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FUO Basics Patty W. Wright, MD & C. Buddy Creech, MD, MPH with appreciation to William Goins, MD and Bryan Youree, MD March 2011 Objectives To discuss the definition of fever of unknown origin (FUO) the classifications of FUO the most common etiologies of FUO the diagnostic work-up of patients with FUO What is a normal body temperature? Normal Body Temperature (Adults) 1 million axillary temperatures measured twice daily in 25,000 healthy adults Mean temperature: 37°C (36.2 – 37.5°C) Readings >38.0°C were deemed as “suspicious/probably febrile” Thermometers may have read 1.4 – 2.2°C (2.6 – 4.0°F) higher than today’s instruments Wunderlich C. Das Verhalten der Eigenwärme in Krankenheiten. Leipzig, Germany: Otto Wigard;1868. Mackowiak, et al., JAMA 1992;268:1578 Normal Body Temperature (Adults) Patients 148 healthy adults Method Oral temp with electronic thermometer Frequency 1 – 4 times daily for 3 days Mean 36.8 ± 0.4°C (98.2 ± 0.7°F) Upper limits of normal 37.2°C (98.9°F) in the early morning 37.7°C (99.9°F) overall Mackowiak, et al., JAMA 1992;268:1578 Normal Body Temperature (Adults) Mean temperature varied diurnally Low: 6 AM Peak: 4 – 6 PM Mean variability: 0.5°C (0.9°F) Women had slightly higher temperatures Black subjects tended to have higher temperatures than whites Mackowiak, et al., JAMA 1992;268:1578 Normal Temperature Curves (Children) What is hyperthermia? Hyperthermia Unregulated elevation of temperature Does not involve hypothalamic thermoregulatory center Cytokines not directly involved Mechanisms of Hyperthermia 1. • • • • • • 2. Disorders of heat Excessive heat dissipation production • Heat stroke Exertional • Autonomic hyperthermia dysfunction Thyrotoxicosis Pheochromocytoma 3. Disorders of Cocaine hypothalamic function Delerium tremens • Neuroleptic Malignant malignant syndrome hyperthermia • CVA • Trauma What is fever? Fever Resetting of the thermostatic set-point in the anterior hypothalamus Initiation of heat-conserving mechanisms Cytokine-mediated What is a Fever of Unknown Origin? Fever of Unknown Origin Temp > 101°F (38.3°C) on several occasions Fever of at least 3 weeks duration No diagnosis after a 1 week evaluation in the hospital or (in the modern era) a reasonable outpatient work-up Petersdorf RG, Beeson PB. Medicine 1961;40:1-30. Historical Causes of FUO Hippocrates: Excess of yellow bile Middle Ages: Demonic possession (encephalitis?) 18th Century: Friction associated with the flow of blood through the vascular system and from fermentation and putrefaction occurring in the blood and intestines Categories of FUO Feature Nosocomial Neutropenic HIVassociated Patient’s situation Hospitalized, acute care, no infection when admitted Neutrophil Confirmed count <500/µL HIV-positive or expected to reach that level in 1-2 days Duration of illness 3 days b 3 days b Classic All others with fevers for ≥3 weeks 3 days b 3 days b or 3 outpatient (or 4 weeks as outpatient) visits require temperatures of ≥38.3°C (101°F) on several occasions. bIncludes at least 2 days’ incubation of microbiology cultures. aAll Modified from DT Durack, AC Street, in JS Remington, MN Swartz (eds): Current Clinical Topics in Infectious Diseases. Cambridge, MA, Blackwell, 1991. What are the three most common causes of FUO (in general)? Classifications of FUO Modified from DT Durack in Mandell, Bennett, and Dolin. Principles and Practice of Infectious Diseases, 2005. 6th ed. Evolving Etiology of FUO in Adults Mourad, et al. Arch Intern Med. 2003;163:545 Magnitude of Fever 102°F rule Most noninfectious disorders in adults are associated with temperatures ≤ 102°F Best used to exclude noninfectious causes of fever 106°F Temperatures ≥ 106°F are rarely due to infection Examples: central fever, drug fever, NMS, malignant hyperthermia Causes of FUO in Adults Type Infections Common TB Extrapulmonary Renal Meningitis Miliary Intra-abdominal abscess Liver Splenic Pancreatic Perinephric Psoas Placental Pelvic abscess Uncommon SBE CMV Toxo Salmonella enteric fever Intra/perinephric abscess Splenic abscess Rare Dental abscess Brain abscess Vertebral osteo Listeria Yersinia Brucellosis Relapsing Fever Rat-bite fever Chronic Q fever Cat-scratch fever HIV EBV Malaria Whipple’s disease Cunha BA. Fever of unknown origin. Infect Dis Clin North Am 1996;10:111-127. What is the most common malignancy causing FUO? Causes of FUO Type Common Malignancy Lymphoma Liver/CNS mets Hypernephromas Uncommon Hepatomas Pancreatic CA Preleukemias Colon CA Rare Atrial myxomas CNS tumors Myelodysplastic diseases Cunha BA. Fever of unknown origin. Infect Dis Clin North Am 1996;10:111-127. Causes of FUO Type Common Rheumatologic Still’s disease Temporal Arteritis Uncommon PAN RA Rare SLE Vasculitis Felty’s syndrome ARF Behcet’s disease FMF Cryoglobulinemia Reiter’s syndrome Rheumatic fever Wegener’s disease Sarcoidosis Cunha BA. Fever of unknown origin. Infect Dis Clin North Am 1996;10:111-127. Causes of FUO Type Misc Common Drug Fever Cirrhosis Alcoholic hepatitis Uncommon Granulomatous hepatitis Cerebrovascular accident Rare Hyperthyroidism Addison’s disease PE/DVT Kikuchi’s disease Hyper IgD syndrome Crohn’s disease Ulcerative colitis Cunha BA. Fever of unknown origin. Infect Dis Clin North Am 1996;10:111-127. Drug Fever Diagnosis of exclusion Approximately 10% of fevers in hospitalized patients Look “well” Relative bradycardia may occur Usually no rash Fever usually returns to normal within 3 days May take longer if accompanied by a rash ***************************************** Johnson DH, Cunha BA. Drug fever. Infect Dis Clin North Am 1996;10:85-91. Causes of FUO in Children Series Cases Infxn CVD Neoplasm Misc Undiagnosed McClung (60’s) 99 29% 11% 8% 19% 32% Pizzo (70’s) 100 52% 20% 6% 10% 12% Steele (80’s) 109 22% 6% 2% 3% 67% Chantada (80’s) 113 36% 13% 10% 22% 19% Muoaket (80's) 221 78% 5% 2% - 15% Most common infectious etiologies in children: Bartonella, EBV, CMV, Histoplasmosis, Blastomycosis, TB What is periodic fever? Periodic Fever Periodic is different from sporadic, intermittent, occasional Periodicity involves having repeated cycles appearing at regular intervals Periodic Fever Syndromes Non-familial PFAPA (Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis) Familial Familial Mediterranean Fever (FMF) Hyper IgD Syndrome (HIDS) TNF-receptor associated periodic syndrome (TRAPS or Hibernian Fever) Muckle-Wells Syndrome (MWS) Familial Cold Urticaria (FCU) Cyclic Hematopoesis (CH) PFAPA Case Definition Periodic fevers beginning before the age of 5 years At least one clinical criterion (ulcers, pharyngitis, adenitis) Absence of cough, purulent rhinitis, or otitis on examination Asymptomatic periods between attacks Normal growth and development Exclusion of cyclic neutropenia PFAPA Registry (Vanderbilt) In 1997, parents of registry patients were contacted by telephone to collect information on patients believed by their physicians to have PFAPA 94 patients were available, 83 with long-term follow-up data Characteristics of PFAPA Patients Original Registry Follow-up Number of Patients 94 83 Female 42 36 Male 52 47 Onset of PFAPA 2.8 years - Duration of each episode 4.8 days 4.2 days Episodes per year 11.5 10.0 Symptom-free Interval 28.2 days 41.2 days ** Thomas KT, et al. J Pediatr. 1999;135:15-21. PFAPA Symptoms, by Report Original Registry (66) Follow-up (82) Aphthous Ulcers 67% 70% Pharyngitis 65% 72% Lymphadenopathy 77% 88% Chills 80% 80% Cough 20% 13% Coryza 18% 15% Headache 65% 60% Abdominal pain 45% 49% Rash 15% 9% Thomas KT, et al. J Pediatr. 1999;135:15-21. Efficacy of Treatment Treatment No. of Episode s Not Effective Somewhat Effective Moderately Effective Very Effective Acetaminophen 80 55% 26% 15% 6% Ibuprofen 67 15% 31% 21% 33% Antibiotics 71 92% 6% 0% 3% Prednisone 49 10% 4% 10% 76% Cimetidine 28 57% 4% 11% 29% Tonsillectomy 4 25% 0% 25% 50% T&A 47 14% 14% 0% 72% Thomas KT, et al. J Pediatr. 1999;135:15-21. Familial Periodic Fever Syndromes FMF TRAPS HIDS MWS/FCU CH Duration of Attack 1-3 days Days-weeks 3-7 days Days-weeks 4-7 days Clinical Features Serositis; Conjunctivitis, Cervical scrotal pain myalgias adenitis, vomiting Urticaria, deafness, cold intolerance Aphthous stomatitis, adenitis Skin Erysipelaslike lesions Tender red plaques Maculopapular rash Urticaria Furuncles Amyloidosis Frequent Variable Low risk Very Frequent Unknown Inheritance AR AD AR AD AD Ancestry Jewish, Turkish, Armenian Scottish/Irish Dutch, French German, English, French None What is the diagnostic work up for FUO? Diagnostic Testing for FUO in Children First tier Second tier CBC, CMP, blood/urine cultures, ESR/CRP, EBV, CMV, CSD serology, TST Fungal serology; CT chest, abdomen, pelvis with contrast Third tier Gallium or Indium scan; bone scan ***************************************** Diagnostic Algorithm for FUO in Adults Complete History and Physical Assessment Positive Findings Yes Order appropriate and specific diagnostic testing No CBC w/ diff, chemistries, LFTs, blood cultures x3, UA, urine culture, ESR, CRP, ANA, RF, HIV ab, PPD, CXR Positive Results No Yes Order appropriate follow-up diagnostic testing CT of chest/abdomen/pelvis with contrast Adapted from Roth AR, Basello GM. Approach to the Adult Patient with fever of unknown origin. Am Fam Physician. 2003;68:2223-8. Additional Workup for FUO in Adults If symptoms of “mono” syndrome CMV antibodies EBV antibodies HIV viral load Toxoplasmosis serologies If exposure risk factors Q-fever serology If abnormal liver enzyme test results Viral hepatitis serologies Mourad, et al. Arch Intern Med. 2003;163:545 Diagnostic Algorithm for FUO in Adults Assign to most likely category Infection Urine & sputum cultures for AFB, VDRL, HIV test, CMV & EBV serology Malignancies Hematologic Nonhematologic Autoimmune Miscellaneous RF, ANA Order appropriate diagnostic tests based on information from history Mammography, Chest Peripheral CT with contrast, smear, SPEP Upper/lower endoscopy, bone scan, gallium scan No Dx? No Dx? No Dx? No Dx? TTE/TEE, LP, gallium scan, sinus films BM biopsy Brain MRI; Biopsy of LN, skin lesions, or liver TA biopsy, LN biopsy Roth AR, Basello GM. Approach to the Adult Patient with fever of unknown origin. Am Fam Physician. 2003;68:2223-8. Liver Biopsy & Bone Marrow Biopsy Diagnostic yield of liver biopsy 14% 17% Hepatomegaly on exam or abnormal LFT’s not helpful in predicting abnormal biopsy result Complication rate 0.06% - 0.32% Mourand et al. Arch Intern Med 2003;163:545 Diagnostic yield of bone marrow cultures in immunocompetent individuals 0% - 2% Volk et al. J Clin Pathol 1998;110:150 Riley et al. J Clin Pathol 1995:48:706 FUO Prognosis Determined primarily by the underlying disease Outcome worst for neoplasms If undiagnosed after extensive evaluation, adults generally have favorable outcome and fever usually resolves after 4-5 weeks Larson et al. Medicine 1982;61:269 Where is the world’s tallest thermometer? WORLD'S TALLEST THERMOMETER BAKER, CALIFORNIA ***************************************** Case Presentation- “Connor” Connor is an 18 month old male with a one year history of periodic fevers to 104. Between each ‘episode’ the child has grown well and has appeared healthy and active Occasionally there are uncomplicated URI’s and gastroenteritis, but these episodes seem ‘different.’ What additional information would you like to obtain from Connor’s parents? Case Presentation- “Connor” During each episode, his parents report that he has pharyngitis and aphthous ulcers in the mouth. What disease do you think Connor has and how would treat him? PFAPA Treatment is with prednisone 2mg/kg as a single dose at the beginning of each episode. Rarely, children will require a second dose 24 hrs later. Treatment typically results in immediate resolution of fever and other symptoms. Primary side effect of treatment is shortening of the interval between episodes. PFAPA typically spontaneously resolves prior to adolescence. Case Presentation- “Kyle” Kyle is a 7 year old male with daily fever to 103 for 3 weeks and a 10-pound weight loss. He denies other symptoms. He reports no unusual exposures or travel. He attends 2nd grade. On examination, his temperature is 104. There are no focal findings, though there is a hint of abdominal discomfort. How would you proceed with his work-up? Case Presentation- “Kyle” CBC WNL. EBV and CMV titers c/w past infection. ALT 60. AST 36. ESR 52. CRP 9 (nml < 10). Abdominal ultrasound normal. What additional work up would you consider at this time? Cat Scratch Disease Abdominal CT confirmed small microabscesses in the spleen and liver Bartonella serologies revealed an IgG>1:512 consistent with diagnosis of disseminated CSD Additional history revealed that the patient’s family bought a new kitten about 1 month prior to presentation. Cat Scratch Disease Treatment not recommended for otherwise uncomplicated CSD in kids Treatment with azithromycin is recommended for patients who are immunocompromised May consider treatment for disseminated disease While a h/o scratches and local skin eruption/LAD are common, they are not universal. ***************************************** Case Presentation- “Bill” Bill is a 74 year old male with CAD and HTN who present to the clinic c/o fever. He reports fevers to 101.7 over the past week. He reports associated fever and malaise. He denies associated GI, GU, or URI symptoms. This is his first health care visit for his fevers. Does Bill have an FUO? Case Presentation - “Bill” Bill has fever (T>101), but the duration is < 3 wks, and he has not had an evaluation. Bill has a fever of unknown etiology, but not an FUO. Case Presentation - “Bill” Bill’s physical exam is negative. Bill has a CBC with diff which shows a mild anemia. U/A was negative. Chemistries and LFT’s were WNL. Bill is advised that he likely has a viral infection and is prescribed acetaminophen, po fluids, and rest. Bill returns to the clinic 1 week later with continued fevers. What additional history should be obtained? Case Presentation- “Bill” Additional history… Travel history, recent & any h/o international travel Animal exposures Sick contacts Family history of fevers Medications, including herbals & OTC meds Bill denies any travel, animal or sick contact exposure, or FH of fevers. His meds are stable and include ASA, a beta-blocker, & a statin. Case Presentation- “Bill” Bill’s physical exam remains negative. He has additional lab studies including blood and urine cultures, ANA, RF, and HIV ab, all of which are negative. Chest x-ray shows no acute disease. PPD is negative. ESR is elevated at 126 (normal < 20). CRP is 153 (normal < 10). What disease do you think Bill has, and how would you diagnose it? Case Presentation- “Bill” Temporal arteritis May present with only fever and fatigue May have associated HA, jaw claudication, or visual changes May note nodules or diminished temporal artery pulsations on exam ESR typically > 50 mm/hr and often > 100 mm/hr Dx with temporal artery biopsy May need removal of extensive segments as can have patchy involvement of the artery Rx with steroids Temporal Arteritis (Giant Cell Arteritis) www.neuropathologyweb.org Case Presentation- “Sara” Sara is a 30 year old female graduate student who presents to your office with fevers to 101.5 for the past month. She reports associated flank pain and dysuria without N/V/D. Exam was negative. She has been previously evaluated in the student health clinic on 3 occasions. On her first visit, she was noted to have a U/A positive for leukocyte esterase with a negative urine culture. She was given trim-sulfa x 3 days without improvement. Case Presentation- “Sara” On her second visit, she had a repeat U/A with micro which showed 10-20 WBC with a negative urine cx. She was treated with levofloxacin x 14 days. Her fevers improved while on abx; however, they returned after her abx were d/c’ed. On her third visit, a CBC w/ diff showed a mild leukocytosis. Her chemistries and LFT’s were WNL. KUB was negative. U/A again had + WBC, so she was treated empirically with metronidazole without relief. Case Presentation- “Sara” Does Sara have an FUO? What additional history would you like to obtain? Case Presentation- “Sara” Sara has had fevers > 101 for > 3 wks and has undergone a basic work-up. She meets the definition of FUO. Additional history… Travel history, recent & any h/o international travel Animal exposures Sick contacts Family history of fevers Sexual history Case Presentation- “Sara” Sara reports that she grew up in South Africa and came to the US at 18 years of age to attend college. She has a pet iguana. She denies sick contacts w/ similar symptoms. No family history of fevers. She is sexually active with her boyfriend of 6 months. He is her second life-time sexual partner. What additional studies would you obtain at this time? Case Presentation- “Sara” Additional studies… Gyn exam with STD screening, including tests for GC, chlamydia, HIV, and trichomonas CT of abdomen and pelvis Blood cultures You also recommend a PPD, but Sara states that she had BCG vaccination as a child. Do you proceed with PPD testing? Case Presentation- “Sara” Yes. In the US, we ignore prior BCG vaccination status when interpreting PPD results (i.e. a positive is still a positive regardless of prior vaccination). www.stanford.edu Case Presentation- “Sara” Sara’s gyn exam and STD screen are negative. Her CT shows scarring of the right kidney. She returns at 48 hrs to have her PPD read. She has 12 mm of induration. Does Sara have a positive or negative PPD? Case Presentation- “Sara” Patient Status Positive Result HIV + >5mm Healthy individuals with exposure history or risk factors >10mm Healthy individuals with no exposure history >15mm www.stanford.edu Case Presentation- “Sara” What disease do you think Sara has, and how would you diagnose it? www.cdc.gov Case Presentation- “Sara” Renal Tuberculosis Culture of 3 morning urine specimens for mycobacteria establishes the diagnosis in 80% to 90% of cases Urine TB PCR has a sensitivity of 87100% and specificity of 92-99.8% Renal TB www.vetmed.wsu.edu Summary FUO is often a diagnostic dilemma Infections, inflammatory disorders, and malignancy account for the majority of cases Diagnostic approach should occur in a stepwise fashion based on the H&P Up to 30% of FUO’s in the modern era are undiagnosed Patients that remain undiagnosed generally have a good prognosis What are your questions?