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STIs in children
and adolescents
had no controls, or used control groups that did not exclude girls
with a history of abuse or who were screened only for current
sexual activity.
Children and adolescents should be seen in the most appropriate site for optimal care. Adolescents are at high risk of pregnancy
and STIs, and may be less compliant with medication and partner
notification. Confidentiality and empathic staff are important in
attracting them to services.
Angela J Robinson
Epidemiology
The risk of contracting an STI depends on several factors
(Figure 2).
In infancy, infection may be related to prolonged colonization
after perinatal acquisition. Uncertainty over incubation periods of
infections prevents the setting of rigid upper age limits after which
abuse is most likely.
In older children with an STI, a history of vaginal/rectal
penetration or apposition of genitals can usually be obtained,
though disclosure may be delayed. In some studies, assessment
to determine whether abuse had occurred was deficient.1 In the
largest epidemiological study of the prevalence of sexually transmitted organisms, findings were reported in 1538 children aged
112 years who were evaluated for possible sexual abuse. Neisseria
gonorrhoeae was found in 41/1469 (2.8%), human papillomavirus
(HPV) causing condylomata acuminata in 28/1538 (1.8%) and
Chlamydia trachomatis in 17/1473 (1.2%).2 The overall prevalence
of definitely sexually transmitted organisms was less than 5%,
consistent with other studies.
In adolescents, consensual sexual activity is more likely to be
the transmission mode, though sexual abuse should be considered.
Data obtained through GUM clinics indicate that adolescents are
at highest risk of STIs. Between 1995 and 2003, rates of diagnoses
of gonorrhoea and chlamydial infection increased by 170% and
242% in women aged 1619 years. Re-infection rates are greatest
in adolescents.3
General considerations
There are important anatomical and physiological differences
between the genital organs of adults, adolescents and children.
Hormonal changes influence the microbiological flora of the genital
tract. The presence of some micro-organisms can be considered
normal or potentially pathogenic. Current understanding of the
normal vaginal flora in children is limited. Some studies have
compared children with vulvovaginitis with a control group without addressing the possibility of sexual abuse. Other investigators
Diagnosis
Symptoms such as dysuria, genital discharge, pruritus, soreness
and pain are nonspecific indicators of STI and have many other
causes. Some infections, particularly C. trachomatis and rectal
and/or pharyngeal gonorrhoea, can be asymptomatic.
Perinatal
Direct contact
Non-sexual/auto-inoculation
Fomites
?Trichomonas vaginalis
All STIs
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not been validated in prepubertal children. The latter investigation may be sufficently legally robust, but there have been few
test cases. Ideally, culture confirmation is needed, but culture is
seldom available except in specialist laboratories. NAATs may be
useful as screening tests for Chlamydia and N. gonorrhoeae, but
for evidence in court, confirmation by another NAAT or culture
for Chlamydia and by gonococcal culture is recommended.
The wet preparation for trichomoniasis and clue cells, and the
amine or whiff test are possible only when vaginal discharge is
present. A discharge sample can be taken with a swab and placed
in Amies medium for microscopy and culture.
A clotted blood sample can be taken for syphilis, hepatitis B/C
and HIV serology. Testing should be considered on an individual
basis, depending on the prevalence of these infections in the
population and other risk factors (see below).
Chain of evidence if the presence of infection is used as
evidence in court proceedings, it is essential to follow a chain of
evidence procedure, in which a form is signed as the samples are
handed from one individual to the next. Written protocols should
be agreed between microbiology, paediatric and GUM departments,
to ensure that the correct procedures are followed.
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Management antibiotic treatment is based on the local sensitivity of N. gonorrhoeae. Recently, gonorrhoea has become resistant
to fluoroquinolones, and third-generation cephalosporins are now
recommended in adults.
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abused was 42% (range 3.3100%). The risk of genital warts following abuse is difficult to assess, because of lack of long-term
follow-up data after diagnosis of sexual abuse.
The peak age of incidence is between birth and 4 years. Reports
of anogenital warts in girls are twice as common as those in
boys.
Clinical features and diagnosis condylomatous, papular
and flat warts are seen in children. They may be asymptomatic
or may cause soreness, irritation and bleeding. Anogenital warts
are usually found around the vaginal introitus, on the perineum
and around the anus in girls. In boys, they are most common on
the perianal and perigenital areas. Penile condylomata are rare.
Diagnosis is clinical and can be confirmed by biopsy. DNA
subtyping of HPV is of limited value, but should be considered
to indicate whether the wart is of genital or non-genital type.
However, genital HPV types can be transmitted vertically, and
non-genital wart types can be transmitted by abuse (e.g.fondling/
digital penetration). Examination of parents/carers and siblings
for evidence of infection may provide useful information and is
recommended, as is long-term follow-up in view of the risk of
subsequent anogenital neoplasia.
Management options include a period of observation; many
cases resolve spontaneously. Location, severity, age of the child
and the potential discomfort of the procedure should be considered when deciding treatment. Physician-applied or parentapplied podophyllotoxin, cryotherapy or surgical removal under
general anaesthesia can be used, but their adequacy is uncertain
because there are few large studies. Long-term follow-up is often
lacking.
Appropriate tests should be undertaken to exclude other
STIs.
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REFERENCES
1 Beck- Sague C M, Solomon F. Sexually transmitted diseases in abused
children and adolescent and adult victims of rape: review of selected
literature. Clin Infect Dis 1999; 28: (Suppl. 1): S7483.
2 Ingram D L, Everett D, Lyna P et al. Epidemiology of adult sexually
transmitted disease agents in children being evaluated for sexual
abuse. Pediatr Infect Dis 1992; 11: 94550.
3 Health Protection Agency. Focus on prevention. London: Health
Protection Agency, 2004.
4 Heger A, Ticson L, Velasquez O et al. Children referred for possible
sexual abuse: medical findings in 2384 children. Child Abuse Neglect
2002; 26: 64559.
FURTHER READING
British Medical Association. Consent, rights and choices in health care
for children and young people. London: BMA, 2000.
Department of Health. Working together. The Children Act 1989. A guide
to arrangements for interagency cooperation for the protection of
children from abuse. London: HMSO, 1990.
Hay P E. The diagnosis and management of vaginal discharge. In:
Barton S E, Hay P E, eds. Handbook of genitourinary medicine.
London: Arnold, 2000: 849.
Heger A, Jean Emans S, eds. Evaluation of the sexually abused child.
2nd ed. New York: Oxford University Press, 2000.
Joishy M, Ashtekar C S, Jain A et al. Do we need to treat vulvovaginitis in
pre-pubertal girls? BMJ 2005; 330: 1868.
Robinson A J. The clinical examination and how to obtain specimens.
In: Barton S E, Hay P E, eds. Handbook of genitourinary medicine.
London: Arnold, 2000: 1617.
Robinson A J, Ridgway G L. Sexually transmitted diseases in children:
non-viral including bacterial vaginosis, Gardnerella vaginalis,
mycoplasmas, Trichomonas vaginalis, Candida albicans, scabies and
pubic lice. Genitourin Med 1994; 70: 20814.
Royal College of Physicians. Physical signs in child sexual abuse. 2nd ed.
London: Royal College of Physicians, 1997.
Thomas A, Forster G, Robinson A et al. National guideline on the
management of suspected sexually transmitted infections in children
and young people. Sex Transm Infect 2002; 78: 32431. www.bashh.
org/guidelines
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