Sexually transmitted infections

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21 Sexually transmitted infections

Introduction

There are two main principles in the management of sexually transmitted infections. First, an infected patient implies that at least one other person is also infected. Thus, treating a patient in isolation will not control the spread of these diseases. Second, a patient may harbour more than one sexually transmitted infection (Box 21.1). Many infections are asymptomatic, acquired months or even years previously. Patients are often uncomfortable or embarrassed to give their sexual history or a history of genitourinary symptoms as stigma and shame are often attached to sexually transmitted infections. Remember that babies, monogamous partners and victims of rape and sexual abuse can also be infected.

The interview and examination must be carried out in private, in strict confidence and avoiding any disapproving, judgemental or moralistic attitude. As with other clinical problems, diagnosis is achieved by history (Box 21.2), examination and relevant laboratory tests. Following diagnosis, effective treatment and partner notification/contact tracing should be instituted promptly. In children under 16 years of age, ensure they are able to comprehend (follow the Fraser’s guidelines in the UK) and it is essential to exclude any child protection issues and sexual abuse.

History

Presenting symptoms

Sexual history

Enquiry into the less embarrassing aspects of the medical history fosters the patient’s confidence, so start with this before moving on to more intimate matters, such as (in the case of women) contraception and the menstrual history. Details of the sexual history should be obtained by simple questions. Ascertain the date of exposure: ‘When did you last have intercourse/sex?’ and particulars of sexual contacts over recent months. Heterosexual, homosexual or bisexual contact should be ascertained: ‘Do you have intercourse/sex with men, women or both?’ If married: ‘When did you last have intercourse/sex with your wife/husband?’ followed by ‘When did you last have intercourse/sex with someone else?’ and whether with regular partners, casual contacts or commercial sex workers (Did you pay for sex?). Are sexual partners traceable, for example place of intercourse: ‘which town?’ and ‘whether abroad?’ If there are several contacts, it is useful to identify them by first names.

The incubation period of infection may be assessed from the date of exposure to the onset of symptoms, and hence the probable cause. Tropical sexually transmitted infections should also be considered in patients presenting with genital problems acquired in the tropics. A history of intercourse with homosexual or bisexual men, injecting drug users or persons in or from an area of high HIV endemicity suggest AIDS as the cause of multisystemic symptoms and signs.

The type of sexual practice will dictate the sites from which to take tests (see below). It is also helpful to understand some of the common or unfamiliar terms that may be used in relation to sexual practices. ‘Straight sex’ indicates heterosexual (penovaginal) intercourse. Ask whether the person also practises insertive or receptive oropenile intercourse: ‘Do you receive or give ‘oral sex’?’ Certain practices in homosexual or bisexual men (‘gay sex’) may predispose to particular infections; for example, if there is oroanal contact, the possibility of intestinal pathogens should be considered. Hepatitis B and HIV infections are more common in those practising receptive penoanal intercourse. Ask whether the patient practises insertive (‘active’, ‘give anal sex’) or receptive (‘passive’, ‘receive anal sex’) penoanal intercourse: ‘When did you last have anal sex?’, ‘Do you give or receive anal sex?’ or simply ‘Are you ‘active’, ‘passive’ or both?’ Some patients practise oroanal intercourse (‘rimming’), insertive or receptive brachioanal intercourse (‘fisting’) and, rarely, urinating onto each other (‘watersports’) or using faeces during intercourse (’scat’). ‘Bare backing’ is unprotected anal intercourse; ‘cottaging’ is sexual intercourse in public places.

Heterosexual couples may also practise penoanal intercourse. This should be enquired for if rectal infection is found in women, although this commonly occurs in association with infection at other genital sites without having anal sex. Sex ‘toys’ or ‘dildoes’ (artificial penises) are objects inserted into the rectum or vagina. ‘Fisting’ and ‘toys’ may cause injury presenting as an acute abdomen. ‘Bondage’, in which the person is tied up during sex, may be associated with masochism (sexual gratification through the infliction of pain on another). This should be considered if superficial injuries are present without an obvious cause.

Enquire about the use of condoms whether or not the patient is using other methods of contraception. Condom use should be advised if the person is at risk of acquiring or transmitting sexually transmitted infections, or if the efficacy of an oral contraceptive is affected by the concomitant use of other drugs. Many infections that may initially be acquired through non-sexual means, for example hepatitis B and HIV infection among injecting drug users and haemophiliacs, may be secondarily transmitted through sexual intercourse. Advice on non-penetrative ‘safer sex’ practices, such as body rubbing, dry kissing and masturbating each other, can be given to infected individuals who do not wish to have penetrative intercourse.

Sexual dysfunction, including erectile problems, premature and retarded ejaculation, often presents to a sexually transmitted disease clinic. Impotence is likely to be psychogenic if it is sudden in onset, related to life events, situational or intermittent, or if nocturnal or early morning erections are unaffected, and organic causes often have a psychogenic component. Curvature of the penis on erection may result from Peyronie’s penile fibrosis.

Genital examination

The patient should be examined in a well-lit room and gloves should always be worn. Chaperoning should be offered; female patients must be chaperoned when examined by male clinicians.

Male genitalia

The penis

Note the appearance and size of the penis, the presence or absence of the prepuce and the position of the external urethral orifice. Examine the penile shaft for warts, molluscum, ulcers, burrows and excoriated papules of scabies and rashes. In Peyronie’s disease, there may be induration or a fibrotic lump inside the penile shaft. In the uncircumcised, establish that the prepuce can be readily retracted by gently withdrawing it over the glans penis. This allows inspection of the undersurface of the prepuce, the glans, the coronal sulcus and the external urethral orifice (meatus) for warts (Fig. 21.1), inflammation, ulcers and other rashes. Always carefully draw the prepuce forwards after examination; otherwise paraphimosis – painful oedema of the foreskin due to constriction by a retracted prepuce – may ensue.

Phimosis is narrowing of the preputial orifice, thereby preventing retraction of the foreskin; it may be due to lichen sclerosus. This predisposes to recurrent episodes of infection of the glans (balanitis), the prepuce (posthitis) or both (balanoposthitis). Circinate balanitis in Reiter’s disease appears as erythematous eroded lesions which coalesce with a slightly raised and polycyclic edge. Multiple small yellow or white submucous deposits (Fordyce’s spots) may be seen on the inner prepuce. These are ectopic sebaceous glands and do not require treatment. Smegma, which is greyish–white cheesy material arising from Tyson’s glands, may accumulate under the prepuce if unwashed.

Hypospadias is a congenital abnormality in which the external urethral orifice is not at the tip of the glans penis but opens at its ventral surface in the midline, anywhere from the glans to the shaft, or even in the perineum. Epispadias, a similar opening situated on the dorsal surface of the penis, is rare.

Tiny regular papules arranged in rows around the coronal sulcus are coronal papillae and may be mistaken for warts. The coronal sulcus is the commonest site for a chancre. Inspect the meatus for inflammation, urethral discharge, narrowing (stricture) and warts. Retract the lips of the meatus to look for meatal chancre and intrameatal warts. Tyson’s gland is on the fraenum of the penis and is not normally palpable, whereas the median raphe leads from the fraenum to the inferior aspect of the penile shaft; both can be infected by gonococcal or chlamydial infection, leading to tysonitis and median raphe abscess, respectively.

Look at the scrotal skin for any redness, swelling or ulcer. Lift the scrotum to inspect its posterior surface. Tiny dark-red papules of angiokeratoma, or round, firm, whitish nodules of sebaceous cysts can sometimes be seen. Scabies causes erythematous nodular lesions on the scrotum and glans penis. If intrascrotal swelling is present, observe whether it appears to extend into the groin and note whether both testes are in the scrotum. Ulceration can result from Behçet’s disease, fungation of an underlying tumour of the testis, or from a gumma.

The testes

Place both hands below the scrotum, the right hand being inferior, and palpate both testes. Arrange the hands and fingers as shown in Figure 21.2: this ‘fixes’ the testis so that it cannot slip away from the examining fingers. The posterior aspect of the testis is supported by the middle, ring and little fingers of each hand, leaving the index finger and thumb free to palpate. Gently palpate the anterior surface of the body of the testis; feel the lateral border with the index finger and the medial border with the pulp of each thumb. Note the size and consistency of the testis and any nodules or other irregularities. Now very gently approximate the fingers and thumb of the left hand (the effect of this is to move the testis inferiorly, which is easily and painlessly done because of its great mobility inside the tunica vaginalis). In this way, the upper pole of the testis can be readily felt between the approximated index finger and thumb of the left hand. Next move the testis upwards by reversing the movements of the hands and gently approximating the index finger and thumb of the right hand, so enabling the lower pole to be palpated. The normal testes are equal in size, varying between 3.5 and 4 cm in length.

The spermatic cord

Finally palpate the spermatic cord with the right hand. Then exert gentle downward traction on the testis, place the fingers behind the neck of the scrotum and, with the thumb placed anteriorly, press forward with fingers of the right hand. The spermatic cord will be felt between the fingers and thumb; it is about 1 cm in width. The only structure that can be positively identified within it is the vas deferens, which feels like a thick piece of string.

Repeat the examination on the other side. Remember that the patient should also be examined standing up to look for varicocele – dilated tortuous veins like a bag of worms in the scrotum. Hydrocele of the tunica vaginalis or cysts of the epididymis are common causes of a painless scrotal swelling. Hydrocele can be demonstrated by transillumination, using a bright light source held in contact with the enlarged testicle, preferably in a darkened room. A painless, unilateral, hard, enlarged testis must be considered malignant. Other painless enlargements include testicular gumma and tuberculous involvement. Acute epididymo-orchitis, torsion of the testis, strangulated inguinal hernia and some cases of testicular neoplasm cause a painful swelling. In torsion, the epididymis cannot be differentiated from the swollen testis, which lies at a higher level than the normal testis. In old age, the testes may become atrophic. In younger men, testicular atrophy often indicates chronic liver disease, usually alcoholic in aetiology, or it may be associated with previous torsion or varicocele. In swellings of uncertain origin, ultrasound is useful.

Female genitalia

It is best to examine women in the lithotomy position. Examine the perineum, vulva and labia majora and minora for discharge, redness, swelling, excoriation, ulcers, warts and other lesions. In rape and sexual abuse cases, look for evidence of trauma. In such cases, forensic and genital examination by specially trained personnel may be required. Redness and swelling of the vulva with excoriations may be seen in thrush and trichomoniasis. Separate the labia and palpate the Bartholin’s glands: normally they are not felt. Bartholin’s abscess may result from gonococcal or chlamydial infection, and purulent discharge may be observed from Bartholin’s duct, which is between the upper two-thirds and lower one-third of the labia. Wipe away any contaminating vaginal discharge from the urethral meatus and insert a bivalve Cusco speculum moistened with water or lubricating jelly. Lubricating jelly should not be used if a cervical cytological smear is to be performed. Note any inflammation of the vaginal wall (vaginitis) and the colour, consistency and odour of any discharge. A curd-like or cheesy white discharge suggests thrush, a frothy greenish-yellow discharge trichomoniasis and an off-white homogeneous discharge bacterial vaginosis. The last two conditions also have a fishy odour. Take tests (see below) from the posterior fornix of the vagina.

Wipe the cervix with a swab and examine it for discharge from the external cervical os, for ectopy or ectropion (ectopic columnar epithelium) and for cervicitis, warts and ulcers. Nabothian follicles may present as yellowish cysts, which may have prominent vessels on their surface, and are normal. Mucopurulent cervicitis may be caused by gonococcal or chlamydial infections (Fig. 21.3). Warts on the cervix appear as either flat or papilliferous lesions. Take tests, including a smear for cervical cytology, if indicated, to detect dysplasia and cancer of the cervix. This is particularly important because of the association of cervical cancer with oncogenic human papilloma virus infections. Then remove the speculum. Next examine the urethral orifice for discharge, inflammation and warts, and take endourethral tests (see below). Examine the anal region for lesions, as in homosexual men. If indicated, insert a lubricated proctoscope and examine the rectal mucosa for discharge or inflammation, and take tests.

HIV infections

The worldwide spread of HIV infection has resulted in a dramatic lowering of life expectancy in some countries, especially in Africa. HIV infection is categorized into A, B and C (Box 21.3), based broadly on the clinical evolution of the immunodeficiency state that leads to the development of the acquired immune deficiency syndrome (AIDS), on average some 8-15 years after infection if untreated.

Box 21.3 Centre for Disease Control (CDC) HIV clinical categories

Assessment of the patient with HIV infection should assess the extent of the disease and its complications. Multisystem involvement is common, and in each system there may be multiple causes. Examination of the mouth and the skin may provide clues that a patient is immunosuppressed. Common chest infections include tuberculosis, Pneumocystis and other bacterial pneumonias. Common cerebral lesions include toxoplasmosis, tuberculoma, other bacterial or fungal abscesses and lymphoma. Diarrhoea may be caused by HIV, drug treatment or opportunistic infections. Antiretroviral drug therapy may itself cause serious complications (Fig. 21.6).

Other retroviral infections, especially with HTLV-1, also cause human disease. HTLV-1 infection may be acquired by sexual contact. It is associated with the later development of T-cell lymphoma and leukaemia, often with hypercalcaemia, and with a slowly progressive neurological syndrome characterized by a progressive spastic paraparesis (tropical spastic paraparesis). These syndromes occur in regions where HTLV-1 infection is endemic, such as central Africa, the Caribbean and parts of Asia.

Systemic examination

Particular attention should be paid to the skin, mouth, eyes, joints and, in late syphilis, the cardiovascular and nervous systems.

Special investigations

Cleanse the urethral meatus with a swab. If there is no visible discharge, gently milk the urethra forward from the bulb and note any discharge. A platinum or plastic bacteriological loop is inserted 1-2 cm into the urethra, proximal to the fossa navicularis, and the urethral material obtained is spread thinly on a glass slide for Gram staining. Endourethral material for gonococcal culture is placed directly onto a suitable culture plate or sent to the laboratory in modified Stuart’s transport medium. Positive cultures are tested for antimicrobial sensitivities and β-lactamase production.

Nucleic acid amplification tests (NAAT) using polymerase chain reaction (PCR), strand displacement assay (SDA) or transcription-mediated amplification (TMA) assay for chlamydia are more sensitive and can use urine instead of an endourethral specimen. NAAT can also be used to detect gonorrhoea.

Gram staining

The Gram-staining procedure is outlined in Box 21.4. If the patient has passed urine just before the test, the urethral smear may show no polymorphonuclear leukocytes because the urine will have washed out the accumulated urethral material. In such cases, the patient should be asked to reattend for an overnight or late afternoon urethral smear after holding urine for 8 or more hours. Gram-negative intracellular diplococci, which appear as opposing bean-shaped cocci within polymorphonuclear leukocytes under the microscope (Fig. 21.8), suggest gonococcal urethritis. The presence of five or more polymorphonuclear leukocytes per high-power field (×1000 magnification) with a negative test for gonococci indicates non-gonococcal urethritis (Box 21.5). The term non-specific urethritis is used to describe urethritis when specific causes, including Chlamydia trachomatis, Mycoplasma genitalium, trichomoniasis and non-sexually transmitted diseases such as bacterial urinary tract infection, have been excluded. However, the exclusion of C. trachomatis or M. genitalium infection requires specific and sensitive tests. A wet preparation, made by mixing urethral material using a loop with a drop of normal saline on a slide, can be examined by bright- or dark-field illumination for Trichomonas, which appear as ovoid protozoa with beating flagellae and in jerky motion. Continuing symptomatic urethritis a week or more after successful treatment for gonorrhoea indicates that the patient has postgonococcal urethritis, a non-gonococcal urethritis unmasked following treatment for gonorrhoea.

Genital ulcer

To investigate the cause of a genital ulcer, first cleanse the base of the ulcer with normal saline, and then gently squeeze it until a drop of serum exudes. Catch the exudates on the edge of a cover slip. Place this on a glass slide and press down firmly between filter paper. Examine the slide under dark-field microscopy for the characteristic morphology and movements of Treponema pallidum (Fig. 21.9) – bending itself at an angle, rotating forward on its long axis or alternating between contraction and expansion of its coils. Dark-field examination should be repeated for several days if syphilis is suspected.

Sometimes dark-field microscopy of suspected syphilitic ulcers may be negative, particularly if the patient has used a topical antiseptic or antibiotic cream. If regional lymph nodes are enlarged, a lymph node aspiration can be performed. After infiltration of the skin with 1% lidocaine, 0.2 ml of normal saline is injected into the node, the needle tip moved around in the node and then the saline aspirated. A drop is placed between a glass slide and cover slip, pressed between filter paper and examined under the dark-field microscope. In oral chancres, commensal treponemes from the gum margins may be confused with Treponema pallidum: because of this, immunofluorescent staining for pathogenic treponemes of serum from the ulcer, air-dried on a slide, is advisable. However, dark-field examination can be performed from oral ulcers away from the gum margin.

If anogenital herpes (Fig. 21.10) is suspected, the base of the blister or ulcer is swabbed and the swab sent for herpes simplex virus PCR, or placed in a viral transport medium for herpes culture. The diagnosis of donovanosis is based upon the demonstration of Donovan bodies, which stain in a bipolar fashion giving a ‘safety pin’ appearance within the cytoplasm of mononuclear cells in a Giemsa-stained tissue smear. Tissue is obtained by infiltrating the edge of the ulcer with 1% lidocaine and removing a small piece from the edge, which is then smeared onto a glass slide or crushed between two glass slides. If chancroid or lymphogranuloma venereum is suspected, culture or NAAT for Haemophilus ducreyi and Chlamydia trachomatis of the lymphogranuloma venereum serovars, respectively, may be indicated using material obtained from the ulcer or bubo.

Serological tests for syphilis

There are two groups of serological tests for syphilis:

The titre of the non-specific tests indicates disease activity and is useful for following up patients, particularly those who have been treated for primary, secondary or early latent syphilis, when the test should become negative or sustain a greater than two-fold dilution or four-fold decrease in antibody titre within 6-12 months. After successful treatment of all stages of syphilis, the specific tests usually remain positive whereas the VDRL or RPR test may slowly revert to negative, but commonly remains positive in lower titre in late syphilis. A greater than two-fold dilution or four-fold increase in antibody titre following treatment indicates recrudescence or reinfection.

The presence of a positive VDRL or RPR test on two occasions with negative specific tests and the absence of any evidence of treponemal disease indicate a biological false positive reaction. Acute false positive reactions may be due to acute febrile infections such as pneumonia, malaria, HIV infection and infective endocarditis, pregnancy and vaccination; they last less than 6 months. Chronic false positive reactions may indicate autoimmune diseases such as systemic lupus erythematosus, but can also occur in antiphospholipid syndrome, intravenous drug abusers, lepromatous leprosy and old age.

All patients should be screened for syphilis with serological tests using the treponemal EIA, TPPA or TPHA or combination of the VDRL/RPR and TPHA/TPPA. A positive EIA is confirmed with TPPA or TPHA (and vice versa) and a VDRL/RPR performed to assess activity. LIA or FTA-abs is used as the final ‘arbiter’ when there are discordant results between EIA and TPPA/TPHA. FTA-abs is being superseded by LIA. If syphilis is endemic, these tests should be repeated after 3 months if initial tests are negative. If primary syphilis is suspected, the EIA-IgM or FTA-abs IgM test is also performed, as this can be the first serological test to be positive, although any one or combination of treponemal tests may be positive. In babies with suspected congenital syphilis, the EIA-IgM or FTA-abs tests using an IgM conjugate should be requested because of passive transfer of maternal IgG antibodies across the placenta. When treponemes cannot be demonstrated, positive serological results must be confirmed by a second set of tests, but treatment should be started immediately in early infectious syphilis, or in pregnant women while awaiting confirmation.

Endemic treponematoses, such as yaws, bejel and pinta, may result in positive serological tests for syphilis. It is not possible to differentiate the treponematoses by serological tests. Patients may recall having such infection, or there may be a history of being brought up in the countryside in endemic areas, with evidence of signs of such infection, such as ‘tissue-paper’ scarring of the shins in yaws, which may suggest non-venereal treponematoses. However, there may be coinfection with syphilis, and it would be prudent to treat all positive treponemal serology as for syphilis.

Investigations for HIV infections

Screening for antibody to HIV, the causal agent for AIDS, is advisable for patients at risk of infection because of the possibility of early intervention with anti-HIV agents, preventative treatment against opportunistic infections such as Pneumocystis pneumonia, and the prevention of transmission from mother to child. The latter is achieved by treating both mother (antepartum, during labour and at delivery) and baby at birth with antiretroviral, caesarean section and avoidance of breastfeeding. The test may also be indicated to confirm or exclude HIV infection as a cause of immunosuppression or problematic medical illness. Consent from the patient for the test to be carried out, with information regarding the test, is desirable. The test should be repeated at 3 months to cover the ‘window’ period for incubating infection although 4th generation test (include both the HIV antibody and P24 antigen) can be positive by 6 weeks. HIV-RNA viral load testing can also be performed for patients suspected of acute HIV infection, as the HIV antibody test may initially be negative. Immunological assessment must include analysis of lymphocyte subtypes, especially CD4 and CD8 counts: a selective reduction in the numbers of circulating CD4 cells is characteristic of the disturbed immune state. The HIV-RNA test and the CD4 T-lymphocyte count are prognostic indicators of HIV infection and can be used to monitor progression as well as treatment efficacy. Other investigations will depend on the suspected systems involved. Patients with headache or neurological signs should first have a computed tomography or magnetic resonance imaging brain scan to exclude intracerebral lesions before a lumbar puncture is performed. HIV genotypic or phenotypic resistance tests are helpful in deciding on the choice of antiretroviral regimen in treatment-naïve patients, or in those who are failing treatment.