Enteric fever in children

Enteric fever. typhoid fever. in children. medical management.

1. Enteric Fever Presented by Dr. Ankit Agarwal Guided by: Dr. B.S. Natani Dept. of Pediatrics NIMS, Jaipur

2. Overview History Epidemiology Etiology Pathogenesis Clinical Features Complications Diagnosis Differential Diagnosis Treatment Prevention and Vaccination References

3. History Thomas Willis : In 1659 credited with the first description of Typhoid fever Evidence of cases of Typhoid Fever dates back to 430 BC, when a devastating illness killed one-third of the population of Athens. In 2006, a study detected DNA sequences similar to Salmonella in dental pulp extracted from a burial pit dated to the time of the outbreak. Until the nineteenth century Typhoid Fever and Typhus were considered the same. John Huxam in 1739 first described the difference between the two. Thomas Willis

4. In 1880, Karl Joseph Eberth described a typhoid bacillus. In 1884, pathologist Georg Theodor August Gaffky confirmed Eberth's findings, and the organism was given names such as Eberth's bacillus, Eberthella typhi , and Gaffky -Eberth bacillus . French physician Pierre Charles Alexandre Louis in 1829 first proposed the name “ T yphoid Fever ”-meaning to resemble typhus. In 1837 William Wood Gerhard was the first to differentiate clearly between typhus fever and typhoid William Budd in 1856 described the feco -oral method of transmission of Typhoid fever Pierre Charles Alexandre Louis Karl Joseph Eberth

5. Georges-Fernand- Isidor Widal In 1896 Georges-Fernand- Isidor Widal described the ‘ Widal agglutination reaction’ and called it “ Sero -Diagnosis” In the same year Sir Almroth Edward Wright developed an injectable heat killed whole cell vaccine for Typhoid. S. Paratyphi isolated in 1902 by H. Kayser Mary Mallon, also known as Typhoid Mary . In 1907, she became the first American carrier to be identified and traced. She was a cook in New York and was associated with 53 cases and 3 deaths. Health authorities told Mary to give up working as a cook or have her gall bladder removed. She was detained and quarantined after another typhoid outbreak. She died of pneumonia after 26 years in quarantine.

6. Epidemiology Over 21.6 million cases of Typhoid annually worldwide Over 2,00,000 deaths annually due to Typhoid Additional 5.4 million cases of Paratyphoid annually Indian subcontinent has the highest incidence of the disease worldwide. Enteric Fever is endemic in India In India the incidence is 214.2/1,00,000/ yr Age-Specific studies show that incidence in younger children are higher (0-4y:2,730; 5-19y:1,170; 20-40y:110 /1,00,000 per year)

7. Enteric Fever is a collective term used for Typhoid and Paratyphoid fevers.

8. Typhoid fever is caused by Samonella e nterica sub-species  enterica serovar Typhi ( S. Typhi ) Paratyphoid fever is caused by Samonella enterica sub-species  enterica serovar Paratyphi A , Paratyphi B (also called S. schottmuelleri ), Paratyphi C (also called S. hirschfeldii ) Belong to Enterobacteriaceae   family Gram Negetive , Rod-shaped , non-spore-forming , predominantly motile bacteria with and peritrichous  flagella   A re   chemoorganotrophs and facultative anaerobes .   Etiology

9. Antigenic Structure Salmonella posses following antigens on which they are classified and identified: Flagellar or H Antigen : present on the flagella and is dual core heat labile protein. Strongly Immunogenic. Agglutinate rapidly with antisera. (Large, loose, fluffy clumps) Somatic or O Antigen : phospholipid-protein-polysaccharide complex. Integral part of cell wall. Endotoxin. Heat Stable. Slow agglutination with antisera (Compact, chalky, granular clumps) Surface, Capsule or Vi Antigen : surface polysaccharide antigen enveloping O antigen. Heat labile. Act as Vi rulence factor. Poorly immunogenic

10. Gram Staining of S. Typhi S. Typhi showing peritrichous  flagella

11. Pathogenesis Humans are the only reservoir of S. Typhi and S. Paratyphi A. S. Paratyphi B, and S. Paratyphi C also infect dogs, cattle and poultry and can also transmit by eggs or poorly cooked meat. Mode of Transmission : Feco -Oral Route (Most Common). Less commonly urine of infected person. Infectious Dose : 10 5 – 10 9 organisms. Incubation Period : usually 7 – 14 days (can be upto 3 – 30 days depending upon the infecting dose)

12. Ingestion of contaminated food or water S . typhi reaches terminal ileum and invades gut mucosa through specialized antigen-sampling cells known as M cells (Microform cells ). Within the Peyer patches in the terminal ileum. S. t yphi is phagocytosed by macrophages. These macrophages then enter the mesenteric lymphoid system and then pass into the blood stream via the lymphatics. These bacteria are disseminated throughout the body and colonize the organs of the reticuloendothelial system T hey replicate within macrophages and are shed back into the blood, causing a secondary bacteremia.

13. The surface Vi polysaccharide capsular antigen found in S. Typhi interferes with phagocytosis and an virulence trait encoded by the PhoP regulon gives ability to survive within macrophages after phagocytosis S. typhi avoids triggering of an early inflammatory response in the gut and instead colonize deeper tissues and organ systems. Produces an inflammatory response in the deeper mucosal layers and underlying lymphoid tissue causing hyperplasia of Peyer patches and subsequent necrosis and sloughing of overlying epithelium.

14. These ulcers can bleed but usually heal without scarring or stricture formation. Inflammatory lesion may occasionally penetrate the muscularis and serosa of the intestine and produce perforation. The mesenteric lymph nodes, liver, and spleen are hyperemic and generally have areas of focal necrosis as well. A mononuclear response may be seen in the bone marrow in association with areas of focal necrosis.

15. Carriers The propensity to become a carrier follows the epidemiology of gallbladder disease. Increasing with patient age and the antibiotic resistance of the prevalent strains. Carriage are generally lower in children than adults . Types of Carriers: Convalescent carrier : passes bacilli in the excreta form 3weeks-3months after clinical cure of typhoid. Temporary carrier: passes bacilli in the excreta form 3months-1year after clinical cure of typhoid Chronic faecal carrier: continues to pass bacilli intermittently in the excreta at least one year after infection . Chronic urinary carrier: the renal pelvis is infected & bacilli pass in urine

16. Clinical Features Mean age of onset in India is 10yrs. Onset is insidious and varies from a mild illness with low-grade fever, malaise , and slight, dry cough to a severe clinical picture with abdominal discomfort and multiple complications P resentation of typhoid may be more dramatic in children younger than 5 yrs of age, with comparatively higher rates of complications and hospitalization .

17. Features of 1 st week of illness Rising Step ladder type of fever, with chills but rigors are rare Relative Bradycardia Dull, expressionless and toxic facies Dry skin with little sweating Coated tongue Musty, damp hay-like/baked bread like odour Vomiting Tender, doughy abdomen with slight guarding Constipation / Diarrhea (Pea Soup diarrhea) Occasionally minimal, non-productive cough Meningismus may occur early.

18. Dull, expressionless and toxic facies Coated Tongue Pea Soup Stools

19. Features of 2 nd week of illness Continuous High grade fever (39.5-40.5 C) Worsening of cough may occur Rose Spots Abdominal Pain and tenderness Soft tender splenomegaly Soft tender hepatomegaly

20. Rose Spots F aint salmon coloured macules on the trunk and abdomen Appear in crops of 10-15 First seen after 7-10 days of illness Last for upto 2-3 days Fades on pressure Difficult to see in dark-skinned children .

21. Features of 3 rd week of illness Hepatosplenomegaly Intestinal bleeding or perforation Features of peritonitis Septic Shock Altered Sensorium In absence of acute complications or death, symptoms gradually resolve over 2-4 weeks, however, the illness may be associated with malnutrition in a number of affected children

22. Enteric fever caused by S. Paratyphi organisms classically have a milder course . However, there have been several outbreaks of infection with drug-resistant S. paratyphi A , suggesting that paratyphoid fever may also be severe, with significant morbidity and complications

23. Complications Gastrointestinal Intestinal haemorrhage , perforation Central nervous system Encephalopathy, cerebral edema, subdural empyema, cerebral abscess, meningitis, ventriculitis , transient parkinsonism, motor neuron disorders, ataxia, seizures, Guillain-Barré syndrome, psychosis, optic neuritis Hepatobiliary system Cholecystitis , hepatitis, hepatic abscesses, splenic abscess, peritonitis, paralytic ileus, acute pancreatitis, splenic rupture

24. Pulmonary system Pneumonia, empyema, bronchopleural fistula, Bronchitis, pleural effusion, pneumothorax Cardiovascular system Endocarditis, myocarditis, pericarditis, arteritis, congestive heart failure, shock Musculoskeletal System Osteomyelitis, septic arthritis, Periostitis , typhoid spine, muscular rupture, Psoas abscess, gluteal abscess, cutaneous vasculitis

25. Genitourinary system Urinary tract infection, renal abscess, pelvic infections, testicular abscess, prostatitis, epididymitis, Glomerulonephritis, pyelonephritis, cystitis Haemopoeitic Haemolysis , DIC, Hemophagocytosis syndrome Others Bed sores, hypercalcaemia , decubitus ulceration, abortion

26. Diagnosis Bacteriological diagnosis of enteric fever consists of: Isolation of the bacilli from patient (Culture) Demonstration of antibodies in serum (Serological) Demonstration of typhoid antigen in serum or urine (Serological)

27. Blood Culture Bacteremia occurs early in the disease Blood culture is positive in about 90% cases in 1 st week 75% cases in 2 nd week 60% cases in 3 rd week 25% thereafter till subsidence of pyrexia Blood cultures rapidly becomes negative on treatment with antibiotics. Isolation of the bacilli from patient

28. Method of Blood Culture 5-10 ml of blood is collected and inoculated into a culture bottle containing 50-100 ml of 0.5% bile broth. After incubation overnight at 37 o C , the bile broth is sub cultured on MacConkey agar. Pale, non-lactose fermenting colonies that grow are further subjected to biochemical tests. Salmonella will be motile , indole and urease negative and ferment glucose, mannitol and maltose but not lactose or sucrose. Typhoid bacillus will be anaerogenic while Paratyphoid bacilli will form acid and gas from sugar. Further confirmation is done by slide agglutination of the colonies Cultures should be declared negative only after the broth is sub cultured every day for ten days.

29. MacConkey agar with LF and non-LF colonies

30. S. Typhi Does not fermet sugar to produce acid and gas S.Paratyphi Fermet sugar to produce acid and gas

31. Other samples which can be cultured Bone Marrow Blood Clot Feces Urine Bile CSF Pus from suppurative lesions Sputum Rose Spots

32. Wilson Blair Bismuth Sulphate Agar. Selective for S. Typhi

33. Demonstration of antibodies in serum Widal Test This is a test for the measurement of H and O agglutinins for typhoid and paratyphoid bacilli in the patients sera. The antigens used in the test are the H and O antigens of S. typhi and H antigens of S. paratyphi A and B. Readymade Widal kits of stained antigen are now available commercially for use

34. Interpreting the Widal Test The agglutination titre will depend upon the stage of the disease. Agglutinins usually appear by the end of the first week and increases steadily till the third or the fourth week, after which it declines gradually. Demonstrating of a rise in titre of antibodies, by testing two or more serum samples, is more meaningful than a single test. The result of a single test should be interpreted with caution. It is difficult to lay down levels of significance though it is generally stated that titres of 1/100 or more of O agglutinins and 1/200 or more for H agglutinins are significant.

35. Agglutinins may be present on account of prior disease, inapparent infection or immunization. Therefore the mere presence of agglutinin in the Widal test should not be taken as proof of typhoid fever Persons who have had a prior infection or immunization may develop an anamnestic response during an unrelated fever. This may be differentiated by repetition of the test after a week. The anamnestic response shows only a transient rise, while in entric fever the rise is sustained. Bacterial suspensions used as antigens should be free form fimbria. False positive results may otherwise occur. Cases treated early with chloramphenicol may show a poor agglutinin response.

36. Other test to detect circulating antibodies: ELISA – e.g. Typhidot Typhidot consists of a dot ELISA kit that detects IgM and IgG antibodies against the outer membrane protein of S. typhi . The typhidot test becomes positive within 2–3 days of infection and separately identifies IgM and IgG antibodies. The most important limitation of this test is that it is not quantitative and result is only positive or negative . Counterimmunoelectrophoresis (CIE) Indirect Hemeagglutination

37. Demonstration of antigen in serum/urine Sensitized Staphylococcal coagglutination test. PCR Other investigations Results of other laboratory investigations are nonspecific. CBC: Leukocytopenia in relation to the fever and toxicity. In younger children leukocytosis is common and may reach 20,000-25,000 cells/ μL . Thrombocytopenia: may be a marker of severe illness and may accompany disseminated intravascular coagulopathy Liver function test results may be deranged, but significant hepatic dysfunction is rare .

38. Differential Diagnosis Other Salmonella Infection GIT s ymptoms (V&D) are more acute than the general manifestations Pyrexia much lower and of shorter duration Malaria History of previous attacks More rapid onset Shivering and sweating High early pyrexia Relative infrequent abdominal symptoms and signs Positive blood smear Influenza More rapid onset High temperature, Severe sore throat and cough Absence of a palpable spleen and rose spots.

39. Bacillary dysentery Acute onset Severe bloody diarrhea The signs and symptoms in dysentery are usually abdominal Typhus and other rickettsial infections Acute onset High temperature at an early stage. Rigors are common Prostration is rapid. Rash is brownish red in colour , and much more profuse and does not fade on pressure. Leukocytosis Weil-Felix test becomes significantly positive at about the tenth day Tuberculosis (Abdominal/Pulmonary) The pyrexia and vague symptoms and signs may be very similar. A chest X-ray, or laboratory confirmation of typhoid, may be the only sure method of diagnosis. Brucellosis Onset tends to be more insidious. Painful joint is frequently present.

40. Treatment M ajority of children with typhoid fever can be managed at home with oral antibiotics and close medical follow-up for complications or failure of response to therapy. Patients with persistent vomiting , severe diarrhea, and abdominal distention may require hospitalization and parenteral antibiotic therapy . General Measure Adequate rest Adequate hydration correct fluid and electrolyte imbalance. Antipyretic therapy (Paracetamol 10-15 mg/ kgevery 4-6 hr PO) should be provided as required. Soft , easily digestible diet should be continued unless the patient has abdominal distention or ileus .

41. Antimicrobials Traditional therapy with chloramphenicol or amoxicillin is associated with relapse rates of 5-15 % and 4-8%, respectively U se of the quinolones and third generation cephalosporins is associated with higher cure rates. The antibiotic treatment of typhoid fever is also influenced by the prevalence of antimicrobial resistance. Emergence of multidrug-resistant strains of S. Typhi (i.e., isolates fully resistant to amoxicillin, trimethoprim-sulfamethoxazole , and chloramphenicol ) has necessitated treatment with fluoroquinolones with cephalosporins as an alternative. The emergence of resistance to quinolones places tremendous pressure on public health systems because alternative therapeutic options are limited. Azithromycin may be an alternative antibiotic for children with uncomplicated typhoid fever.

42. Guidelines for management of typhoid fever. WHO. July 2011

43. Dexamethasone (3 mg/kg for the initial dose, followed by 1 mg/kg every 6 hr for 48 hr ) is recommended for severely ill patients with shock, obtundation , stupor, or coma;

44. Fluoroquinolones : A dilemma!!! The fluoroquinolone drugs are generally very well tolerated. However, in some countries the use of fluoroquinolones is relatively contraindicated in children because of concerns that they may cause articular damage . There is now extensive experience in the use of these drugs in large numbers of children with long term follow-up. Their considerable benefits, particularly in areas where there are no affordable oral alternatives, outweigh the putative risk. The only known articular side effect is Achilles tendon rupture in patients who are also taking corticosteroids, and this has been reported only rarely . A Cochrane systematic review of the treatment of typhoid fever also indicates that there is little evidence to support the carte blanche administration of fluoroquinolones in all cases of typhoid fever

45. Why Fluoroquinolones??? High drug levels are achieved within the GI lumen after oral administration  no need of isolation The MIC for most salmonella is extremely low (<0.1mcg/ml) Bactericidal against Salmonella  low relapse Good Intracellular penetration  rapid onset and high cure rate Ciprofloxacin is concentrated in the biliary tract, a known site of persistent infection during chronic carriage of salmonella  prevention of carrier Oral form and IV form are available  cheap

46. Treatment of Carriers Drugs Duration Cure Rate Amoxicillin or Ampicillin (100 mg/kg/d) PLUS probenecid (1 g orally or 23 mg/kg) OR TMP-SMZ (160- 800 mg twice daily) 6 weeks 60% Ciprofloxacin (750mg twice daily) OR Norfloxacin (400mg twice daily) 28 days 80% Cholecytectomy may be required in chronic cases not treated by the above regimens and carriers with cholelithiasis Guidelines for management of typhoid fever. WHO. July 2011

47. Prevention

48. Best prevention Scrub them off your hands

49. Simple hand hygiene and washing can reduce several cases of Typhoid

50. Vaccination Typhoid vaccination was part of India’s national immunization program till 1985 Types of Typhoid Vaccines Whole cell inactivated typhoid/ paratyphoid (TAB ) Vaccine Vi-capsular polysaccharide (Vi-PS) vaccine live oral vaccine

51. Whole cell inactivated typhoid/ paratyphoid (TAB) Vaccine Type of Vaccine : Heat-inactivated phenol- preserved whole-cell Protective Efficacy: 51-88 % Age of vaccination: >6 mths of age Vaccination Schedule: 2 doses s.c 4 weeks apart Revaccination: 2 yrs Discontinued due to side effects like fever, malaise, local pain

52. Vi-capsular polysaccharide (Vi-PS) vaccine Type of Vaccine: Highly purified antigenic fraction of Vi antigen of S . typhi Protective Efficacy: 55-72 % Age of vaccination: >2 yrs of age Vaccination Schedule: single dose (25mcg of antigen) s.c. or i.m . Revaccination: 3yrs The vaccine is stable for 6 mths at 37ºC and for 2 yrs at 22ºC. It is not immunogenic in below 2 years of age and has no immune memory Protection begins seven days after injection and maximum reached at 28 days after injection

53. Live oral vaccine Type of Vaccine: live attenuated vaccine of Ty21a strain Protective Efficacy: 50-60 % Age of vaccination: > 6 yrs. Vaccination Schedule: 3 doses of enteric coated capsule(2-6 million bacteria) given on alternated days Revaccination:3yrs Antibiotics should not be given 3 days before and 7 days after vaccination Protection starts from 10-14 days after 3rd dose. Also provides Herd Immunity Contraindicated in immunodeficiency

54. Newer Vaccines Vi-capsular polysaccharide conjugated with Pseudomonas aeruginosa exotoxin A (Vi- rEPA ) Vi-PS Conjugate Vaccine Conjugated with Tetanus Toxoid ( Pedatyph ®) by Bio-Med Pvt. Ltd . Vi-polysaccharide conjugate vaccine conjugated with Tetanus Toxoid from Bharat Biotech ( Typbar -TCV®) S. paratyphi A vaccine composed of the surface O-specific polysaccharide conjugated with tetanus toxoid

55. References Ananthnarayan and Panikarys textbook of microbiology 7th edition Atul Kothari, Amit Pruthi , Tulsi D. Chugh . The Burden of Enteric Fever. J Infect Developing Countries 2008; 2(4): 253-259. Background document: The diagnosis, treatment and prevention of typhoid fever. World Health Organization. May-2003 Crump JA, Luby SP, Mintz ED (2004) The global burden of typhoid fever. Bull World Health Organ 82:346-353. Ghai Essential Pediatrics 8th Edition Guidelines for managemet of typhoid fever. WHO. July 2011 Huang DB, DuPont HL: Problem pathogens: extra-intestinal complications of Salmonella enterica serotype Typhi infection, Lancet Infect Dis 5:341–348, 2005 K. D. Moudgil M.D., B. S. Narang M.D., Pathogenesis of typhoid fever. The Indian Journal of Pediatrics July 1985, Volume 52, Issue 4, pp 371-378

56. IAP guidebook on immunization 2013-2014 IAP Task Force Report: Management of Enteric Fever in Children. Indian Pediatrics. Vol 43 Oct 2006 Manuela Raffatellu , R. Paul Wilson et al. Clinical pathogenesis of typhoid fever. J Infect Developing Countries 2008; 2(4): 260-266. Nelson Text of Pediatrics 19th Edition Ochiai RL, Acosta CJ, Danovaro -Holliday MC et al. (2008) A study of typhoid fever in five Asian countries: disease burden and implications for control. Bull World Health Organ 86(4):260-68. PG textbook of Pediatrics Sinha A, Sazawal S, Kumar R et al. (1999) Typhoid fever in children aged less than 5 years. Lancet 354:734-737 Victor Vaughan: A Biography of the pioneering Bacteriologist, 1851-1929 By Richard Adler YK Joshi. SYMPOSIUM : TYPHOID FEVER. Journal Indian Academy of Clinical Medicine, Vol. 2, No. 1 and 2 , January-June 2001

57. Thank You…