Introduction The family Chlamydiaceae, obligate intracellular bacteria, is comprised of four species: C. trachomatis, C. pneumoniae, C. psittaci and C. pecorum, which cause many types of diseases. Species are divided according to host range, biochemical, biologic, and molecular properties1. C. trachomatis has 15 serovars which are divided into the trachoma serotypes A-C, the occulo- genital serovars D-K, and the lymphogranuloma
venerum (LGV) serovars L -L (Table1). The
serovars can be distinguished by serological
typing which uses monoclonal antibodies or by
Species of Chlamydiae and the diseases with whichSpecies Disease Sequelae or Chronic Disease C. trachomatis is the etiologic agent of a
RB utilizies the host nutrient resources and
wide variety of diseases. Trachoma is a sequela
adenosine triphosphate (ATP) for its energy
of ocular disease in developing countries and
source to divide by binary fission within the
continues to be a leading cause of preventable
inclusion body of the infected cell. This
blindness. Urogenital, ocular, and pneumonic
phagosome resists fusion with host lysozymes,
infections are caused by the serovars D-K. The
thus allowing the chlamydia to evade destruction
urogenital infections are sexually transmitted and
by the host cell. In 48-72 hours, at the end of
may be transmitted to infants born to infected
the life cycle, the RBs condense back to EBs,
the inclusion body and cell rupture to release
neonatal pneumonia. C. pneumoniae, exclusively
new infective EBs, and the life cycles continues.
a human pathogen thus far, has been associatedwith respiratory diseases, including pneumonia. Epidemiology and Diseases
Antibody prevalence studies demonstrate that it
There is a heavy burden of disease for society
is highly prevalent in man, with approximately
due to chlamydial diseases world wide. It is
50% or more of adults having antibodies to the
estimated that there are 7 million cases of
organism. It has recently been associated with
blindness worldwide due to scarring from
trachoma with as many as 500 million active
C. psittaci is the cause of psittacosis in
cases of trachoma.1 The remainder of this
psittacine and nonpsittacine birds, including
report focuses on urogenital infections and
parrots, canaries, turkeys, pigeons, and ducks, as
their sequelae caused by C. trachomatis.
well as in other animals such as cats, cattle, and
C. trachomatis infections are among the most
sheep. Man can be an accidental host, infected
common sexually transmitted diseases among
through aerosolized droplet transmission to the
young adults and adolescents.3, 4 More than 50
respiratory tract from infected birds or animals,
million cases occur worldwide and approximately
4 million cases occur in the United States,
C. pecorum, a recently described species, is
annually.3, 4 Chlamydia infections are associated
a pathogen of ruminants, but has never been
with many clinical syndromes ranging from
cervicitis, salpingitis, acute urethral syndrome,endometritis, ectopic pregnancy, infertility, and
pelvic inflammatory disease (PID) in the female;
Chlamydiae have an unusual intracellular life
conjunctivitis and pneumonia in infants born to
cycle compromised of two unique forms, the
infected mothers; and urethritis, proctitis, and
elementary body (EB), which is infectious but not
epididymitis in the male.5-7 Because of the
metabolically active, and the reticulate body (RB),
seriousness of the sequelae of infections, women
which is noninfectious but is metabolically active.
bear the most morbidity of chlamydia infections.
After the intracellular EB becomes an RB, the
Untreated chlamydia infections lead to PID and
multiple episodes of PID can lead to tubal factor
RECOMMENDED REGIMENS
infertility.8-11 Unfortunately, symptoms of genitalinfection are often completely absent or very
Azithromycin 1 gram orally in a single dose
mild among infected patients, especially women,
creating a large reservoir of infected persons who
Doxycycline 100 mg orally twice a day for 7 days
continue transmission to new sexual partners.12
s ALTERNATE REGIMENS
Chlamydial infections occur primarily among
young sexually active persons. Prevalence rates
Erythromycin base 500 mg orally 4 times a day
geographical areas, and may range from 5-20%
Erythromycin ethylsuccinate 800 mg orally 4 times
in various groups of young adults.7, 13 Because
symptoms are absent in most infected individuals,
these prevalences may be severely underesti-
Ofloxacin 300 mg orally twice a day for 7 days
mated. Thus, widespread screening of individualsat greatest risk (e.g., those individuals who areyoung, sexually active, and have new or multiple
Impact on Society
In many societies, especially in the developing
world, infertility, which may result from untreatedchlamydia infections, poses a severe psychological
For uncomplicated genital infections, such as
burden upon women who may be stigmatized by
mucopurulent cervicitis in women and urethritis
their community or shunned by their husbands.
or nongonococcal urethritis in men, caused by
Untreated or undiagnosed ectopic pregnancies
C. trachomatis, doxycycline has been the most
widely used antichlamydial therapy in previous
The serious complications and sequelae of
years. However, single dose azithromycin is now
untreated chlamydia infections also pose a
highly recommended because of its excellent
significant economic burden on health care costs.
tissue penetration, its long half life of 5-7 days,
Approximately one million cases of symptomatic
and lack of concern of compliance.14 Treatment
PID are diagnosed annually in the United States,
should begin as soon as possible after diagnosis.
leading to 100,000 surgeries and over 275,000
For more persistent infections and complications
hospitalizations a year.15, 16 The annual estimated
such as pelvic inflammatory infection, the reader
cost associated with the sequelae of ectopic
is referred to the new Centers for Disease Control
pregnancy and infertility may exceed five billion
and Prevention’s 1998 Guidelines for the Treatment
of Sexually Transmitted Diseases publication.14
Cost-effectiveness studies, utilizing computer
Patients should be encouraged to refer their sex
modeling and decision tree analyses, have
partners for evaluation, testing, and treatment.14
recently been reported, which indicate that it is
DNA amplified technology that culture may have
more cost-effective to screen and treat infected
a sensitivity ranging from 50-85%, depending
women than for society to bear the financial
burden imposed later due to the medical costs
associated with the sequelae diseases such as
Because older non-culture tests, such as DFA
pelvic inflammatory disease, ectopic pregnancy,
and EIA, were traditionally compared to culture
as a gold standard, the sensitivities reported inthe older literature can no longer be viewed asaccurate. A recent meta-analysis which adjusted
Diagnostic Tools for Detection
the sensitivities of such assays based on a
of Chlamydia Infections
sensitivity of culture of 85% has been reported.48
Previously, detection of chlamydia has been
Table 2 shows a comparison of the sensitivities
accomplished either by 1) staining of chlamydial
and specificities of diagnostic assays available
inclusions grown in tissue culture cells,20 2) direct
for the detection of C. trachomatis in clinical
examination of patient clinical specimens for the
detection of elementary bodies using monoclonalantibodies or direct fluorescent antibody (DFA)
staining,21-23 3) antigen detection in enzyme immunoassay (EIA)24-27 or 4) nucleic acid probe Sensitivity and specificity of diagnostic tests for thedetection of C. trachomatis*
hybridization.28-30 Now, new molecular technologies are available that amplify the DNA
Diagnostic Method Sensitivity Specificity
of chlamydia in clinical specimens,31-47 which offer greatly expanded sensitivities of detection,
while maintaining high specificity. Although
serological tests for diagnosis of chlamydia
infections, such as complement fixation or
microimmunofluorescence, are still used for diagnosis of C. psittaci and C. pneumoniae, they
are not useful for the diagnosis of C. trachomatis.
epidemiological surveys to associate previous
C. trachomatis infection with infertility or
Whereas culture was previously thought to be
the gold standard for the detection of chlamydia
*Sensitivities and specificities adapted from a modified meta-analysis
in clinical specimens, it can now be shown
of published papers, reference #48 (Howell, M.R. et al. Sex.
because of the expanded sensitivity capability of
New Specimen Types Available
these include: schools, prisons, military reception
for the Detection of C. trachomatis
stations, health vans, shopping malls, and even
New nucleic acid (DNA or RNA) amplification
technology is so powerful that fewer than 10 elementary bodies can be detected in clinical
Screening Strategies
specimens and theoretically even one can serve
There is recent evidence that screening and
as a target for amplification. Because of this
treatment can prevent the sequelae of pelvic
improved sensitivity of detection, alternative
inflammatory disease (PID) often associated
specimen types have been found to be useful
with undiagnosed chlamydia infections. In a
for chlamydia diagnosis. First-void urine from
prospective clinical trial conducted within a large
health maintenance organization, the group of
amplification tests with great accuracy. Because
urines are easily obtained, non-invasive
treatment for chlamydia infections developed
specimens, they offer a great advantage for
60% fewer cases of PID within a one year
large public health screening programs, where
follow-up period than did those women who
there is no opportunity to obtain a cervical or
were control subjects and were not offered
urethral specimen. Additionally, urine specimens
are highly acceptable to individuals who may be
asymptomatic and who are unwilling to submit to
chlamydia screening programs have been in
a medical examination. Because a clinician is not
effect for a number of years, such as the Pacific
required for urine collection, cost savings are also
Northwest and Wisconsin, for example, the rates
generated when screening large numbers of
for chlamydia prevalence in the Centers for
Disease Control and Prevention supported clinics
have steadily declined from prevalences of about
shown to be both sensitive and specific for the
13% to less than 5%. In Scandanavian countries,
detection of chlamydia when amplified tests are
which have had chlamydia control programs in
used and which has high acceptability by the
place for many years, rates are below 3%.
female patient is a self-administered vaginal or
In choosing target populations for chlamydia
screening programs, public health clinicians will
Although sexually transmitted disease clinics
want to concentrate on populations which have
and family planning clinics have been the source
the most disease and are at most risk for the
of specimens for chlamydia screening programs,
development of sequelae. These populations
usefulness of alternative specimen types has
are mostly the young, sexually active females.
made alternative sites for screening programs
Adolescents in schools and those young women
attractive to public health officials. Some of
who attend prenatal and family planning clinics
are especially important to include in addition to
screening program or because an examination is
the more traditional sexually transmitted disease
not indicated, clinicians should take advantage of
clinics. Underserved populations such as youth
the ease of obtaining a urine specimen or even a
in detention centers, prostitutes, and homeless
self-administered vaginal swab for amplification
persons in shelters are important populations for
testing. For male patients, the urine specimen is
screening also. Treatment of partners to prevent
usually always the choice of specimen for testing
reinfection of patients is an important issue and
for chlamydia with an amplification assay. DNA
can be easily addressed with the use of urine
amplification tests should not be used for test of
cure assays until 3 weeks after therapy because
residual DNA from cells rendered non-infective
amplification-based screening technology is the
by antibiotics may give a positive test when the
ability to use the same specimen for the same
type of diagnostic assay for other sexually
One study which examined incidence rates in
transmitted diseases such as gonorrhea. Many
adolescents has shown that the young may get
studies have shown that coinfection with both
reinfected with chlamydia as frequently as every
chlamydia and N. gonorrhoeae are common in
6 months on average.55 Studies have also shown
sexually active individuals and more evidence is
that individuals who practice high risk sexual
behaviors, such as new or multiple sex partners
infections are more common than previously
or who do not use condoms, are at greater risk
for chlamydia infections.19, 56-58 Therefore, asymptomatic patients who meet any of these
Choice of Diagnostic Test and
criteria should be screened every time they are incontact with a health care facility or screening
Specimen for Screening
situation with the use of a non-invasive
Even though molecular amplification assays are
generally more expensive than older non-culturetests such as DFA, EIA, and probe assays, cost
effectiveness assays, which are done from a societal perspective, have been shown to be
Clinicians now have a new type of test for thedetection of chlamydial infections which is a new
more cost-effective.48 If a female patient has
gold standard that is more sensitive for the
urogenital symptoms or if a pelvic examination is
detection of chlamydia than culture and other
being performed on a patient, clinicians should
non-culture tests. The nucleic acid amplification
obtain a cervical swab for a nucleic acid amplified
tests, which amplify chlamydial DNA or RNA in a
test, because cervical swabs have the highest
clinical specimen, are so powerful that they can
sensitivity. If a patient or individual is not
be also used with urine specimens and even
receiving a pelvic examination, such as in a
self-administered vaginal swabs. The use of such
tests offers clinicians and public health officials a
8. Westrom LV. Sexually transmitted diseases
cost-effective way to control a highly prevalent
disease which causes serious morbidity and a
9. Westrom L. Effect of pelvic inflammatory
References
Peeling RW, Brunham RC. Chlamydiae as
10. Hillis SD, Joesoef R, Marchbanks PA,
Delayed care of pelvic inflammatory disease as a risk factor impaired fertility. Am J Obstet
Gaydos CA, Quinn TC, et al. Isolation of Chlamydia pneumoniae from the coronary
11. Hillis SD, Wasserheit JN. Screening for
Chlamydia a key to the prevention of pelvic
inflammatory disease. N Engl J Med 1996;
3. Centers for Disease Control and Prevention.
12. Quinn TC, Gaydos C, Shepherd M, Bobo L,
Hook III EW, Viscidi R, et al. Epidemiologic
management of Chlamydia trachomatis
and microbiologic correlates of Chlamydia trachomatis infection in sexual partnerships. JAMA 1996; 276:1737-1742.
4. Quinn TC, Cates W. Epidemiology of sexually
transmitted diseases in the 1990’s. In: Quinn
13. Stamm WE. Diagnosis of Chlamydia trachomatis genitourinary infections. Ann
14. Centers for Disease Control and Prevention.
1998 guidelines for treatment of sexually
transmitted diseases, pelvic inflammatory
disease, and infertility: an epidemiologic
update. Epidemiol Rev 1990; 12:199-220.
15. Centers for Disease Control. Policy guidelines
6. Gaydos CA. Chlamydia trachomatis
infections. Resid Staff Phys 1993; 17-22.
pelvic inflammatory disease (PID). MMWR 1991; 40 (RR-5):1-25.
7. Stamm WE, Holmes KK. Chlamydia trachomatis infections of the adult. In:
16. Cates JW, Rolfs RT, Aral SO. Sexually
Holmes KK, Mardh PA, Sparling PF, Wiesner
transmitted diseases, pelvic inflammatory
PJ, editors. Sexually Transmitted Diseases.
disease, and infertility: an epidemiologic
New York, NY: McGraw-Hill Co, 1990:181-193.
update. Epidemiol Rev 1990; 12:199-220.
17. Westrom L, Joesoef R, Reynolds G, Hagdu A,
Thompson SE. Pelvic inflammatory disease
and fertility: a cohort study of 1,844 women
24. Clark A, Stamm WE, Gaydos C, Welsh L,
with laparoscopically verified disease and
Quinn TC, Schachter J, et al. Multicenter
657 control women with normal laparoscopic
evaluation of the antigEnz chlamydia enzyme
results. Sex Transmit Dis 1992; 19:185-192.
immunoassay for diagnosis of Chlamydia
18. Howell MR, Quinn TC, Gaydos CA. Screening
trachomatis genital infection. J Clin
for Chlamydia trachomatis in asymptomatic
women attending family planning clinics:
25. Gaydos C, Reichart C, Long J, Welsh L,
Neumann T, Hook EW, et al. Evaluation of
preventive strategies. Ann Intern Med 1998;
Chlamydia trachomatis in genital specimens.
19. Marrazzo JM, Celum CL, Hillis SD, Fine D,
J Clin Microbiol 1990; 28:1541-1544.
DeLisle S, Handsfield HH. Performance and
26. Sanders JW, Hook EW, Welsh LE, Shepherd
cost-effectiveness of selective screening
criteria for Chlamydia trachomatis infection
immunoassay for detection of Chlamydia trachomatis in urine of asymptomatic men.
chlamydia control strategy. Sex Transmit Dis
27. Chan EL, Brandt K, Horsman GG. A 1-year
20. Centers for Disease Control. Laboratory
evaluation of Syva MicroTrak Chlamydia
Update: Isolation of Chlamydia trachomatis
confirmation by direct fluorescent-antibody
assay in a high-volume laboratory. J Clin
21. Taylor HR, Agarwala N, Johnson SL.
Detection of experimental Chlamydia
28. Clarke LM, Sierra MF, Daidone BJ, Lopez N,
trachomatis eye infections in conjunctival
fluorescein-conjugated monoclonal antibody.
and Gen-Probe PACE 2 with cell culture for
diagnosis of cervical Chlamydia trachomatis
22. Uyeda CT, Welborn P, Ellison-Birang N, Shunk
K, Tsaouse B. Rapid diagnosis of chlamydial
infections with the MicroTrak direct test.
29. Warren R, Dwyer B, Plackett M, Pettit K, Rizvi
23. Lidner LE, Geerling S, Nettum JA, Miller SL,
Altman KH, Wechter SR. Identification of
detection assays for Chlamydia trachomatis.
J Clin Microbiol 1993; 31:1663-1666.
immunofluorescence: technique, sensitivity,
30. Stary A, Teodorowicz L, Horting-Muller I,
Chlamydia trachomatis in urogenital
samples. Sex Transmit Dis 1994; 21:26-30.
31. Jaschek G, Gaydos C, Welsh L, Quinn TC.
reaction assays for detecting Chlamydia
Direct detection of Chlamydia trachomatistrachomatis nucleic acids. J Clin Microbiol
38. Bass CA, Jungkind Dl, Silverman NS, Bondi
JM. Clinical evaluation of a new polymerase
J Clin Microbiol 1993; 31:1209-1212.
32. Bobo L, Coutlee F, Yolken RH, Quinn T,
Chlamydia trachomatis in endocervical
Viscidi RP. Diagnosis of Chlamydia trachomatis cervical infection by detection of
amplified DNA with an enzyme immunoassay.
39. Quinn TC, Welsh L, Lentz A, Crotchfelt K,
J Clin Microbiol 1990; 28:1968-1973.
Zenilman J, Newhall J, et al. Diagnosis by
Amplicor PCR for Chlamydia trachomatis
Detection and differentiation of Chlamydia
infection in urine samples from women and
trachomatis, C. psittaci, and C. pneumoniae
men attending sexually transmitted disease
by DNA amplification. J Infect Dis 1990;
clinics. J Clin Microbiol 1996; 34:1401-1406.
40. Dille BJ, Butzen CC, Birkenmeyer LG.
34. Loeffelholz MD, Lewinski CA, Silver SR,
Amplification of Chlamydia trachomatis DNA
Purohit AP, Herman SA, Buonagurio DA, et
by ligase chain reaction. J Clin Microbiol
al. Detection of Chlamydia trachomatis in
endocervical specimens by polymerase chain
41. Gaydos CA, Jang D, Welsh LE, Pare B,
Chernesky MA, Sellors J, et al. Ligase chain
reaction (LCR): a novel DNA amplification
35. Bauwens JE, Clark AM, Loeffelholz MJ,
technique for Chlamydia trachomatis (CT) in
Chlamydia trachomatis urethritis in men by
42. Schachter J, Stamm WE, Quinn TC, Andrews
first-catch urine. J Clin Microbiol 1993;
reaction to detect Chlamydia trachomatis
infection of the cervix. J Clin Microbiol 1994;
Diagnosis of Chlamydia trachomatis
43. Chernesky MA, Lee H, Schachter J, Burczak
genitourinary Chlamydia trachomatis
infections by using the ligase chain reaction
diagnosis of Chlamydia trachomatis urethral
on patient-obtained vaginal swabs. J Clin
infection in symptomatic and asymptomatic
men by testing first void urine in a ligase
50. Stary A, Chouieri B, Lee H. Implications of
sensitive molecular diagnosis of Chlamydia trachomatis in non-invasive sample types.
44. Chernesky MA, Jang D, Lee H, Burczak JD,
Eleventh Meet. Internat. Soc.STD Research
Chlamydia trachomatis infections in men
51. Scholes D, Stergachis A, Heidrich FE, Andrilla
and women by testing first-void urine by
ligase chain reaction. J Clin Microbiol 1994;
pelvic inflammatory disease by screening for
cervical chlamydial infection. N Engl J Med
45. Bassiri M, Hu HY, Domeika MA, Burczak J,
Svensson LO, Lee HH, et al. Detection of
52. Burstein G, Waterfield G, Joffe A, Zenilman J,
Chlamydia trachomatis in urine specimens
from women by ligase chain reaction. J Clin
amplification in adolescents attending middle
Burczak JD, Andrews WW, Muldoon S, et al.
Diagnosis of Chlamydia trachomatis
53. Gaydos CA, Crotchfelt KA, Howell MR,
genitourinary infection in women by ligase
Kralian S, Hauptman P, Quinn TC. Molecular
chain reaction assay of urine. Lancet 1995;
amplification assays to detect chlamydial
47. Gaydos CA, Ngeow YF, Lee HH, Canavaggio
school female students and to monitor the
M, Welsh L, Johanson J, et al. Urine as a
persistence of chlamydial DNA after therapy.
diagnostic specimen for the detection of
Chlamydia trachomatis in Malaysia by ligase
54. Workowski KA, Lampe MF, Wong KG, Watts
Chlamydia trachomatis genital infection after
48. Howell MR, Quinn TC, Brathwaite W, Gaydos
CA. Screening women for Chlamydia trachomatis in family planning clinics: the
55. Burstein G, Gaydos CA, Diener-West M,
Howell MR, Zenilman J, Quinn TC. Incident
assays. Sex Transmit Dis 1998; 25:108-117. Chlamydia trachomatis infections among
49. Hook III EW, Smith K, Mullen C, Stephens J,
inner-city adolescent females. JAMA 1998;
Rinehart L, Pate M, Lee HH. Diagnosis of
56. Marrazzo JM, White CL, Krekeler B, Celum
CL, Lafferty WE, Stamm WE, et al. Community-based urine screening for Chlamydia trachomatis with a ligase chain reaction assay. Ann Intern Med 1997; 127:796-803.
Halloran EM. Predictors of Chlamydia trachomatis infection among female adolescents: A longitudinal analysis. Am J Epidemiol 1996; 144:997-1003.
58. Mosure DJ, Berman S, Fine D, DeLisle S,
Cates W, Boring III JR. Genital Chlamydia infections in sexually active female adolescents: Do we really need to screen everyone? J Adol Health Care 1997; 20:6-13. BD Diagnostic Systems 7 Loveton Circle Sparks, MD 21152-0999 800.638.8663 www.bd.com/clinical
BD, BD Logo and BDProbeTec are trademarks of Becton, Dickinson and Company. 2002 BD3-2384 September 2002 Printed in USA
Querstraße 2, 25451 Quickborn, Tel.: 04106/6470570 Bitte füllen Sie diesen Fragebogen genau aus. Bei den Beispielen genügt es zu unterstreichen sofern diese zutreffen; ansonsten bitte mit eigenen Worten beantworten. Bitte nehmen Sie sich genug Zeit. Alle Ihre Angaben unterliegen der Schweigepflicht. Gewicht _________ Größe _______ Temperatur_______ Blutdruck________ Puls__________(Temper
EIDGENÖSSISCHES DEPARTEMENT FÜR AUSWÄRTIGE ANGELEGENHEITENDÉPARTEMENT FÉDÉRAL DES AFFAIRES ÉTRANGÈRESDIPARTIMENTO FEDERALE DEGLI AFFARI ESTERI Personal pandemic preparedness Bird flu is currently an animal disease and only infects humans in isolated cases. It is impossible to predict if and when the avian flu virus now circulating will mutate into a pandemic virus. The course of an