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PYREXIA OF
UNKNOWN ORIGIN
PRESENTED BY:
TANVI SINGLA
Regulates normal body temperature
Normal Rectal temp. being
97.7-99.5°F
Oral temp. being 0.7°F
lower than rectal
while axillary being 1.2°F
lower than rectal.
Daily normal variation
being 0.5-1°F
With evening temperatures
being higher than the
morning
If body temp. exceeds
normal variation in an
individual, that’s called
FEVER
Liebermiester’s Rule: With each degree centigrade
rise in body temp. , heart rate increase by 8 per min
Except in those diseases where relative bradycardia
sets in.
DEFINITION
PETERSDORF
AND BEESON
1961
TEMP> 101°F
ON SEVERAL
OCCASIONS
DURATION OF
FEVER > 3
WEEKS
FAILURE TO REACH
DIAGNOSIS
DESPITE 1 WEEK OF
INPATIENT INV.
DURACK & STREET’S CLASSIFICATION
CLASSIC
PUO
• 3 OUTPATIENT VISITS OR 3 DAYS IN HOSPITAL W/O ELUCIDATION OF CAUSE
• OR 1 WEEK OF “INTELLIGENT AND INVASIVE” AMBULATORY INV.
NOSOCOMIAL
PUO
•IN HOSPITALISED PATIENTS TEMP> 101°F DEVELOPS ON SEVERAL OCCASIONS WHO IS
RECEIVING ACUTE CARE AND WHOM WAS NOT MANIFEST OR INCUBATING AT TIME OF
ADMISSION
•3 DAYS OF INV. INCLUDING ATLEAST 2 DAYS INCUBATION OF CULTURES
NEUTROPENIC
PUO
•TEMP> 101°F ON SEVERAL OCCASIONS IN PATIENTS WHOSE NEUTROPHIL
COUNT IS <500uL(n 2-7x10^3) OR EXPECTED TO FALL WITHIN 1-2 DAYS
•NO SPECIFIC CAUSE IDENTIFIED 3 DAYS OF INV. INCLUDING ATLEAST 2 DAYS INCUBATION OF
CULTURES
HIV-
ASSOCIATED
PUO
• >101°F ON SEVERAL OCCASIONS OVER A PERIOD OF >4 WEEKS FOR
OUTPT. OR >3 DAYS FOR INPT. WITH HIV
•NO SOURCE REVELAED OVER 3 DAYS INV. INCLUDING 2 DAYS
INCUBATION OF CULTURES
COMMON CAUSES OF PUO
TB being the no. 1
DRUG FEVER
INFECTIONS
Bacterial Infection: Common etiologies
•Chronic sinusitis
•Mastoiditis
•Salmonellosis
•Abscesses(subdiaphragmatic,liver,renal,retroperitoneal,
paraspinal)
•Chronic prostatitis
•Pyelonephritis
•Bacterial endocarditis(esp if caused by HACEK group)
•Osteomyelitis(esp in cases of implantation of
prostheses)
Uncommon
•Leptospirosis
•Brucellosis
•Chlamydia
•Rickettsial infections(Q fever, Scrub Typhus,
Rocky Mountain Spotted fever)
•TB meningitis
•Spinal TB
•Bone and joint TB
•Grannulomatous hepatitis
•Abdominal TB
•Genitourinary TB
•Tubercular lymphadenopathy
VIRAL:
• CMV
•EBV
•HIV
FUNGAL:
•Blastomycosis
•Histoplasmosis
•Cryptococcus
PARASITIC
•Malaria
•Toxoplasmosis
•Leishmaniasis
NEOPLASMS
All kinds of
AUTO-IMMUNE DISORDERS
•SLE
•Vasculitis
•Adult still’s disease
•Temporal arteritis
MISCELLANEOUS
Hyperthyroidism
Phaechromocytoma
Metabolic disorders
DRUG FEVER:
•Antimicrobials(Beta lactum
antibiotics)
•Cardiovascular (Quinidine)
•Antineoplastic
•Antiepileptic (phenytoin)
A 45 year old man was admitted to the ICU
with acute MI, thrombolysed and
reperfused, but then went into persistent
hypotension following a cardiac arrest. He
developed fever on Day 5. Routine blood
investigation showed a polymorpho-
nuclear leucocytosis. Blood culture was
diagnostic.
What could it be???
NOSOCOMIAL PUO
ETIOLOGY
Infections
Non infectious cause
Undiagnosed
Others
•Accounts for 50%
• suspects will be I/V lines, prothesis, septic
phlebitis
•Focused approach on sites where occult
infection may be present eg sinuses of intubated
patients.
Accounts for 25%
•Acalculous cholecystitis
•DVT
•Pulmonary Embolism
Includes drug fever,
withdrawal or
transfusion rxns or post
myocardial infarction
syndrome.
20% remains undiagnosed
A 14 year old boy was admitted with high grade
fever and pallor. On examination no
hepatosplenomegaly, lymphadenopathy or bone
tenderness were present. The blood counts were
as follows: Hb 8gm%, TLC 3800, P8 L86 E4 M2,
ESR 20 mm in 1st hr. Platelet count 2.5 lakhs.
What could it be???
NEUTROPENIC INFECTIONS
Patients on chemotherapy or immune deficiencies are more
susceptible to:
•Oppurtunistic bacterial infections
•Fungal infections like candidiasis
•Bacteremic infections
•Infections involving catheters
•Perianal infections
Most common etiological agents are:
•Aspergillus
•Candida
•CMV
•Herpes simplex
HIV – associated PUO
HIV Infection as such may be the cause
Other secondary causes are:
Pulmonary Tuberculosis
Pneumocystis Infection
Toxoplasmosis
Salmonellosis
Cryptococciosis
Cytomegalovirus infection
M. Avium or M. Intracellulare
Non-Hodgkin’s Lymphoma
Drug induced fever
PYREXIA
OF
UNKNOWN
ORIGIN
- A CLINICAL
APPROACH
HISTORY TAKING
History of present illness
1)Onset :
• Acute: Malaria, pyogenic infection
• Gradual: TB, typhoid fever
2) Character:
high grade- UTI, TB, malaria, drug
3) Pattern: Whether returns to normal or not
• Sustained/ persistent: typhoid, drugs
•Intermittent fever:
Daily spikes: Abscesses, TB, Schistosomiasis
Twice – daily spikes: Leishmaniasis
•Relapsing/recurrent fever: Non falciparum malaria,
Brucellosis, Hodgkin’s
4) Antecedents
-Prior to onset of fever:
•Dental extraction: infective endocarditis
•Urinary catheterization: UTI, bacteremia
5) Associated symptoms:
• Rigors and chills
 Bacterial, rickettsial and protozoal disease
Influenza, lyphoma, leukaemia, drug-induced
•Night sweats: TB, Hodgkin’s lymphoma
•Loss of weight: malignancy, TB
•Cough and dyspnoea: miliary TB, multiple pulm.
Emboli, CMV
•Headache: Giant cell arteritis
•Joint pain: RA,SLE, vasculitis
• Abd. Pain
– Cholangitis, biliary obstruction, perinephric abscess,
Crohn’s disease, dissecting aneuryms,
gynaecological infection
• Bone pain
– Osteomyelitis, lymphoma
• Sorethroat
– IM, retropharyngeal abscess, post-Streptococcal
infection
• Dysuria, rectal pain
– Prostatic abscess, UTI
• Altered bowel habit
– IBD, typhoid fever, schistosomiasis, amoebiasis
• Skin rash
– Gonococcal infection, PAN,NHL, dengue fever
• Past Medical History
– Malignancy = leukemia, lymphoma, hepatocellular ca
– HIV infection
– DM
– IBD
– collagen vascular disease-SLE, RA, giant cell arteritis
– TB
– Heart disease: valvular heart disease
• Past Surgical History
– Post splenectomy/ post- transplantation
– Prosthetic heart valve
– Catheter, AV fistula
– Recent surgery/ operation
• Drug History
– Drug fever occur within 3 months after
start of drugs
• may cause low grade fever, usually
associated with rash
• Due to the allergic reaction, direct effect of
drug which impair temperature regulation
(e.g. phenothiazine)
• E.g. Antiarrhythmic drug: procainamide,
quinidine; Antimicrobial agent: penicillin,
cephalosporin, hydralazine
– After fever: may modify clinical pictures,
mask certain infection e.g. SBE, antibiotic
allergy
Family History
–Anyone in family has similar problem:
TB, familial Mediterranian fever
• Social History
– Travel
• amoebiasis, typhoid fever, malaria,
Schistosomiasis
– Residental area
• malaria, leptospirosis, brucellosis
– Occupation
• farmers, veterinarian, slaughter-house workers =
Brucellosis
• workers in the plastic industries = polymer-fume
fever
–Contact with domestic / wild animal /
birds :
• Brucellosis, psittacosis (pigeons),
Leptospirosis, Q fever, Toxoplasmosis
–Diet history
• unpasteurized milk/cheese =
Brucellosis
• poorly cooked pork = Trichinosis
–Sexual orientation = HIV, STD, PID
–Close contact with TB patients
EXAMINATION
• General
Calm, conscious, oriented to time, place
and person
Ill/not ill
Built/Weight loss (chronic illness)
Vitals
CLIPJES(Skin rash)
HEAD AND NECK
• Feel temporal arteries (tender & thicken)
• Eyes – iritis/conjuctivitis (ct disease –
reiter syndrome)
• Jaundice (ascending cholangitis)
• Fundi – choroidal tubercle (miliary tb),
roth’s spot (ie) and retinal haemorrhage
(leukaemia)
• Lymphadenopathy
FACE AND MOUTH
• Butterfly rash
• Mucous membranes
• Seborrhoic dermatitis (HIV)
• Mouth ulcers (SLE)
• Buccal candidiasis
• Teeth & tonsils infection (abscess)
• Parotid enlargement
• Ears – otitis media
HANDS
• Stigmata of Infective Endocarditis
• Vasculitis changes
• Clubbing
• Presence of arthropathy
• Raynaud’s phenomenon
ARMS
• Drug injection sites
• Axillary nodes (lymphoma, sarcoidosis,
focal infection)
• Skin
CHEST
• Bony tenderness
• CVS – murmurs (ie atrial myxoma), rubs
(pericarditis)
• Resp – signs of pneumonia, TB, empyema
and lung ca
ABDOMEN
• Rose coloured spot
(typhoid fever)
• Hepatomegaly
(hepatic ca,
alcoholic hepatitis)
• Splenomegaly
(haemopoietic
malignancy,
malaria)
• Renal enlargement
(renal cell ca)
• Testicular
enlargement
(seminoma)
• Penis & scrotum –
discharge/rash
• Inguinal ligament
• Per rectal exam – mass/tenderness in
rectum/pelvis (abscess, ca, prostatitis)
• Vaginal Examination – collection of pelvic
pus/ Pelvic Inflammatory Disease
CENTRAL NERVOUS SYSTEM
• Signs of meningism (chronic tb meningitis)
• Focal neurological signs (brain abscess,
mononeuritis multiplex in polyarteritis
nodosa)
STAGE 1: LAB INVESTIAGTIONS
Stage 1: (screening tests)
1. Full blood count
(evalute anaemia, +nce of
blasts, thrombocytopenia)
2. ESR & CRP
3. LFTs
4. Blood culture
5. Serum virology
(EBV,CMV)
6. M/b panel
(LFT,LDH,creatinine)
7. Urinalysis and
culture
8. Sputum culture and
sensitivity
9. Stool and occult
blood
10. CXR
11. Mantoux test
STAGE 2: LAB INVESTIGATIONS
1. Repeat history and
examination
2. Protein
electrophoresis
3. CT (chest, abdomen,
pelvis)
4. Autoantibody
screen (ANA, RF,
ANCA, anti-dsDNA)
5. Echocardiography
6. Bone scan(osteomye.)
7. Lumbar puncture
8. Consider PSA, CEA
9. Temporal artery
biopsy
10.HIV test counselling
STAGE 3: LAB INVESTIAGTIONS
1. Bone marrow aspiration
2. Biopsy
3. Bronchoscopy
4. Exploratory laprotomy
STAGE 4: TREATMENT
• Continued observation and
examination
• Therapy based on probability of
various causes of fever in that setting
• Avoid shotgun empirical approach
• Antibiotic??- mask infection
Indication for immediate
empirical therapy
• Vital instability
• Neutropenia
• Nosocomial- if bacteremia, fungemia or
persistently high viral loads are a threat
• Cirrhosis, asplenia, immunosuppressive
drug use, exotic travel, environmental
exposures
• change IV lines(culture), drugs
stopped for 72 hours and empirical
therapy started
• Vancomycin (MRSA) with
piperacilin/tazobactum(broad
spectrum gram negative)
• Granulomatous hepatitis or positive
TST- therapeutic trial for TB upto
6wks
• Glucocorticoids and NSIADS- trial
only after ruling out any infections.
Dramatic response in autoimmune
diseases.
Last resort- if fever continues uptil 6 mnths
Initiation of empirical therapy
• Doesnot mark end of treatment
• Rather it commits physician to more
• Thoughtful
• Reeaxamination and
• Evaluation
HAPPY EARTH DAY
Thank you 

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Pyrexia of unknown origin

  • 2.
  • 3. Regulates normal body temperature Normal Rectal temp. being 97.7-99.5°F Oral temp. being 0.7°F lower than rectal while axillary being 1.2°F lower than rectal. Daily normal variation being 0.5-1°F With evening temperatures being higher than the morning If body temp. exceeds normal variation in an individual, that’s called FEVER
  • 4. Liebermiester’s Rule: With each degree centigrade rise in body temp. , heart rate increase by 8 per min Except in those diseases where relative bradycardia sets in.
  • 5. DEFINITION PETERSDORF AND BEESON 1961 TEMP> 101°F ON SEVERAL OCCASIONS DURATION OF FEVER > 3 WEEKS FAILURE TO REACH DIAGNOSIS DESPITE 1 WEEK OF INPATIENT INV.
  • 6. DURACK & STREET’S CLASSIFICATION CLASSIC PUO • 3 OUTPATIENT VISITS OR 3 DAYS IN HOSPITAL W/O ELUCIDATION OF CAUSE • OR 1 WEEK OF “INTELLIGENT AND INVASIVE” AMBULATORY INV. NOSOCOMIAL PUO •IN HOSPITALISED PATIENTS TEMP> 101°F DEVELOPS ON SEVERAL OCCASIONS WHO IS RECEIVING ACUTE CARE AND WHOM WAS NOT MANIFEST OR INCUBATING AT TIME OF ADMISSION •3 DAYS OF INV. INCLUDING ATLEAST 2 DAYS INCUBATION OF CULTURES NEUTROPENIC PUO •TEMP> 101°F ON SEVERAL OCCASIONS IN PATIENTS WHOSE NEUTROPHIL COUNT IS <500uL(n 2-7x10^3) OR EXPECTED TO FALL WITHIN 1-2 DAYS •NO SPECIFIC CAUSE IDENTIFIED 3 DAYS OF INV. INCLUDING ATLEAST 2 DAYS INCUBATION OF CULTURES HIV- ASSOCIATED PUO • >101°F ON SEVERAL OCCASIONS OVER A PERIOD OF >4 WEEKS FOR OUTPT. OR >3 DAYS FOR INPT. WITH HIV •NO SOURCE REVELAED OVER 3 DAYS INV. INCLUDING 2 DAYS INCUBATION OF CULTURES
  • 7. COMMON CAUSES OF PUO TB being the no. 1 DRUG FEVER
  • 8.
  • 9. INFECTIONS Bacterial Infection: Common etiologies •Chronic sinusitis •Mastoiditis •Salmonellosis •Abscesses(subdiaphragmatic,liver,renal,retroperitoneal, paraspinal) •Chronic prostatitis •Pyelonephritis •Bacterial endocarditis(esp if caused by HACEK group) •Osteomyelitis(esp in cases of implantation of prostheses)
  • 11. •TB meningitis •Spinal TB •Bone and joint TB •Grannulomatous hepatitis •Abdominal TB •Genitourinary TB •Tubercular lymphadenopathy
  • 13.
  • 16. MISCELLANEOUS Hyperthyroidism Phaechromocytoma Metabolic disorders DRUG FEVER: •Antimicrobials(Beta lactum antibiotics) •Cardiovascular (Quinidine) •Antineoplastic •Antiepileptic (phenytoin)
  • 17. A 45 year old man was admitted to the ICU with acute MI, thrombolysed and reperfused, but then went into persistent hypotension following a cardiac arrest. He developed fever on Day 5. Routine blood investigation showed a polymorpho- nuclear leucocytosis. Blood culture was diagnostic. What could it be???
  • 18. NOSOCOMIAL PUO ETIOLOGY Infections Non infectious cause Undiagnosed Others •Accounts for 50% • suspects will be I/V lines, prothesis, septic phlebitis •Focused approach on sites where occult infection may be present eg sinuses of intubated patients. Accounts for 25% •Acalculous cholecystitis •DVT •Pulmonary Embolism Includes drug fever, withdrawal or transfusion rxns or post myocardial infarction syndrome. 20% remains undiagnosed
  • 19. A 14 year old boy was admitted with high grade fever and pallor. On examination no hepatosplenomegaly, lymphadenopathy or bone tenderness were present. The blood counts were as follows: Hb 8gm%, TLC 3800, P8 L86 E4 M2, ESR 20 mm in 1st hr. Platelet count 2.5 lakhs. What could it be???
  • 20. NEUTROPENIC INFECTIONS Patients on chemotherapy or immune deficiencies are more susceptible to: •Oppurtunistic bacterial infections •Fungal infections like candidiasis •Bacteremic infections •Infections involving catheters •Perianal infections Most common etiological agents are: •Aspergillus •Candida •CMV •Herpes simplex
  • 21. HIV – associated PUO HIV Infection as such may be the cause Other secondary causes are: Pulmonary Tuberculosis Pneumocystis Infection Toxoplasmosis Salmonellosis Cryptococciosis Cytomegalovirus infection M. Avium or M. Intracellulare Non-Hodgkin’s Lymphoma Drug induced fever
  • 23. HISTORY TAKING History of present illness 1)Onset : • Acute: Malaria, pyogenic infection • Gradual: TB, typhoid fever 2) Character: high grade- UTI, TB, malaria, drug 3) Pattern: Whether returns to normal or not • Sustained/ persistent: typhoid, drugs
  • 24. •Intermittent fever: Daily spikes: Abscesses, TB, Schistosomiasis Twice – daily spikes: Leishmaniasis •Relapsing/recurrent fever: Non falciparum malaria, Brucellosis, Hodgkin’s 4) Antecedents -Prior to onset of fever: •Dental extraction: infective endocarditis •Urinary catheterization: UTI, bacteremia
  • 25. 5) Associated symptoms: • Rigors and chills  Bacterial, rickettsial and protozoal disease Influenza, lyphoma, leukaemia, drug-induced •Night sweats: TB, Hodgkin’s lymphoma •Loss of weight: malignancy, TB •Cough and dyspnoea: miliary TB, multiple pulm. Emboli, CMV •Headache: Giant cell arteritis •Joint pain: RA,SLE, vasculitis
  • 26. • Abd. Pain – Cholangitis, biliary obstruction, perinephric abscess, Crohn’s disease, dissecting aneuryms, gynaecological infection • Bone pain – Osteomyelitis, lymphoma • Sorethroat – IM, retropharyngeal abscess, post-Streptococcal infection • Dysuria, rectal pain – Prostatic abscess, UTI • Altered bowel habit – IBD, typhoid fever, schistosomiasis, amoebiasis • Skin rash – Gonococcal infection, PAN,NHL, dengue fever
  • 27. • Past Medical History – Malignancy = leukemia, lymphoma, hepatocellular ca – HIV infection – DM – IBD – collagen vascular disease-SLE, RA, giant cell arteritis – TB – Heart disease: valvular heart disease • Past Surgical History – Post splenectomy/ post- transplantation – Prosthetic heart valve – Catheter, AV fistula – Recent surgery/ operation
  • 28. • Drug History – Drug fever occur within 3 months after start of drugs • may cause low grade fever, usually associated with rash • Due to the allergic reaction, direct effect of drug which impair temperature regulation (e.g. phenothiazine) • E.g. Antiarrhythmic drug: procainamide, quinidine; Antimicrobial agent: penicillin, cephalosporin, hydralazine – After fever: may modify clinical pictures, mask certain infection e.g. SBE, antibiotic allergy
  • 29. Family History –Anyone in family has similar problem: TB, familial Mediterranian fever
  • 30. • Social History – Travel • amoebiasis, typhoid fever, malaria, Schistosomiasis – Residental area • malaria, leptospirosis, brucellosis – Occupation • farmers, veterinarian, slaughter-house workers = Brucellosis • workers in the plastic industries = polymer-fume fever
  • 31. –Contact with domestic / wild animal / birds : • Brucellosis, psittacosis (pigeons), Leptospirosis, Q fever, Toxoplasmosis –Diet history • unpasteurized milk/cheese = Brucellosis • poorly cooked pork = Trichinosis –Sexual orientation = HIV, STD, PID –Close contact with TB patients
  • 32. EXAMINATION • General Calm, conscious, oriented to time, place and person Ill/not ill Built/Weight loss (chronic illness) Vitals CLIPJES(Skin rash)
  • 33. HEAD AND NECK • Feel temporal arteries (tender & thicken) • Eyes – iritis/conjuctivitis (ct disease – reiter syndrome) • Jaundice (ascending cholangitis) • Fundi – choroidal tubercle (miliary tb), roth’s spot (ie) and retinal haemorrhage (leukaemia) • Lymphadenopathy
  • 34. FACE AND MOUTH • Butterfly rash • Mucous membranes • Seborrhoic dermatitis (HIV) • Mouth ulcers (SLE) • Buccal candidiasis • Teeth & tonsils infection (abscess) • Parotid enlargement • Ears – otitis media
  • 35. HANDS • Stigmata of Infective Endocarditis • Vasculitis changes • Clubbing • Presence of arthropathy • Raynaud’s phenomenon
  • 36. ARMS • Drug injection sites • Axillary nodes (lymphoma, sarcoidosis, focal infection) • Skin
  • 37. CHEST • Bony tenderness • CVS – murmurs (ie atrial myxoma), rubs (pericarditis) • Resp – signs of pneumonia, TB, empyema and lung ca
  • 38. ABDOMEN • Rose coloured spot (typhoid fever) • Hepatomegaly (hepatic ca, alcoholic hepatitis) • Splenomegaly (haemopoietic malignancy, malaria) • Renal enlargement (renal cell ca) • Testicular enlargement (seminoma) • Penis & scrotum – discharge/rash • Inguinal ligament
  • 39. • Per rectal exam – mass/tenderness in rectum/pelvis (abscess, ca, prostatitis) • Vaginal Examination – collection of pelvic pus/ Pelvic Inflammatory Disease
  • 40. CENTRAL NERVOUS SYSTEM • Signs of meningism (chronic tb meningitis) • Focal neurological signs (brain abscess, mononeuritis multiplex in polyarteritis nodosa)
  • 41. STAGE 1: LAB INVESTIAGTIONS Stage 1: (screening tests) 1. Full blood count (evalute anaemia, +nce of blasts, thrombocytopenia) 2. ESR & CRP 3. LFTs 4. Blood culture 5. Serum virology (EBV,CMV) 6. M/b panel (LFT,LDH,creatinine) 7. Urinalysis and culture 8. Sputum culture and sensitivity 9. Stool and occult blood 10. CXR 11. Mantoux test
  • 42. STAGE 2: LAB INVESTIGATIONS 1. Repeat history and examination 2. Protein electrophoresis 3. CT (chest, abdomen, pelvis) 4. Autoantibody screen (ANA, RF, ANCA, anti-dsDNA) 5. Echocardiography 6. Bone scan(osteomye.) 7. Lumbar puncture 8. Consider PSA, CEA 9. Temporal artery biopsy 10.HIV test counselling
  • 43. STAGE 3: LAB INVESTIAGTIONS 1. Bone marrow aspiration 2. Biopsy 3. Bronchoscopy 4. Exploratory laprotomy
  • 44.
  • 46. • Continued observation and examination • Therapy based on probability of various causes of fever in that setting • Avoid shotgun empirical approach • Antibiotic??- mask infection
  • 47. Indication for immediate empirical therapy • Vital instability • Neutropenia • Nosocomial- if bacteremia, fungemia or persistently high viral loads are a threat • Cirrhosis, asplenia, immunosuppressive drug use, exotic travel, environmental exposures
  • 48. • change IV lines(culture), drugs stopped for 72 hours and empirical therapy started • Vancomycin (MRSA) with piperacilin/tazobactum(broad spectrum gram negative)
  • 49. • Granulomatous hepatitis or positive TST- therapeutic trial for TB upto 6wks • Glucocorticoids and NSIADS- trial only after ruling out any infections. Dramatic response in autoimmune diseases. Last resort- if fever continues uptil 6 mnths
  • 50. Initiation of empirical therapy • Doesnot mark end of treatment • Rather it commits physician to more • Thoughtful • Reeaxamination and • Evaluation
  • 51.