Published in IJCP April 2019
Clinical Study
Seroprevalence of Scrub Typhus and Clinical Profile of Children with Scrub Typhus Presenting to a Tertiary Care Hospital in a Rural Setting
April 10, 2019 | Judy Veronica J, Rajakumar PG, Jaishree V, Vikram R
     


Abstract

Introduction: Rickettsial infections were commonly recognized as an important cause of fever and central nervous system infections throughout Southeast Asia. Only in the recent years, it has been recognized to be an important cause of morbidity and mortality. Objective: To know the seroprevalence and clinical profile of children with scrub typhus presenting to a tertiary care hospital. Methodology: It was a cross-sectional study conducted in a tertiary health care center over a period of 1 year. Children presenting with fever for 5 days or more who were diagnosed negative for other causes of fever, like malaria and enteric fever, were considered as study population. A positive immunoglobulin M (IgM) ELISA (enzyme-linked immunosorbent assay) for scrub typhus was considered as primary outcome variable. Age, gender parameters were primary explanatory variables. Institutional ethical clearance was obtained. IBM SPSS version 22 was used for statistical analysis. Results: A total of 340 subjects were included in the final analysis. Among the study population, 241 (70.88%) children were aged >48 months. Male participants were 187 (55%) and remaining 153 (45%) were females. Out of 340 subjects, 48 (14.12%) participants were positive for scrub typhus. The common clinical features seen were fever, abdominal pain, cough, vomiting and hepatosplenomegaly in the decreasing order of frequency. Conclusion: The seroprevalence of scrub typhus rickettsial infection was 14.12%, which was quite high. Fever and abdominal pain were the prominent clinical features observed. Knowledge about scrub typhus fever may help in its early diagnosis and treatment and prevention of adverse outcome.

Keywords: Scrub typhus, prevalence, IgM ELISA

The infection caused due to Rickettsia normally presents as fever and is considered as one of the most significant central nervous system infections throughout Southeast Asia. Rickettsial infections are zoonotic infections. The transmission of rickettsial diseases is mainly through bites of arthropods like fleas, mites, etc. Rickettsia has three main serological groups of agents; scrub typhus is one of them. They are caused due to the serogroup Orientia tsutsugamushi and now there is newly discovered Orientia chuto, which is also known to cause scrub typhus fever. Scrub typhus is infectious in nature and trombiculid mites or chigger mites are mostly known for its transmission. The prevalence of scrub typhus infections is seen in areas of dense scrub vegetation. Hence, the name “scrub typhus” came into existence. Scrub typhus is endemic and is mainly found in the geographical region known as “tsutsugamushi triangle”. The region majorly lies in Asia, Australia, islands in the Indian and Pacific Oceans. The triangle runs from northern part of Japan via Russia in the north, to Pakistan and Afghanistan in the west, and via the territories around India into northern Australia in the south. However, currently, the scrub typhus is widespread and is occurring in locations that were not previously thought to be endemic.

The typical characteristic feature that differentiates scrub typhus fever from other infections is the necrotic black lesion called “eschar”, which is seen at the site of the mite bites. This helps in diagnosis of scrub typhus. The other signs and symptoms that are observed in scrub typhus cases include fever, chills, myalgia, headache, vomiting, diarrhea and rash. The complications may lead to acute renal failure, hepatitis, acute respiratory distress syndrome, meningitis, circulatory collapse and multiple organ dysfunctions.

Scrub typhus represents a major cause of treatable febrile illness across Asia. The prevalence of scrub typhus has been reported worldwide but the true incidence of the disease is still unknown. The extent of the disease is mainly seen in East and Southeast Asia such as Japan, Taiwan, China, South Korea, Nepal, Indonesia and Australia. A study by Balaji et al showed that 40% fever cases were positive for scrub typhus in Tamil Nadu and in another study, S Kanagasabai et al noted that 15% of the study subjects were positive for scrub typhus. The data on the prevalence of scrub typhus is scarce.

Scrub typhus with considerable morbidity and mortality has now been well-documented in several states in India and neighboring countries. Most studies in India are retrospective in nature or based on adult population. Hence, this study was carried out to know the seroprevalence and clinical profile of children with scrub typhus presenting to a tertiary care hospital in a rural Indian setting.

Material and Methods

Study Site

This study was conducted at the Dept. of Pediatrics of a tertiary care teaching hospital in a rural setting.

Study Population

Children up to 18 years of age, presenting with fever for 5 days or more and diagnosed negative for other causes of fever, like malaria and enteric fever, were considered as study population.

Study Design

The current study was a prospective cross-sectional study.

Sample Size

Sample size was calculated by assuming the expected prevalence of scrub typhus among the suspected cases as 56.42%, as per the previous published literature. The other parameters considered for sample size calculation included 10% absolute precision and 95% confidence level.

Sampling Method

All the eligible subjects were recruited into the study consecutively by convenient sampling till the sample size was reached.

Study Duration

The data collection for the study was done for 1-year period between July 2017 and June 2018.

Inclusion Criteria

Children aged less than 18 years, presenting with fever for 5 days or more.

Exclusion Criteria

  • Adults aged above 18 years.
  • Confirmed cases of malaria, enteric fever, leptospirosis.

Data Collection Tools

All the relevant parameters were documented in a structured study proforma.

Methodology

Statistical Methods

Scrub typhus immunoglobulin M (IgM) status was considered as primary outcome variable. Age, gender parameters were considered as primary explanatory variables.

Descriptive analysis was carried out by mean and standard deviation for quantitative variables, frequency and proportion for categorical variables.

The association between age, gender and scrub typhus IgM status was assessed by cross tabulation and comparison of percentages. Chi-square test was used to test statistical significance.

P value of <0.05 was considered statistically significant. IBM SPSS version 22 was used for statistical
analysis.

Observations and Results

A total of 340 subjects were included in the final analysis. Among the study population, 11 (3.24%) children were aged up to 12 months, 21 (6.18%) children were aged 13-24 months, 67 (19.71%) children were aged 25-48 months and 241 (70.88%) children were aged >48 months. Out of 340 children, male participants were 187 (55%) and remaining 153 (45%) were females.

Among the study population, 48 (14.12%) participants had positive results (Table 1).

Table 1. Seropositivity (IgM by ELISA) in Study Population (n = 340)

Result

Frequency

Percentage (%)

Positive

48

14.12

Negative

292

85.88

Out of 11 participants aged up to 12 months, 1 (9.090%) participant had positive result; of 21 participants aged 13-24 months, 1 (4.761%) participant had positive result. Out of 67 participants aged 25-48 months, 7 (10.44%) participants had positive result and among 241 participants aged >48 months, 39 (16.18%) participants had positive result (Table 2 and Fig. 1). The difference in the proportion of results across different age groups was statistically not significant (p value 0.343).

The majority of participants had fever. The proportion of patients with abdominal pain and cough was 79.17% each, and for vomiting, hepatosplenomegaly (HSM), headache and myalgia was 47.92%, 39.58%, 31.25% and 31.25% (Table 3). Among the study population, 85 (25%) participants had fever up to 5 days and 255 (75%) participants had fever >5 days.

Table 2. Comparison of Scrub Typhus Positivity with Age of the Study Population (n = 340)

Age group (in months)

Result

Chi-square

P value

Positive

Negative

Up to 12 (n = 11)

1
(9.090%)

10
(90.90%)

3.337

0.343

13-24 (n = 21)

1
(4.761%)

20
(95.23%)

25-48 (n = 67)

7
(10.44%)

60
(89.55%)

>48 (n = 241)

39
(16.18%)

202
(83.81%)


Figure 1. Stacked bar chart of scrub typhus positivity with age of the  study population (n = 340).

Table 3. Descriptive Analysis of Clinical Features in Study Population

Clinical Features

Frequency

Percentage (%)

Fever

48

100

Abdominal pain

38

79.17

Cough

38

79.17

Vomiting

23

47.92

HSM

19

39.58

Headache

15

31.25

Myalgia

15

31.25

Hepatomegaly

12

25.00

Poor appetite

10

20.83

Nausea

10

20.83

Rashes

9

18.75

Lymphadenopathy

9

18.75

Cool peripheries

8

16.67

Breathing difficulties

8

16.67

CRT >3 SEC

6

12.50

Conjunctival congestion

5

10.4

Splenomegaly

4

8.33

Jaundice

4

8.33

Seizure - I episode GTCS lasted for about 5 minutes

4

8.33

Melena

4

8.33

Oliguria

4

8.33

Cardiovascular dysfunction (shock) 

4

8.33

Eschar

8

16.67

Crepts and crackles

2

4.17

Petechiae

2

4.17

Neck stiffness

2

4.17

High-colored urine

2

4.17

Hematemesis

2

4.17

Discussion

In the current study, a total of 340 subjects were included in the final analysis. The study population varied in different studies. A study done in 2017 included only 96 participants, while a study done in 2018 had 964 patients.

Age

In the current study, 11 (3.24%) children were aged up to 12 months, 21 (6.18%) children were aged 13-24 months, 67 (19.71%) children were aged 25-48 months, 241 (70.88%) children were aged >48 months. In one study, the age ranged from 1 day to 18 years with the maximum number of children aged between 1 and 5 years (49.7%). In a study conducted in 2016, 13 (37%) subjects were aged between 1 and 5 years, 21 (60%) were aged >5-10 years and 6% were >10 years old. Various other studies reported the mean age as 8.97 ± 65.17, 7.3 ± 3.9, 3.2 ± 2.5 and 5.6 years.

In the current study population, 48 (14.12%) participants had positive results and 292 (85.88%) were negative for scrub typhus. The seroprevalence in our study was found to be 14.12%. The seroprevalence varied from 0.63% to 9.2% in various Indian studies.

Clinical Features in Study Population

A study in 2017 found that all the patients had fever. Other findings were also in accordance with our study where 56% of the participants had myalgia and 50.5% children experienced vomiting. Pallor was present in 48% of children, abdominal pain in 26% of the participants, headache in 28% children, facial puffiness in 15% participants and seizures in 8.7% participants. Other common signs were hepatomegaly in 29%, splenomegaly in 28%, hypotension in 24%, edema in 21%, oliguria in 17%, maculopapular rash in 10%, meningeal signs in 10.4% and conjunctivitis in 3% of the participants. Thrombocytopenia was seen in 67% participants, anemia in 51%, pleural effusion in 23%, shock in 16%, hepatitis in 23%, acute kidney injury in 17%, meningoencephalitis in 10%, myocarditis in 7% and acute respiratory distress
syndrome in 7%.

A study done in 2009 found that the primary clinical symptoms included fever (100%), cough (50%), eschar (50%), rash (35.7%), poor appetite (42.9%), lymphadenopathy (42.9%), headache (39.3%) and hepatomegaly (35.7%). All these were in accordance with our study.

Eschar

In the current study, eschar in axilla was seen in 14.4%. In another study, eschars were often on the axilla/groin in 24.9% participants, followed by 23.4% in the abdominal region and waist area and 18.3% in the head and neck region.

Fever (in Days)

Among the study population, 85 (25%) participants had fever up to 5 days and 255 (75%) participants had fever for >5 days. In a study, 18 (27%) patients had fever <7 days, 39 (59%) had fever for 7-14 days and 9 (14%) had fever for >14 days. A study done in 2017 reported the mean days of fever to be 8.856 ± 3.18.

Limitations

  • The present study was conducted only in pediatric population and was conducted at a single center. Hence, the study cannot be generalized to the rest of the population.
  • Purposive sampling technique was employed for the study which is not a true representation of the general population. This may lead to selection bias.
  • The study was hospital-based leading to Berksonian bias.

Recommendations

Given that there was high prevalence of scrub typhus rickettsiosis in our study, the clinicians and general practitioners must be aware of the clinical profile related to scrub typhus fever. Rickettsial fever must be considered when the symptoms don’t fit into the profile of any other diseases causing fever (dengue, malaria, etc.). Timely recognition of complications may help prevent the adverse outcome.

It is recommended to conduct a large multicentric population-based study to know the true prevalence of scrub typhus.

Conclusion

The seroprevalence in our study was found to be 14.12% which was quite high when compared to previous studies.

Suggested Reading

  1. Trung NV, Hoi LT, Thuong NTH, Toan TK, Huong TTK, Hoa TM, et al. Seroprevalence of scrub typhus, typhus, and spotted fever among rural and urban populations of Northern Vietnam. Am J Trop Med Hyg. 2017;96(5):1084-7.
  2. Bonell A, Lubell Y, Newton PN, Crump JA, Paris DH. Estimating the burden of scrub typhus: A systematic review. PLoS Negl Trop Dis. 2017;11(9):e0005838.
  3. Jiang J, Richards AL. Scrub typhus: no longer restricted to the tsutsugamushi triangle. Trop Med Infect Dis. 2018;3(1). pii: E11.
  4. Ramyasree A, Kalawat U, Rani ND, Chaudhury A. Seroprevalence of Scrub typhus at a tertiary care hospital in Andhra Pradesh. Indian J Med Microbiol. 2015;33(1):68-72.
  5. Saleem M, Shivekar S, Gopal R. Clinico laboratory profile of scrub typhus at a rural tertiary hospital in South India. Int J Curr Res Rev. 2015;7(10):75-8.
  6. Xu G, Walker DH, Jupiter D, Melby PC, Arcari CM. A review of the global epidemiology of scrub typhus. PLoS Negl Trop Dis. 2017;11(11):e0006062.
  7. Balaji J, Punitha P, Babu BR, Kumaravel K. A study on clinical profile, complications and outcome of scrub typhus in South Indian children. Int J Contemp Pediatr. 2017;4(3):848-52.
  8. Kanagasabai S, Thatchinamoorthy G, Ganesan A, Pachiyappan G, Gouthami P, Valarmathi S, et al. Seroprevalence of Scrub typhus and coinfection with leptospirosis in Chennai, Tamil Nadu. Int J Infect Dis. 2016;45(Suppl 1):178.
  9. Kumar M, Krishnamurthy S, Delhikumar CG, Narayanan P, Biswal N, Srinivasan S. Scrub typhus in children at a tertiary hospital in southern India: clinical profile and complications. J Infect Public Health. 2012;5(1):82-8.
  10. Jeong YJ, Kim S, Wook YD, Lee JW, Kim KI, Lee SH. Scrub typhus: clinical, pathologic, and imaging findings. Radiographics. 2007;27(1):161-72.
  11. George T, Rajan SJ, Peter JV, Hansdak SG, Prakash JAJ, Iyyadurai R, et al. Risk factors for acquiring scrub typhus among the adults. J Glob Infect Dis. 2018;10(3):147-51.
  12. Seong SY, Choi MS, Kim IS. Orientia tsutsugamushi infection: overview and immune responses. Microbes Infect. 2001;3(1):11-21.
  13. Lim VK. Occupational infections. Malays J Pathol. 2009;31(1):1-9.
  14. Sharma PK, Ramakrishnan R, Hutin YJ, Barui AK, Manickam P, Kakkar M, et al. Scrub typhus in Darjeeling, India: opportunities for simple, practical prevention measures. Trans R Soc Trop Med Hyg. 2009;103(11):1153-8.
  15. Li T, Yang Z, Dong Z, Wang M. Meteorological factors and risk of scrub typhus in Guangzhou, southern China,
    2006-2012. BMC Infect Dis. 2014;14:139.
  16. Jeung YS, Kim CM, Yun NR, Kim SW, Han MA, Kim DM. Effect of latitude and seasonal variation on scrub typhus, South Korea, 2001-2013. Am J Trop Med Hyg. 2016;94(1):22-5.
  17. Devine J. A review of scrub typhus management in 2000-2001 and implications for soldiers. J Rural Remote Environ Health. 2003;2(1):14-20.
  18. Peter JV, Sudarsan TI, Prakash JA, Varghese GM. Severe scrub typhus infection: Clinical features, diagnostic challenges and management. World J Crit Care Med. 2015;4(3):244-50.
  19. Sharma R. Scrub typhus: prevention and control. JK Science. 2010;12(2):91.
  20. Rahi M, Gupte MD, Bhargava A, Varghese GM, Arora R. DHR-ICMR Guidelines for diagnosis & management of Rickettsial diseases in India. Indian J Med Res. 2015;141(4):417-22.
  21. Koh GC, Maude RJ, Paris DH, Newton PN, Blacksell SD. Diagnosis of scrub typhus. Am J Trop Med Hyg. 2010;82(3):368-70.
  22. Jamil M, Lyngrah KG, Lyngdoh M, Hussain M. Clinical manifestations and complications of scrub typhus: a hospital based study from North Eastern India. J Assoc Physicians India. 2014;62(12):19-23.
  23. Tsay RW, Chang FY. Serious complications in scrub typhus. J Microbiol Immunol Infect. 1998;31(4):240-4.
  24. De Silva N, Wijesundara S, Liyanapathirana V, Thevanesam V, Stenos J. Scrub typhus among pediatric patients in Dambadeniya: a base hospital in Sri Lanka. Am J Trop Med Hyg. 2012;87(2):342-4.
  25. Huang CT, Chi H, Lee HC, Chiu NC, Huang FY. Scrub typhus in children in a teaching hospital in eastern Taiwan, 2000-2005. Southeast Asian J Trop Med Public Health. 2009;40(4):789-94.
  26. Liu YX, Jia N, Suo JJ, Xing YB, Liu G, Xiao HJ, et al. Characteristics of pediatric scrub typhus in a new endemic region of northern China. Pediatr Infect Dis J. 2009;28(12):1111-4.
  27. Liu YX, Zhao ZT, Feng PT, Ma SB, Min JS, Qin DT, et al. Clinical manifestations and epidemic factors of autumn-winter type scrub typhus in children from northern new endemic area. Zhonghua Er Ke Za Zhi. 2008;46(2):128-31.
  28. Maina AN, Farris CM, Odhiambo A, Jiang J, Laktabai J, Armstrong J, et al. Q Fever, scrub typhus, and rickettsial diseases in children, Kenya, 2011-2012. Emerg Infect Dis. 2016;22(5):883-6.
  29. Zhao D, Zhang Y, Yin Z, Zhao J, Yang D, Zhou Q. Clinical predictors of multiple organ dysfunction syndromes in pediatric patients with scrub typhus. J Trop Pediatr. 2017;63(3):167-73.
  30. Mittal M, Thangaraj JWV, Rose W, Verghese VP, Kumar CPG, Mittal M, et al. Scrub typhus as a cause of acute encephalitis syndrome, Gorakhpur, Uttar Pradesh, India. Emerg Infect Dis. 2017;23(8):1414-6.
  31. Bithu R, Kanodia V, Maheshwari RK. Possibility of scrub typhus in fever of unknown origin (FUO) cases: an experience from Rajasthan. Indian J Med Microbiol. 2014;32(4):387-90.
  32. Peesapati N, Lakkapragada R, Sunitha S, Sivaram Clinical manifestations and complications of scrub typhus: A hospital-based study from North Andhra. Astrocyte. 2015;2(3):116-20.
  33. Singh SP, Singh R, Ahmad N. A study of complications of scrub typhus in a tertiary health care institute of Uttarakhand, India. Int J Res Med Sci. 2014;2(1):246-9.
  34. Choudhury J, Rath D, Sahu R. Scrub typhus in children at a tertiary care hospital in Odisha: A study on clinical, laboratory profile, complications and its outcome. Ann Int Med Den Res. 2016;2(4):213-6.
  35. Ganesh R, Suresh N, Pratyusha LL, Janakiraman L, Manickam M, Andal A. Clinical profile and outcome of children with scrub typhus from Chennai, South India. Eur J Pediatr.2018;177(6):887-90.
  36. Giri PP, Roy J, Saha A. scrub typhus - a major cause of pediatric intensive care admission and multiple organ dysfunction syndrome: a single-center experience from India. Indian J Crit Care Med. 2018;22(2):107-10.
  37. Kumar M, Krishnamurthy S, Delhikumar CG, Narayanan P, Biswal N, Srinivasan S. Scrub typhus in children at a tertiary hospital in southern India: clinical profile and complications. J Infect Public Health.2012;5(1):82-8.
  38. Masand R, Yadav R, Purohit A, Tomar BS. Scrub typhus in rural Rajasthan and a review of other Indian studies. Paediatr Int Child Health. 2016;36(2):148-53.
  39. Palanivel S, Nedunchelian K, Poovazhagi V, Raghunadan R, Ramachandran P. Clinical profile of scrub typhus in children. Indian J Pediatr. 2012;79(11):1459-62.
  40. Kumar S, Kumar M, Aggarwal B, Kumari R. Scrub typhus in children: clinical profile and complications at a tertiary care teaching hospital in Uttarakhand. Indian J Child Health. 2017;4(2):188-92.
  41. Borkakoty B, Jakharia A, Biswas D, Mahanta J. Co-infection of scrub typhus and leptospirosis in patients with pyrexia of unknown origin in Longding district of Arunachal Pradesh in 2013. Indian J Med Microbiol. 2016;34(1):88-91.
  42. Bhat NK, Pandita N, Saini M, Dhar M, Ahmed S, Shirazi N, et al. Scrub typhus: a clinico-laboratory differentiation of children with and without meningitis. J Trop Pediatr. 2016;62(3):194-9.
  43. Rathi NB, Rathi AN, Goodman MH, Aghai ZH. Rickettsial diseases in central India: proposed clinical scoring system for early detection of spotted fever. Indian Pediatr. 2011;48(11):867-72.
  44. Kalal BS, Puranik P, Nagaraj S, Rego S, Shet A. Clinical profile and serological epidemiology of scrub typhus and spotted fever among hospitalized children at a tertiary hospital in South India. Int J Infect Dis. 2016;45 Suppl 1:177-8.
  45. Ratageri VH, Madhu P, Sindhu M, Illalu S, Shepur T. Clinico-laboratory profile and outcome of rickettsia in children: Hubli (Karnataka) experience. Pediatr Infect Dis. 2014;6(1):3-6.
  46. Jakharia A, Borkakoty B, Biswas D, Yadav K, Mahanta J. Seroprevalence of scrub typhus infection in Arunachal Pradesh, India. Vector Borne Zoonotic Dis. 2016;16(10):659-63.
  47. Kumar Bhat N, Dhar M, Mittal G, Shirazi N, Rawat A, Prakash Kalra B, et al. Scrub typhus in children at a tertiary hospital in north India: clinical profile and complications. Iran J Pediatr. 2014;24(4):387-92.
  1. Dinesh Kumar N, Arun Babu T, Vijayadevagaran V, Ananthakrishnan S, Kittu D. Clinical Profile of scrub typhus meningoencephalitis among South Indian Children. J Trop Pediatr. 2018;64(6):472-8.