteric (Weil's disease)
Jaundice + Renal failure + Hemorrhage
5-15%
Pulmonary hemorrhage (SPHS)
Massive hemoptysis, ARDS
50-70%
Danger Signs
Danger Sign
Jaundice
Oliguria / Anuria
Hemoptysis
Hypotension / Shock
Altered sensorium
Severe dyspnea
Bleeding manifestations
Diagnosis
Test Timing Notes
IgM ELISA
Day 5-7+
Most useful
MAT (Microscopic Agglutination Test)
Day 10+
Gold standard but delayed
Dark-field microscopy
First week
Low sensitivity
PCR
First week
If available
๐Ÿ“Œ Early in illness, tests may be negative โ€“ treat empirically if clinical suspicion high
Laboratory Findings
Finding Details
Leukocytosis Often with neutrophilia
Thrombocytopenia Mild-moderate
Elevated bilirubin Direct hyperbilirubinemia
Elevated creatinine Non-oliguric AKI common initially
Elevated transaminases Usually < 5× ULN (unlike viral hepatitis)
Elevated CPK Myositis
Abnormal urinalysis Proteinuria, pyuria, casts
Treatment
Severity Drug Dose Duration
Mild
Doxycycline
100 mg BD PO
7 days
OR Azithromycin
500 mg OD PO
3-5 days
OR Amoxicillin
500 mg TID PO
7 days
Severe
Ceftriaxone
1-2 g IV OD
7 days
OR Penicillin G
1.5 million units IV q6h
7 days
OR Doxycycline
100 mg IV BD
7 days
Jarisch-Herxheimer Reaction
Feature Details
Timing Within hours of first antibiotic dose
Features Fever spike, rigors, hypotension, tachycardia
Cause Release of bacterial toxins
Management Supportive; does NOT mean stop antibiotics
Primary Care Summary โ€“ Leptospirosis
Scenario Action
Suspected (flood exposure + fever + myalgia ± jaundice) Start Doxycycline 100 mg BD
Mild disease Oral Doxycycline, monitor
Severe / Jaundice / Renal impairment
IV Ceftriaxone 2g + TRANSFER
Hemoptysis / ARDS
IMMEDIATE TRANSFER

7๏ธโƒฃ ENTERIC FEVER (TYPHOID) โ€“ PRIMARY CARE MANAGEMENT

Key Features
Feature Details
Cause
Salmonella enterica serovar Typhi (or Paratyphi)
Transmission
Fecal-oral (contaminated water/food)
Incubation
7-21 days
Key feature
Stepladder fever, relative bradycardia, hepatosplenomegaly
Clinical Features
Week Features
Week 1
Gradually rising fever (stepladder), headache, malaise
Week 2
High sustained fever, abdominal pain, hepatosplenomegaly
Week 3-4
Complications: perforation, bleeding, encephalopathy
Characteristic Signs
Sign Description
Stepladder fever
Gradually rising temperature over days
Relative bradycardia
Pulse rate not matching fever (Faget sign)
Coated tongue
White coating with red edges
Hepatosplenomegaly
Soft, non-tender enlargement
Rose spots
2-4 mm salmon-colored macules on trunk (uncommon)
Abdominal tenderness
RIF (ileocecal region)
Diagnosis
Test Timing Notes
Blood culture
Week 1-2
Gold standard; sensitivity 60-80%
Widal test
Week 2+
Unreliable; avoid if possible
Typhidot IgM
Day 4+
More reliable than Widal
Stool culture
Week 2-3
Lower yield
Bone marrow culture
Any
Highest yield; rarely done
Problems with Widal Test
Issue
Single titre unreliable (endemic areas have baseline positivity)
False positives: Other Salmonella, cross-reactions, infections
False negatives: Early disease, antibiotic use
Requires paired sera (acute + convalescent) for confirmation
๐Ÿ“Œ Treat based on clinical suspicion + blood culture; do not rely solely on Widal
๐Ÿ‡ฎ๐Ÿ‡ณ Antibiotic Resistance in India
Resistance Pattern Current Status in India
Fluoroquinolone (Cipro, Levo)
80-90% resistance/reduced susceptibility
Chloramphenicol
Mostly sensitive now (resistance declined)
Ampicillin
Variable (40-60% resistant)
Cotrimoxazole
Variable
Ceftriaxone
< 5% resistance (first-line)
Azithromycin
< 5% resistance
Treatment โ€“ Uncomplicated Enteric Fever (India)
Drug Dose Route Duration
Ceftriaxone (First-line)
2 g OD
IV
10-14 days
75 mg/kg/day (child)
IV
10-14 days
Azithromycin (Alternative)
500 mg OD (or 1 g Day 1 then 500 mg)
PO
7 days
20 mg/kg/day (child)
PO
7 days
Cefixime (Oral, mild cases)
200 mg BD
PO
14 days
20 mg/kg/day (child)
PO
14 days
โš ๏ธ Do NOT use Fluoroquinolones (Ciprofloxacin, Levofloxacin) empirically in India โ€“ high resistance
Treatment โ€“ Severe / Complicated Enteric Fever
Drug Dose Route Duration
Ceftriaxone
2 g OD
IV
14 days
+ Consider Azithromycin
500 mg OD
IV/PO
7 days
For encephalopathy: Add Dexamethasone
3 mg/kg loading, then 1 mg/kg q6h
IV
48 hrs
Complications
Complication Timing Management
Intestinal perforation
Week 2-3
Surgical emergency
GI bleeding
Week 2-3
Transfusion, surgery if massive
Typhoid encephalopathy
Week 2-3
Dexamethasone + antibiotics
Myocarditis
Variable
Supportive
Relapse
Week 2 after stopping Rx
Repeat course of antibiotics
Chronic carrier
After recovery
Prolonged antibiotics (4-6 weeks)
Primary Care Summary โ€“ Enteric Fever
Scenario Action
Suspected enteric fever (clinical + endemic area) Ceftriaxone 2g IV OD OR Azithromycin 500 mg PO
Mild, tolerating orally Azithromycin 500 mg OD × 7 days or Cefixime 200 mg BD × 14 days
Severe / Complications
IV Ceftriaxone + TRANSFER

8๏ธโƒฃ EMPIRIC APPROACH โ€“ UNDIFFERENTIATED FEVER

When to Treat Empirically
Indication
Fever > 5 days with no clear focus
Endemic season (monsoon/post-monsoon)
Severe illness / Organ dysfunction
Clinical features suggestive of specific disease
Cannot wait for test results
Empiric Treatment at Primary Care
Clinical Scenario Empiric Treatment
Fever + Eschar (any area)
Doxycycline 100 mg BD (Scrub Typhus)
Fever + Flood/water exposure + Myalgia ± Jaundice
Doxycycline 100 mg BD OR Ceftriaxone 2g (Leptospirosis)
Fever + Splenomegaly + Endemic area
RDT for Malaria → ACT if positive
Fever + Thrombocytopenia + Monsoon
Suspect Dengue; monitor closely; fluids
Fever + Relative bradycardia + Hepatosplenomegaly
Ceftriaxone 2g (Enteric Fever)
Fever + ARDS/Multi-organ dysfunction
Doxycycline + Ceftriaxone (cover Scrub Typhus + Leptospirosis + Sepsis)
Combination Empiric Therapy (Severe Undifferentiated Fever)
Combination Covers
Doxycycline 100 mg IV BD + Ceftriaxone 2g IV OD
Scrub Typhus, Leptospirosis, Enteric Fever, Bacterial sepsis
Add Artesunate 2.4 mg/kg IV If Malaria cannot be ruled out
๐Ÿ“Œ This combination covers most life-threatening tropical infections

9๏ธโƒฃ TRANSFER PROTOCOL

Transfer Indications
Condition Transfer Indication
Dengue
Any warning sign, severe dengue, shock
Malaria
Any danger sign, severe malaria
Scrub Typhus
ARDS, shock, encephalitis, MODS
Leptospirosis
Jaundice, renal failure, pulmonary hemorrhage
Enteric Fever
Perforation, bleeding, encephalopathy
Any
Not responding to treatment, deteriorating
Pre-Transfer Checklist
Item Done?
IV access secured
โ˜
IV fluids running (appropriate rate)
โ˜
Empiric antibiotics/antimalarials given
โ˜
Blood glucose checked
โ˜
Vital signs documented
โ˜
All investigations documented
โ˜
Receiving hospital pre-alerted
โ˜

๐Ÿ”ต PART 2 โ€” SECONDARY/TERTIARY CARE


๐Ÿ”Ÿ EMERGENCY DEPARTMENT PROTOCOL

Immediate Assessment
Action Target Time
Primary survey (ABCDE)
Immediate
Blood glucose
≤ 5 min
IV access (if not present)
≤ 10 min
Draw blood samples
≤ 15 min
Rapid tests (Dengue, Malaria)
≤ 30 min
Empiric treatment (if indicated)
≤ 1 hour
Investigations
Investigation Purpose
CBC with differential
Thrombocytopenia, leukopenia/leukocytosis
Peripheral smear
Malaria parasites, platelet count
Malaria RDT
Rapid diagnosis
Dengue NS1/IgM combo
Dengue confirmation
Liver function (LFT)
Hepatic involvement
Renal function (RFT)
AKI
Blood glucose
Hypoglycemia (malaria)
Electrolytes
Hyponatremia, hypokalemia
Coagulation (PT, aPTT)
Coagulopathy
ABG
Acidosis, oxygenation
Blood cultures
Bacterial infection, enteric fever
Urine analysis
Proteinuria (leptospirosis)
Chest X-ray
ARDS, pulmonary edema, hemorrhage
Lactate
Tissue perfusion
Procalcitonin
Bacterial vs viral differentiation
Scrub Typhus IgM
If suspected
Leptospira IgM
If suspected

1๏ธโƒฃ1๏ธโƒฃ DENGUE โ€“ SECONDARY CARE MANAGEMENT

Severe Dengue โ€“ Definition
Category Features
Severe plasma leakage
Shock (DSS), fluid accumulation with respiratory distress
Severe bleeding
GI bleeding, menorrhagia, etc.
Severe organ impairment
Liver (AST/ALT > 1000), CNS (encephalopathy), Heart (myocarditis)
Dengue Shock Syndrome (DSS) Management
Step Action
1
Crystalloid bolus 10-20 mL/kg over 15-30 min
2 Reassess (BP, pulse, Hct, urine output)
3 If improving: Reduce rate stepwise
4 If not improving: Repeat crystalloid bolus
5
If still not improving: Colloid 10-20 mL/kg (Dextran 40 or Starch)
6 If refractory: Blood transfusion if Hct falling
Fluid Algorithm โ€“ Compensated Shock
Time Action
0-1 hr
NS/RL 10-20 mL/kg over 1 hr
1-2 hr
If improving: 10 mL/kg over 1 hr
2-3 hr
If stable: 7 mL/kg/hr
3-4 hr
Reduce to 5 mL/kg/hr
Next
Stepwise reduction
Fluid Algorithm โ€“ Hypotensive Shock
Step Action
1 Crystalloid bolus 20 mL/kg over 15-30 min
2 If no improvement: Repeat crystalloid 10-20 mL/kg
3 If still no improvement: Colloid 10-20 mL/kg
4 If Hct dropping: Blood transfusion
5 If Hct rising despite fluids: Consider more colloid
Hematocrit Interpretation
Hct Change Interpretation Action
Rising Hct Ongoing plasma leak More IV fluids
Falling Hct rapidly Occult bleeding Blood transfusion
Stable Hct Adequate resuscitation Maintain fluids
Blood Product Transfusion
Packed RBCs Significant bleeding + Hct drop Hct > 30%
Platelets
Active bleeding + platelets < 20,000 โ€”
Anticipated procedure + platelets < 50,000 โ€”
โ›” NOT indicated prophylactically โ€”
FFP
Coagulopathy with bleeding Correct PT/aPTT
๐Ÿ“Œ Prophylactic platelet transfusion is NOT recommended in dengue
Monitoring in Severe Dengue
Parameter Frequency
Vitals (BP, HR, RR)
Every 15-30 min in shock; hourly if stable
Hct
Every 4-6 hrs (more frequent in shock)
Urine output
Hourly (catheterize if needed)
Blood glucose
Every 4-6 hrs
Platelet count
Daily
Clinical assessment
Continuous
Recovery Phase Management
Issue Management
Fluid overload
Stop IV fluids; oral fluids only; diuretics if needed
Pulmonary edema
Diuretics, oxygen, reduce IV fluids
Bradycardia
Normal in recovery; monitor
Rash (confluent with islands of sparing)
Common; self-limiting

1๏ธโƒฃ2๏ธโƒฃ SEVERE MALARIA โ€“ SECONDARY CARE MANAGEMENT

IV Artesunate Protocol
Timing Dose
0 hours
2.4 mg/kg IV
12 hours
2.4 mg/kg IV
24 hours
2.4 mg/kg IV
Then
2.4 mg/kg IV every 24 hrs
Duration
Until patient can take oral; minimum 24 hrs (3 doses)
Follow with
Oral ACT to complete 3 days
Artesunate Preparation
Preparation Details
Vial contents 60 mg powder + solvent
Reconstitute With 1 mL 5% sodium bicarbonate
Dilute With 5 mL NS to get 10 mg/mL
Administration IV bolus over 1-2 min OR IM
Artesunate Dose Calculation
Weight (kg) Dose (2.4 mg/kg) Volume (10 mg/mL)
40
96 mg
9.6 mL
50
120 mg
12 mL
60
144 mg
14.4 mL
70
168 mg
16.8 mL
80
192 mg
19.2 mL
Specific Complications โ€“ Management
Complication Management
Cerebral malaria
Artesunate; avoid lumbar puncture if raised ICP; seizure control; nursing care
Severe anemia (Hb < 5)
Blood transfusion; target Hb > 7 g/dL
Hypoglycemia
50% dextrose 50 mL IV; D10% infusion; monitor closely
AKI
Fluids; may need dialysis
ARDS
Low tidal volume ventilation; minimize fluids
Acidosis
Treat underlying cause; fluids; may need bicarbonate if pH < 7.1
Shock
Fluids; vasopressors; exclude gram-negative sepsis
DIC
Supportive; blood products if bleeding
Blackwater fever
Fluids; transfusion; stop quinine if being used
Post-Artesunate Delayed Hemolysis (PADH)
Feature Details
Timing 7-21 days after artesunate treatment
Mechanism Delayed clearance of pitted RBCs
Features Recurrent anemia, jaundice, hemolysis
Risk More common in non-immune travelers; high parasitemia
Management Monitor Hb weekly × 4 weeks; transfuse if needed
Primaquine in Severe Malaria
For P. falciparum For P. vivax
Single dose 0.25 mg/kg after recovery 14-day course 0.25 mg/kg/day after recovery
Gametocidal Radical cure (anti-hypnozoite)
Check G6PD if possible Check G6PD before 14-day course

1๏ธโƒฃ3๏ธโƒฃ SCRUB TYPHUS โ€“ SECONDARY CARE MANAGEMENT

IV Doxycycline Protocol
Drug Dose Frequency Duration
Doxycycline
100 mg (or 2.2 mg/kg)
BD
at least until 3 days of fever resolution (min 7-14 days)
Doxycycline Preparation for IV Use
Preparation Details
Doxycycline vial 100 mg powder
Reconstitute With 10 mL sterile water
Dilute In 100-250 mL NS or D5W
Infuse Over 1-4 hours
โš ๏ธ Avoid Rapid infusion (thrombophlebitis)
Adjunctive Therapies
Therapy Indication Notes
Steroids
ARDS, shock, myocarditis Controversial; some use methylprednisolone 1-2 mg/kg
Vasopressors
Refractory shock Norepinephrine first-line
Mechanical ventilation
ARDS Lung-protective strategy
Dialysis
AKI with indication Standard RRT indications
Monitoring
Parameter Frequency
Temperature
Every 4-6 hrs
Vitals
Continuous/hourly if unstable
SpOโ‚‚
Continuous
Urine output
Hourly
LFT, RFT
Daily
Chest X-ray
Daily if ARDS
Expected Response
Response Timing
Defervescence Within 24-48 hrs of Doxycycline
Clinical improvement 48-72 hrs
If no response by 72 hrs Reconsider diagnosis; ensure compliance

1๏ธโƒฃ4๏ธโƒฃ LEPTOSPIROSIS โ€“ SECONDARY CARE MANAGEMENT

Antibiotic Protocol
Severity Drug Dose Duration
Severe
Ceftriaxone
1-2 g IV OD
7 days
OR Penicillin G
1.5 million units IV q6h
7 days
OR Doxycycline
100 mg IV BD
7 days
Severe Pulmonary Hemorrhage Syndrome (SPHS)
Management Details
Antibiotics
IV Ceftriaxone or Penicillin immediately
Oxygen
High-flow; may need intubation
Mechanical ventilation
Lung-protective; PEEP
Blood transfusion
If significant blood loss
Steroids
Controversial; Methylprednisolone 1 g IV × 3 days used in some centres
Plasma exchange
Case reports of benefit
ECMO
Last resort
๐Ÿ“Œ SPHS has very high mortality (50-70%); early recognition and aggressive ICU care is essential
Weil's Disease (Icteric Leptospirosis)
Feature Management
Jaundice Antibiotics; supportive
Hepatorenal syndrome Fluids; dialysis if needed
Coagulopathy Vitamin K, FFP if bleeding
Thrombocytopenia Usually mild; transfuse if bleeding
Dialysis Indications
Indication
Oliguria/anuria not responding to fluids
Severe hyperkalemia
Refractory acidosis
Uremic complications
Fluid overload

1๏ธโƒฃ5๏ธโƒฃ ENTERIC FEVER โ€“ SECONDARY CARE MANAGEMENT

IV Antibiotic Protocol
Drug Dose Duration
Ceftriaxone
2 g IV OD (75 mg/kg/day in children)
10-14 days
+ Azithromycin (severe cases)
500 mg IV/PO OD
7 days
Complicated Enteric Fever
Typhoid Encephalopathy
Treatment Dose
Dexamethasone
3 mg/kg IV loading over 30 min
Then
1 mg/kg IV every 6 hrs × 8 doses (48 hrs)
Continue
IV Ceftriaxone
๐Ÿ“Œ Dexamethasone reduces mortality in severe typhoid encephalopathy (Hoffman trial)
Intestinal Perforation
Management
Surgical emergency
NPO
IV fluids
IV antibiotics (Ceftriaxone + Metronidazole)
Urgent surgery โ€“ primary repair or resection
GI Bleeding
Management
NPO
IV fluids
Blood transfusion if needed
Correct coagulopathy
Surgery if massive/uncontrolled
Relapse and Chronic Carrier
Scenario Treatment
Relapse (fever returns after stopping Rx)
Repeat full course of antibiotics
Chronic carrier (stool positive > 1 year)
Ciprofloxacin 750 mg BD × 4 weeks OR Amoxicillin 2g TID + Probenecid × 6 weeks OR Cholecystectomy (if gallstones)

1๏ธโƒฃ6๏ธโƒฃ COINFECTIONS & OVERLAPPING SYNDROMES

Common Coinfections in India
Coinfection Scenario
Dengue + Malaria Common in endemic areas during monsoon
Dengue + Scrub Typhus Post-monsoon period
Scrub Typhus + Leptospirosis Both post-monsoon; similar exposures
Malaria + Enteric Fever Endemic areas
Approach to Possible Coinfection
Principle Action
Test for multiple diseases Especially if atypical features
Treat for most life-threatening first Malaria, Scrub Typhus
Combination empiric therapy If undifferentiated and severe
Monitor response Modify treatment based on results
Empiric Combination for Severe Undifferentiated Fever
Combination Covers
Ceftriaxone 2g IV OD
Enteric fever, Leptospirosis, Bacterial sepsis
+ Doxycycline 100 mg IV BD
Scrub Typhus, Leptospirosis
+ Artesunate 2.4 mg/kg IV
Malaria (if cannot be ruled out)

1๏ธโƒฃ7๏ธโƒฃ SUPPORTIVE CARE (ALL)

ICU Monitoring
Parameter Frequency
Vitals
Continuous/hourly
SpOโ‚‚
Continuous
Urine output
Hourly
Blood glucose
4-6 hourly
Hematocrit (Dengue)
4-6 hourly
Parasitemia (Malaria)
Every 12-24 hrs until negative
LFT, RFT, Coagulation
Daily
Supportive Measures
Aspect Recommendation
Fluids
Careful titration; avoid overload
Glucose
Maintain euglycemia; D10% if hypoglycemic
Electrolytes
Correct abnormalities
Nutrition
Enteral preferred; start early if stable
DVT prophylaxis
Mechanical (IPC); avoid pharmacological if bleeding risk
Stress ulcer prophylaxis
PPI if high-risk
Fever
Paracetamol; avoid NSAIDs in Dengue

1๏ธโƒฃ8๏ธโƒฃ DISCHARGE PLANNING

Discharge Criteria
Disease Discharge Criteria
Dengue
No fever × 48 hrs without antipyretics; improving appetite; stable Hct; platelets rising; no warning signs
Malaria
Completed treatment; afebrile; tolerating orally; parasitemia clearing
Scrub Typhus
Afebrile × 3 days; stable; completing oral Doxycycline
Leptospirosis
Afebrile; renal function stable/improving; completing antibiotics
Enteric Fever
Afebrile × 5-7 days; tolerating orally; no complications
Follow-up
Disease Follow-up
Dengue
Review in 1 week; watch for delayed recovery
Malaria (Pf)
Day 28 smear; watch for PADH (Hb check weekly × 4)
Malaria (Pv)
Complete Primaquine 14 days; watch for relapse
Scrub Typhus
Complete antibiotics; watch for relapse
Leptospirosis
Renal function check; complete antibiotics
Enteric Fever
Stool culture to confirm clearance (especially food handlers)

๐Ÿ“Œ QUICK REFERENCE CARDS

๐Ÿ”ด PRIMARY CARE โ€“ TROPICAL FEVER CARD

text
โ•”โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•—
โ•‘ TROPICAL FEVER โ€“ PRIMARY CARE โ•‘
โ• โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•ฃ
โ•‘ โ•‘
โ•‘ 1. CHECK BLOOD GLUCOSE + VITALS + RAPID TESTS โ•‘
โ•‘ โ•‘
โ•‘ โ”Œโ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ” โ•‘
โ•‘ โ”‚ ESCHAR (painless black scab) → SCRUB TYPHUS โ”‚ โ•‘
โ•‘ โ”‚ → Doxycycline 100 mg BD immediately โ”‚ โ•‘
โ•‘ โ””โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”˜ โ•‘
โ•‘ โ•‘
โ•‘ โ”Œโ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ” โ•‘
โ•‘ โ”‚ MALARIA RDT POSITIVE → MALARIA โ”‚ โ•‘
โ•‘ โ”‚ → Uncomplicated: ACT (Artesunate-Lumefantrine) โ”‚ โ•‘
โ•‘ โ”‚ → Severe/Danger signs: Artesunate 2.4 mg/kg IV → TRANSFER โ”‚ โ•‘
โ•‘ โ””โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”˜ โ•‘
โ•‘ โ•‘
โ•‘ โ”Œโ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ” โ•‘
โ•‘ โ”‚ DENGUE NS1/IgM POSITIVE + THROMBOCYTOPENIA → DENGUE โ”‚ โ•‘
โ•‘ โ”‚ → No warning signs: Oral fluids, Paracetamol, Monitor โ”‚ โ•‘
โ•‘ โ”‚ → Warning signs/Shock: IV fluids → TRANSFER โ”‚ โ•‘
โ•‘ โ””โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”˜ โ•‘
โ•‘ โ•‘
โ•‘ โ”Œโ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ” โ•‘
โ•‘ โ”‚ FLOOD EXPOSURE + JAUNDICE + MYALGIA → LEPTOSPIROSIS โ”‚ โ•‘
โ•‘ โ”‚ → Doxycycline 100 mg BD OR Ceftriaxone 2g IV โ”‚ โ•‘
โ•‘ โ””โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”˜ โ•‘
โ•‘ โ•‘
โ•‘ โ”Œโ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ” โ•‘
โ•‘ โ”‚ RELATIVE BRADYCARDIA + HEPATOSPLENOMEGALY → ENTERIC FEVER โ”‚ โ•‘
โ•‘ โ”‚ → Ceftriaxone 2g IV OD (NOT Ciprofloxacin โ€“ 80%+ resistance) โ”‚ โ•‘
โ•‘ โ””โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”€โ”˜ โ•‘
โ•‘ โ•‘
โ•šโ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•โ•

๐Ÿ’Š ANTIBIOTIC QUICK REFERENCE (INDIA-SPECIFIC)

Disease First-Line Alternative Duration
Scrub Typhus
Doxycycline 100 mg BD Azithromycin 500 mg OD
7-14 days
Leptospirosis
Ceftriaxone 2g IV OD Doxycycline 100 mg BD
7 days
Enteric Fever
Ceftriaxone 2g IV OD Azithromycin 500 mg OD
10-14 days
Severe Malaria
Artesunate 2.4 mg/kg IV Artemether IM
Until oral; then ACT
Uncomplicated Malaria (Pf)
ACT (Artesunate-Lumefantrine) โ€”
3 days
Uncomplicated Malaria (Pv)
Chloroquine + Primaquine ACT + Primaquine
3d + 14d
Dengue
โ›” No antibiotics โ€”
โ€”

๐Ÿšจ DANGER SIGNS SUMMARY

Disease Danger Signs → Transfer Immediately
Dengue
Abdominal pain, persistent vomiting, fluid accumulation, mucosal bleeding, lethargy, Hct rise + plt drop, shock
Malaria
Impaired consciousness, prostration, convulsions, respiratory distress, shock, Hb < 5, hypoglycemia, oliguria, jaundice
Scrub Typhus
ARDS, shock, encephalopathy, multi-organ dysfunction
Leptospirosis
Jaundice, oliguria, hemoptysis, shock, altered sensorium
Enteric Fever
Encephalopathy, perforation (abdominal rigidity), massive GI bleed

๐ŸŒก๏ธ DIFFERENTIATION TABLE

Feature Dengue Malaria Scrub Typhus Leptospirosis Enteric Fever
Eschar
โŒ
โŒ
โœ…
โŒ
โŒ
Conjunctival suffusion
โŒ
โŒ
โŒ
โœ…
โŒ
Relative bradycardia
โŒ
โŒ
โš ๏ธ
โŒ
โœ…
Severe thrombocytopenia
โœ…
โš ๏ธ
โš ๏ธ
โš ๏ธ
โš ๏ธ
Jaundice
Rare
โš ๏ธ
โš ๏ธ
โœ…
Rare
Calf tenderness
โŒ
โŒ
โŒ
โœ…
โŒ
Splenomegaly
โš ๏ธ
โœ…
โš ๏ธ
โš ๏ธ
โœ…
ARDS
โš ๏ธ
โš ๏ธ
โœ…
โœ…
Rare

โš ๏ธ CRITICAL WARNINGS

โ›” NEVER โœ… ALWAYS
Use NSAIDs/Aspirin in Dengue Use Paracetamol for fever
Use Ciprofloxacin for Enteric Fever in India (80%+ resistance) Use Ceftriaxone or Azithromycin
Give oral treatment for severe Malaria Give IV/IM Artesunate for severe Malaria
Ignore eschar in fever Search for eschar (hidden areas); treat for Scrub Typhus
Wait for serology to treat Scrub Typhus Treat empirically with Doxycycline if suspected
Give prophylactic platelets in Dengue Transfuse only for active bleeding + very low count
Forget Primaquine in P. vivax Give 14-day Primaquine for radical cure (check G6PD)
Overload fluids in recovery phase of Dengue Reduce fluids as patient improves

๐Ÿ‡ฎ๐Ÿ‡ณ INDIA-SPECIFIC REMINDERS

Situation Remember
Monsoon fever + thrombocytopenia Think Dengue first
Post-monsoon fever + eschar Scrub Typhus until proven otherwise
Flood exposure + fever + jaundice Leptospirosis
Endemic area + fever + splenomegaly Malaria
Fever > 7 days + relative bradycardia Enteric Fever
ARDS with fever in post-monsoon Scrub Typhus or Leptospirosis
Undifferentiated severe fever Doxycycline + Ceftriaxone ± Artesunate
Enteric fever antibiotics NO Fluoroquinolones empirically

๐Ÿ“š ABBREVIATIONS

Abbreviation Full Form
ACT
Artemisinin-based Combination Therapy
AL
Artesunate-Lumefantrine
AS+SP
Artesunate + Sulfadoxine-Pyrimethamine
RDT
Rapid Diagnostic Test
NS1
Non-Structural Protein 1
DSS
Dengue Shock Syndrome
Hct
Hematocrit
PADH
Post-Artesunate Delayed Hemolysis
G6PD
Glucose-6-Phosphate Dehydrogenase
SPHS
Severe Pulmonary Hemorrhage Syndrome
MAT
Microscopic Agglutination Test
ARDS
Acute Respiratory Distress Syndrome
MODS
Multi-Organ Dysfunction Syndrome
AKI
Acute Kidney Injury
DIC
Disseminated Intravascular Coagulation
RFT
Renal Function Tests
LFT
Liver Function Tests
Pf
Plasmodium falciparum
Pv
Plasmodium vivax
JE
Japanese Encephalitis
NVBDCP
National Vector Borne Disease Control Programme
IPC
Intermittent Pneumatic Compression
FFP
Fresh Frozen Plasma
NS
Normal Saline
RL
Ringer's Lactate
OD
Once Daily
BD
Twice Daily
TID
Three Times Daily
q6h
Every 6 hours

๐Ÿ“– REFERENCES

Guideline/Source Year
WHO Guidelines on Dengue
2009, 2012
National Guidelines on Dengue (NVBDCP, India) 2022
WHO Guidelines on Severe Malaria
2015, 2021
National Framework for Malaria Elimination (India) 2016
ICMR Guidelines on Scrub Typhus 2021
IAP-RCPCH Guidelines on Scrub Typhus 2021
WHO Guidelines on Leptospirosis 2003
ICMR Antimicrobial Resistance Surveillance 2022
API Textbook of Medicine
Latest Edition
Indian Journal of Medical Research โ€“ Tropical Fever Reviews
Various

Document Version: 1.0
India-Specific Notes:
  • High fluoroquinolone resistance in Enteric Fever โ€“ avoid Ciprofloxacin empirically
  • Scrub Typhus is underdiagnosed โ€“ always search for eschar
  • Coinfections are common in monsoon season
  • Doxycycline + Ceftriaxone covers most severe tropical infections
  • Artesunate is first-line for severe malaria (not Quinine)
Disclaimer: This protocol provides general guidance. Clinical judgment must be exercised. Local epidemiology and resistance patterns should guide treatment. Regional NVBDCP and state health guidelines may have specific recommendations.
๐Ÿ›ก๏ธ

Medical Advisory

Clinical guidelines are subject to change. Physicians should exercise their regular clinical judgment. This protocol does not replace individual institutional policies. Verified for Q1 2026.

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