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==Pathophysiology==
==Pathophysiology==

Revision as of 18:33, 27 February 2021

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Zaida Obeidat, M.D.

Synonyms and keywords: Fever in kids

Overview

Historical Perspective

  • The history of fever are briefly reviewed by the Greeks as well as the views brought up in the Bible and widespread throughout the Middle Ages where fever and disease were interpreted as punishment for misbehavior
  • Later views are introduced, based on the rise of science and Harvey's discovery of the circulation of the blood which produced two rival camps, iatrochemists and iatrophysicists.
  • Next are brought up as the contributions of tissue pathology, experiments defining the role of the CNS in regulating body temperature, the old correlation of fever with inflammation and the discovery of microbial agents of disease and bacterial pyrogens in the late nineteenth and early twentieth century
  • Finally, work in the last 30 years is summarized, starting with the discovery of endogenous pyrogen (EP) and the recent finding that EP is probably similar to lymphocyte activating factor (LAF) and leukocytic endogenous mediator (LEM) which collectively as interleukin-1 IL-1 play a major role in both inflammation and immunity.[1]

Classification

  • Fever also can be classified based on height of body temperature into:
  • The height of fever may correlate with severity of illness, such as in dengue fever, shigellosis, and acute falciparum malaria.
  • There are three major fever type: Sustained/continuous fever, intermittent fever and remittent fever.
    • Continuous or sustained fever does not fluctuate more than about 1°C (1.5°F) during 24hours, but never touches normal, characteristics of lobar and gram negative pneumonia, typhoid, acute bacterial meningitis, and urinary tract infection.
    • Fever with bradycardia (Faget’s sign or sphygmothermic dissociation)is characteristic of untreated typhoid, leishmaniasis, brucellosis, Legionnaire’s disease and psittacosis, and Yellow Fever.
    • Intermittent fever is defined as fever present only for several hours during the day. It can be seen in malaria, pyogenic infections, tuberculosis (TB), schistosomiasis, lymphomas, leptospira, borrelia, kala-azar, or septicemia.
    • Sources of continuous, intermittent or transient bacteraemia may lead to continuous, intermittent or transient fevers respectively. Inmalaria, depending on the specie of parasite, fever can occur with a periodicity of 24h (quotidian-due to plasmodium falciparum), 48h (tertian plasmodium ovale and vivax), or 72h (quartan Plasmodium malaria). The Pel-Epstein’s feveris an intermittent low grade fever characterised by3—10 days of fever with subsequent a febrile peri-ods of 3—10 days[31,40]. It is thought to be a typical but rare manifestation of Hodgkin’s lymphoma.
    • Remittent fever is defined as fever with daily fluctuations exceeding 2◦C but at no time touches normal. Remittent fevers are often associated with infectious diseases such as infective endocarditis, rickettsiae infections, and brucellosis. Relapsing fevers refer to those that are recurring and separated by periods with low-grade fever or no fever. Periodic orrelapsing fevers are seen in malaria, lymphoma,borrelia, cyclic neutropenia, and rat-bite fever. Fever associated with night sweats has been described in infectious diseases such as TB, Nocardia, brucellosis, liver or lung abscess and sub-acute infective endocarditis, as well as in non-infectious diseases such as polyarteritis nodosa and cancers such as lymphomas.
Body temperature °C °F
Normal 37-38°C 98.6-100.4°F
Mild/low grade fever 38.1-39°C 100.5-102.2°F
Moderate grade fever 39.1-40°C 102.2-104.0°F
High grade fever 40.1-41.1°C 104.1-106°F
Hyperpyrexia >41.1°C >106.0°F

Pathophysiology

  • The development of the pyrexia is similar to the normal thermoregulatory processes that follow exposure to cold temperatures.[2]
  • The thermal balance point in fever is reset to a higher level such that normal peripheral and central body temperatures are now sensed as cold temperature signals by the thermoregulatory circuitry.
  • Fever is different from heat stroke and hyperthermia where body temperature is increased without an equivalent increase of the thermal balance point.

The role of pyrogens and cryogens

  • The initiation, manifestations and regulation of pyrexia are dependent on the pyrogenic and anti-pyretic properties of numerous exogenous and endogenous substances.
  • Pyrogens directly or indirectly lead to pyrexia and cryogens prevent extortionate temperature elevation.
  • The balance in the interactivity between pyrogens and cyrogens is control the height and duration of the pyrexia.

Pryogens

  • Pyrogens are classified into exogenous and endogenous pyrogens based on their site of production.
  • Exogenous pyrogens are part or whole micro organisms (lipopolysaccharide (LPS) in gram negative cell wall) or products of micro organisms as toxins.
  • Endogenous pyrogens include muramyl dipeptidase and enterotoxins of Staphylococcus aureus and group A and B Streptococcus (superantigens).
  • Endogenous pyrogens are mainly pyrogenic cytokines including interleukins (IL-6, IL-1), interferon gamma (INF-a) and ciliary neurotropic factor(CNTF) and tumor necrosis factor (TNFa).

Cryogens

  • Cyrogens include cytokines(IL10), hormones (a-melanocyte stimulating hormone, corticotrophin and corticotrophin releasing hormone) and neuroendocrine products (neuropeptide Y, bombesin, and thyroliberin), and cytochrome P-450.
  • The antipyretic effect induced by inhibiting synthesis of pyrogenic cytokines (glucocorticoids), cytokine receptors blockade (IL-1 receptor antagonist), and increasing heat loss by enhancing sensitivity of warm sensitive neurons (bombesin).


The pathophysiological mechanisms for the injurious effects of a fever, classified as follows:[3]

  • Direct cellular damage:
    • Membrane, mitochondrial and DNA damage
    • Stimulation of excitotoxic mechanisms
    • Protein denaturation
    • Cell death
  • Local effects:
    • Cytokine stimulation
    • Inflammatory response
    • Vascular stasis
    • Extravasation
    • Oedema
  • Systemic effects:
    • Endotoxaemia
    • Gut bacterial translocation

Causes

Common conditions that can cause fevers include:

Fever in children can sometimes associated with more serious signs and symptoms, such as:

Serious bacterial infections include:

Causes of undiagnosed fever in children include:[4]

  • Infection
    • Viruses
    • Pyogenic Inection
    • Salmonella Infection
    • Brucellosis
    • Tuberculosis
  • Collagen Vascular Diseases
  • Neoplasm

Differential diagnoses for fever in children

Cause Differential Diagnosis
Infectious; Bacterial or mycobacterial Brucellosis, dental abscess, endocarditis, nontuberculous mycobacteria (eg, Mycobacterium chelonae), occult bacterial infection, recurrent bacterial infections, relapsing fever (Borrelia spp other than Borrelia burgdorferi), Yersinia enterocolitica
Parasitic Malaria (eg, Plasmodium vivax, Plasmodium ovale)
Inflammatory or Immunologic Behçet syndrome, inflammatory bowel disease (eg, Crohn disease), hereditary fever syndromes (eg, FMF), juvenile dermatomyositis, PFAPA syndrome, sarcoidosis, systemic lupus erythematosus, systemic juvenile idiopathic arthritis (Still disease), vasculitis (eg, polyarteritis nodosa)
Malignant Leukemia, lymphoma
Other Benign giant lymph node hyperplasia (Castleman disease), CNS abnormalities (eg, hypothalamic dysfunction), drug fever, factitious fever, IgG4-related disease, immunodeficiency syndromes with recurrent infections


  • CNS—central nervous system; FMF—familial Mediterranean fever; IgG4—immunoglobulin G4; PFAPA—periodic fever, aphthous stomatitis, pharyngitis, and adenitis.[5]

Epidemiology and Demographics

  • Following the widespread use of immunizations against Streptococcus pneumoniae and Haemophilus influenzae b, incidence of fever caused by infection due to these organisms has been decreased.
  • Since 1990, rates of invasive Hib infection (including meningitis) in children 5 years and younger have declined by more than 99%.
  • In 2005, the incidence of fever caused by invasive pneumococcal infection in children declined by 77% from 1998.

Age

  • Fever caused by urinary tract infections (UTIs) are the most common source of serious bacterial infection in children younger than 3 months, commonly from E.coli or Klebsiella species.
  • According to a case series, fever caused by pneumonia is the most common serious bacterial infection in children 3 to 36 months of age, followed by UTI.

Natural History, Complications and Prognosis

  • The majority of patients with [disease name] remain asymptomatic for [duration/years].
  • Early clinical features include [manifestation 1], [manifestation 2], and [manifestation 3].
  • If left untreated, [#%] of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
  • Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
  • Prognosis is generally [excellent/good/poor], and the [1/5/10­year mortality/survival rate] of patients with [disease name] is approximately [#%].

Diagnosis

Symptoms

  • Fever is often characterised by:[2]
    • Chills
    • Rigors
    • Sweating
    • Headache
    • Malaise
    • Anorexia

Physical Examination

  • Initial history and physical examination in infants and young children with fever is aim to identify serious illness. Immunocompromised patients (cancer, asplenia, or HIV infection) need more evaluation and treatment.
  • Benign causes of fever such as vaccination in the past 24 hours are reassuring. Teething is rarely associated with a fever of more than 100.4°F
  • A meta-analysis of febrile children older than one month has identified red flags associated with a high likelihood of serious infection.
  • Clinical Red Flags for Serious Infection in Children Older than One Month[6]
  • Global assessments
    • Parental concerns
    • Physician instinct
  • Child behavior
    • Changes in crying pattern
    • Drowsiness
    • Inconsolability
    • Moaning
  • Circulatory/respiratory
    • Crackles
    • Cyanosis
    • Decreased breath sounds
    • Poor peripheral circulation
    • Rapid breathing
    • Shortness of breath
  • Other factors
    • Decreased skin elasticity
    • Hypotension
    • Meningeal irritation
    • Petechial rash
    • Seizures
    • Unconsciousness

Laboratory Findings

  • History and physical examination cannot identify all children with serious bacterial infections, hence sensible use of imaging and laboratory testing is valuable.

Urinalysis and urine culture

  • Urinalysis is a key factor in the evaluation of fever in infancy and early childhood because UTI is a common cause of serious bacterial infection. *Urine sample should be obtained for all children younger than 24 months with unexplained fever. It may be obtained by catheterization or suprapubic aspiration.
  • In children with voluntary urine control, a clean catch method (urination into a specimen container after cleaning the area around the urethra) may be used.
  • Cultures of specimens collected in a urine bag may have an 85 percent false-positive rate, and urine dipstick testing has a 12 percent false-negative rate.
  • All specimens should be sent for formal urinalysis and culture.
  • UTI rates vary with patient sex and age.
  • In the first three months of life, UTIs are more common in boys than in girls, and much more common in uncircumcised boys. After three months of age, UTIs are more common in girls.

Blood cell counts and blood culture

  • White blood cell (WBC) counts and absolute neutrophil counts have been used to point out serious bacterial infection, including occult bacteremia.
  • Blood cell counts have higher value in neonates than in older children.
  • WBC counts lower than 5,000 per mm3 (5 × 109 per L) or more than 15,000 per mm3 (15 × 109 per L) had a PPV of 44% for serious bacterial infection, and an absolute neutrophil count of more than 10,000 per mm3 (10 × 109 per L) had a PPV of 71% according to a study of neonates up to 28 days of age.
  • Current guidelines recommend a complete blood count with differential and blood culture for infants three months or younger with fever.

Stool testing

  • Diarrhea with fever in neonates and young infants submit systemic illness therefore stool culture and fecal WBC counts are supported.

Inflammatory markers

  • The clinical value of C-reactive protein levels in recognizing serious infection in neonates, infants, and young children is being explored.
  • C-reactive protein (CRP) level of 2 mg per dL (19 nmol per L) or greater has better sensitivity, specificity, and predictive value than a WBC count of greater than 15,000 per mm3 or less than 5,000 per mm3.
  • Elevated levels of procalcitonin (another marker of inflammation and bacterial infection) also appear to have better sensitivity, specificity, and predictive value than WBC counts.

Lumbar puncture

  • Vaccination against S. pneumoniae and Hib has greatly reduced the incidence of meningitis limiting the need for lumbar puncture.
  • Fever with clinical signs of meningitis such as nuchal rigidity, petechiae, or abnormal neurologic findings in neonates, infants and young children is indication for lumbar puncture.
  • In children older than 3 months, the test is not suggested unless neurologic signs are present.
  • Two guidelines recommended a lumbar puncture for well-appearing, previously healthy young infants with no focal signs of infection, a WBC count between 5,000 and 15,000 per mm3, and no pyuria or bacteriuria on urinalysis.
  • Although low peripheral WBC counts (less than 5,000 per mm3) are more often associated with meningitis than with bacteremia, WBC counts should not be used alone to determine which infants need lumbar puncture.

Electrocardiogram

There are no ECG findings associated with fever in children.

X-ray

  • Chest X ray is recommended in all neonates with unexplained fever.
  • Chest X ray is also recommended for young children older than one month revealing respiratory symptoms and for patients with a fever of more than 102.2°F (39°C) and a WBC count of more than 20,000 per mm3 (20 × 109 per L).

Echocardiography or Ultrasound

There are no echocardiography/ultrasound findings associated with fever in children.

CT scan

There are no CT scan findings associated with fever in children.

MRI

There are no MRI findings associated with fever in children.

Treatment

Medical Therapy

  • Fever plays a physiologic role in response to infection, inhibiting bacterial growth and viral replication, and enhancing the immune response.
  • There is no evidence that use of antipyretics prolongs illness in children
  • Antipyretic treatment should be reserved for distressed children, aiming at improving the child’s wellbeing rather than achieving normothermia.
  • Antipyretic treatment has not been shown to prevent recurrence of febrile seizures.
  • Response to antipyretics cannot predict the severity of the underlying illness, since children with bacterial and viral illnesses have a similar response to antipyretics [134]. However, evaluating if the child’s conditions markedly improve with antipyretic treatment may be useful to discern whether it was related to fever or to the severity of the underlying illness.
  • In children with inherited metabolic and mitochondrial diseases, catabolic stressors should be avoided, and both fever and underlying infections should be treated
  • Fever may increase metabolic and oxygen consumption; therefore, aggressive treatment may be more important in children with a limited cardiopulmonary or metabolic reserve, and it is recommended in patients recovering from cardiac arrest.
  • Ibuprofen and acetaminophen are the only drugs approved for treatment of fever in children and they are generally considered to be equally safe and effective for reducing temperature and relieving discomfort.
  • Combination therapy with acetaminophen plus ibuprofen seems to be slightly more effective in reducing body temperature compared with monotherapy alone[7]

References

  1. Stein MT (1991). "Historical perspective on fever and thermometry". Clin Pediatr (Phila). 30 (4 Suppl): 5–7. doi:10.1177/0009922891030004S02. PMID 2029820.
  2. 2.0 2.1 2.2 Ogoina D (2011). "Fever, fever patterns and diseases called 'fever'--a review". J Infect Public Health. 4 (3): 108–24. doi:10.1016/j.jiph.2011.05.002. PMID 21843857.
  3. Walter EJ, Hanna-Jumma S, Carraretto M, Forni L (2016). "The pathophysiological basis and consequences of fever". Crit Care. 20 (1): 200. doi:10.1186/s13054-016-1375-5. PMC 4944485. PMID 27411542.
  4. BREWIS EG (1965). "CHILD CARE IN GENERAL PRACTICE. UNDIAGNOSED FEVER". Br Med J. 1 (5427): 107–9. PMC 2165027. PMID 14218464.
  5. Soon GS, Laxer RM (2017). "Approach to recurrent fever in childhood". Can Fam Physician. 63 (10): 756–762. PMC 5638471. PMID 29025800.
  6. Van den Bruel A, Haj-Hassan T, Thompson M, Buntinx F, Mant D, European Research Network on Recognising Serious Infection investigators (2010). "Diagnostic value of clinical features at presentation to identify serious infection in children in developed countries: a systematic review". Lancet. 375 (9717): 834–45. doi:10.1016/S0140-6736(09)62000-6. PMID 20132979.
  7. Barbi E, Marzuillo P, Neri E, Naviglio S, Krauss BS (2017). "Fever in Children: Pearls and Pitfalls". Children (Basel). 4 (9). doi:10.3390/children4090081. PMC 5615271. PMID 28862659.