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Indian Pediatr 2018;55:408-410 |
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Hand, Foot and Mouth
Disease in the Andaman Islands, India
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Surya Palani 1,
Muruganandam Nagarajan1,
Ashok Kumar Biswas2,
Rajesh Reesu1 and
Vijayachari Paluru1
From 1Regional Medical Research Centre
(ICMR) and 2Andaman and Nicobar Islands Institute of Medical
Sciences; Port Blair, A & N Islands, India.
Correspondence to: Dr Vijayachari Paluru, Director
and Scientist-G, Regional Medical Research Centre (ICMR), Post bag No.
13, Dollygunj, Port Blair 744 101, Andaman and Nicobar Islands, India.
[email protected]
Received: July 13, 2016;
Initial review: November 03, 2016;
Accepted: March 10, 2018.
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Objectives: To investigate an outbreak of Hand,
foot and mouth disease (HFMD) in Andaman Islands during 2013.
Methods: Epidemiological, clinical data and samples were collected
from HFMD patients who attended selected hospitals. Data were analyzed
and samples were processed for detection of Enterovirus and further
confirmed by sequencing. Serotype-specific molecular typing was also
done to identify the etiological agent. Results: Of the 246
suspected patients, most were affected in August 2013 (92/246, 37.4%).
Fever (71.2%) associated with typical HFMD rashes (100%) were the most
common presenting symptoms and rashes were mostly distributed on hands
(100%), legs (92%), mouth (77%), and buttocks (52.8%). All cases were
reported as mild and recovered completely without any complications.
Enterovirus was detected in 63 cases (50.4%). Conclusion: HFMD
was mild, mostly reported in children <60 months of age, and in boys.
Coxsackie virus A16 was found to be the only etiological agent for this
specific outbreak.
Keywords: Epidemiology, Coxsackievirus-A16, Rash.
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H and, foot and mouth disease (HFMD) is
characterized by rashes or vesicular lesions mainly on the hands, feet
and mouth. It usually affects children, and is most commonly caused by
Enterovirus-A (EV-A) species, including Coxsackievirus-A16 (CV-A16) and
Enterovirus-71 (EV-71) [1]. Usually, HFMD caused due to CV-A16 is less
severe disease as compared to that caused by EV-71 [2]. However, severe
complications, including deaths have been reported rarely [3].
In India, outbreaks of HFMD have been reported from
various places, including Kerala, Odisha, Himachal
Pradesh and Uttarakhand [4-7]. Furthermore, there has been no
published report on epidemiological and clinical features of HFMD in the
Andaman and Nicobar (A&N) Islands, a remote group of islands in the Bay
of Bengal. In 2013, cases of HFMD were reported from various hospitals
in Port Blair. The present study aimed to explore the epidemiology,
clinical characteristics and causative agents of HFMD in these patients.
Methods
It was a hospital-based, observational study on
patients who were clinically diagnosed with HFMD at pediatric outpatient
department in three selected hospitals (GB Pant Hospital, INHS
Dhanvantri Hospital, and Chirayu Child Care Hospital) of Port Blair, the
A&N Islands. The study was approved by the Institutional Ethical
Committee, Regional Medical Research Centre (RMRC), Port Blair and the
Directorate of Health Services (DHS) of the A&N Islands, India. Children
presenting to these hospitals between August, 2013 and January, 2014
were included in the study. Additionally, a retrospective investigation
was also done for the period from 29th May, 2013 to 30th July, 2013 to
investigate and understand the epidemiology of the outbreak. The
patients and their parents/guardians were interviewed using the standard
virology case proforma available at RMRC that elicited epidemiological
and clinical information about each case. With their consent, at least
one of the possible samples viz. the external lesions swab,
throat swab, nasal swab and stool were collected from patients for
laboratory investigations. Patients were followed up till complete
recovery of illness. The patient was considered as positive for
laboratory tests if any of the specimens showed positivity.
Reverse-transcription nested PCR was performed to
screen for the presence of enterovirus targeting 5non-coding region
(5-NCR) [8,9]. Positive specimens were randomly selected for cDNA
sequencing. Molecular evolutionary genetic analysis was done using MEGA
6 software [10].
Phylogenetic tree was constructed using the neighbor-joining method with
bootstrap testing of 1000 replicates to estimate the stability of the
phylogenetic tree. The evolutionary distances were computed using the
Kimura 2-parameter method (K2P) as a method of nucleotide substitution.
The closely related genetic distance of the study isolates was inferred
by comparison with reference sequences, based on pair-wise genetic
distance. Furthermore, all the positive enterovirus specimens were
subjected for molecular typing specific to enterovirus serotypes viz.
CV-A16, EV-71 and CV-A6 targeting partial VP1 gene [11-13].
Results
Out of 246 clinically diagnosed HFMD cases in the
hospitals, 125 consented to participate in the study. Maximum (99.2%)
cases were reported from South Andaman district. The peak of the
outbreak was reached in the period from July to September, 2013
(203/246, 82.5%) with its highest peak in the month of August 2013 (n=92).
All 125 patients had characteristic rashes, including
maculopapular rash (72%), papular rash (38, 30.4%), petechial rash
(9,7.2%), erythematous rash (23, 18.4%), vesicular and pustular rash
(40, 32%), or oral ulcer (97, 77.6%). Rashes were distributed most
commonly on hands (125, 100%; predominantly on palms, dorsa of hand and
elbows), followed by legs (115, 92%;), mouth (97, 77.6%), buttocks (66,
52.8%), trunk (25, 20%), and face and neck (16, 12.8%). Most oral
lesions were observed in the palate (60, 61.9%), followed by buccal
mucosa (48, 49.5%), lips (42, 43.3%), tongue (33, 34%) and gingiva (25,
25.8%).
Other clinical features recorded were fever (89,
71.2%), chills and rigor (4, 3.2%), cough (43, 34.4%), cold (20, 16%),
coryza (16, 12.8%), sore throat (25, 20%), headache (4, 3.2%), abdominal
pain (9, 7.2%), vomiting (6, 4.8%), diarrhea (4, 3.2%), malaise (87,
69.6%), anorexia (88, 70.4%), and pruritus (9, 7.2%). All cases were
reported as mild; no severe complications/death were reported during the
study period. The rashes completely resolved within a period of 2 to 3
weeks of onset in all patients.
Sixty-three (50.4%) children were detected to be
positive for enterovirus infection. All enterovirus positive specimens
subjected for molecular typing confirmed that CV-A16 was responsible for
the specific outbreak in these islands during the study period.
Phylogenetic analysis (Web Fig. 1) showed that the study
isolates of Andaman were closely grouped with reference sequences of
mainland India (KT275250 and KT275251, K2P=0.008%), followed by Malaysia
(JQ746672 and JQ746678, K2P=0.018%).
Discussion
In this report, we documented an outbreak of HFMD
with its epidemiological and clinical features in Andaman and Nicobar
islands. All cases were mild, and Coxsackievirus-A16 was the causative
agent.
The study represents the patients reported to the
referral hospitals at South Andaman district only. The actual number of
cases during the outbreak is likely to be much higher as many patients
with mild disease may not have reported to the hospitals.
Like many other studies where HFMD outbreaks were
seen mostly in summer and fall [1], the peak of the outbreak in Andaman
Islands was also seen in the month of August with the similar seasonal
pattern. In the present report, with respect to the involvement of oral
mucosa, the number of lesions were more on the palate region unlike an
earlier report [6] from Shimla, India, where buccal mucosa was the most
common site (82.9%) followed by palate. Most of the signs and symptoms
in our series were almost similar to most other reported studies from
India [4,6]. However, a report from Southern India documented HFMD with
severe complications such as aseptic meningitis and acute encephalitis
syndrome in 12.3% of the total cases [14]. The causative agent CV-A16 of
the present outbreak was also commonly reported from other parts of the
country [15]. The probable reason of emergence of this disease in
Andaman islands could be the influx of tourists from mainland India to
these Islands.
Being one of the new illnesses, HFMD is also a threat
to public health of Andaman population, especially to the children.
Surveillance and public health awareness would help to keep the
infection localized to prevent future outbreaks.
Acknowledgements: The pediatricians and
dermatologists at GB Pant Hospital, INHS Dhanvantri, and Chirayu
Childcare Centre, Port Blair for their help in patient work-up. Anwesh
Maile for help in sequencing work.
Contributors: VP: study conception and
design; SP: study design, data analysis and drafted the first version of
manuscript; MN: interpretation of data; AKB: critically revised the
manuscript for important intellectual content. RR: helped in analysis of
the data and sample collection. The final manuscript was edited and
approved by all authors.
Funding: Indian Council of Medical Research,
Competing interests: None stated.
What This Study Adds?
Hand-Foot-Mouth Disease outbreak
due to Coxsackie virus A-16 with mild clinical course occurred
in Andaman and Nicobar Islands in 2013.
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References
1. Ang LW, Koh BK, Chan KP, Chua LT, James L, Goh KT.
Epidemiology and control of hand, foot and mouth disease in Singapore,
2001-2007. Ann Acad Med Singapore. 2009;38:106-12.
2. Chang LY, Lin TY, Huang YC, Tsao KC, Shih SR, Kuo
ML, et al. Comparison of Enterovirus 71 and Coxsackie-virus A16
clinical illnesses during the Taiwan enterovirus epidemic, 1998. Pediatr
Infect Dis J. 1999;18:1092-6.
3. Yang Z-Y, Chan X-Q, Sun D, Wei D. Mortality in
children with severe hand, foot and mouth disease in Guangxi, China.
Indian Pediatr. 2018;55:137-9.
4. Sasidharan CK, Sugathan P, Agarwal R, Khare S, Lal
S, Paniker CKJ. Hand-foot-and-mouth disease in Calicut. Indian J Pediatr.
2005;72:17-21.
5. Kar BR, Dwibedi B, Kar SK. An outbreak of hand,
foot and mouth disease in Bhubaneswar, Odisha. Indian Pediatr.
2013;50:139-42.
6. Kashyap S, Verma GK. Hand-foot-mouth disease:
outbreak in Shimla. Indian Pediatr. 2014;51:155.
7. Nanda C, Singh R, Rana SK. An outbreak of
hand-foot-mouth disease: A report from the hills of Northern India. Natl
Med J India. 2015;28:126-8.
8. Zoll GJ, Melchers WJ, Kopecka H, Jambroes G, van
der Poel HJ, Galama JM. General primer-mediated polymerase chain
reaction for detection of enteroviruses: Application for diagnostic
routine and persistent infections. J Clin Microbiol. 1992;30:160-5.
9. Puig M, Jofre J, Lucena F, Allard A, Wadell G,
Girones R. Detection of adenoviruses and enteroviruses in polluted
waters by nested PCR amplification. Appl Environ Microbiol.
1994;60:2963-70.
10. Tamura K, Stecher G, Peterson D, Filipski A,
Kumar S. MEGA6: Molecular evolutionary genetics analysis version 6.0.
Mol Biol Evol. 2013;30:2725-9.
11. Oberste MS, Maher K. Kilpatrick. DR, Flemister
MR, Brown BA, Pallansch MA. Typing of human enteroviruses by partial
sequencing of VP1. J Clin Microbiol. 1999;37:1288-93.
12. Yan JJ, Su IJ, Chen PF, Liu CC, Yu CK, Wang JR.
Complete genome analysis of enterovirus 71 isolated from an outbreak in
Taiwan and rapid identification of enterovirus 71 and coxsackievirus A16
by RT-PCR. J Med Virol. 2001;65:331-9.
13. Osterback R, Vuorinen T, Linna M, Susi P, Hyypia
T, Waris M. Coxsackievirus A6 and hand, foot, and mouth disease,
Finland. Emerg Infect Dis. 2009;15:1485-8.
14. Kumar VS, Budur SV, Odappa GH, Bankolli SY, Rao
AP. Clinical profile of hand, foot, and mouth disease and its associated
complications among children in Shimoga City, southern Karnataka: A
hospital-based study. Indian J Public Health. 2015;59:141-4.
15. Gopalkrishna V, Patil PR, Patil GP, Chitambar SD.
Circulation of multiple enterovirus serotypes causing hand, foot and
mouth disease. J Med Microbiol. 2012;61:420-5.
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