| INFECTIONS IN PREGNANT WOMEN | | | | A routine test done in every pregnant woman |
| Role of Diagnostic Microbiology | | | | irrespective of consent is associated with biological |
| Dr. T.V.RAO M.D | | | | false positives. Every positive test should be |
| DEPARTMENT OF MICROBIOLOGY | | | | reconfirmed testing with TPHA, a specific test to |
| Pregnancy is a dynamic state of health and disease, | | | | detect active infection. Testing with FTAbs IgG |
| shared by the pregnant woman and a growing fetus, | | | | remains the best option before diagnosis of syphilis is |
| a concern to the treating physician for timely | | | | ruled out. |
| diagnosis and necessary interventions. Infections with | | | | BACTERIAL INFECTIONS IN PREGNANT WOMEN |
| Viral, Bacterial, Parasitic and Fungi do occur in any | | | | Many bacterial infections have Major effect on |
| pregnant woman like other non pregnant woman of | | | | women’s health with implications on the New |
| similar age. Most infections are not serious. But some | | | | born. |
| infections are more important in pregnant woman | | | | URINARY TRACT INFECTIONS |
| than in non pregnant woman because of the potential | | | | Urinary tract infections remain the most common |
| for vertical transmission to foetus or infant. There is | | | | infections at any stage of pregnancy. Many present |
| a growing awareness on HIV, HBV, CMV, Rubella and | | | | with asymptomatic infections, Asymptomatic |
| Toxoplasmosis, on rare occasions Varicella and | | | | bactenuria which can only be identified on culturing |
| Listeriosis can do harm to the growing foetus. With | | | | the urine. It is ideal to order culturing in early |
| advances in medical treatments and laboratory | | | | pregnancy to be followed upto the last trimester of |
| technologies we are more concerned with | | | | pregnancy. Most neglected part of urine culturing |
| transmission of HIV, and HBV as we can still interfere | | | | remains with proper collection of specimen and often |
| with appropriate treatments. Now it is certain, every | | | | left to an inexperienced nursing staff. The treating |
| pregnant woman needs a successful screening for | | | | physicians should instruct the staff how to collect a |
| Rubella IgG, HBV surface antigen, and HIV antibodies | | | | mid stream and a clean catch sample. Less |
| apart from existing protocol for screening for Syphilis | | | | experienced Microbiologists give confusing reports but |
| in all pregnant women with VDRL / RPR testing. | | | | should not forget to specify the validity of report. A |
| WHY GOOD CLINICAL MICROBIOLOGY SERVICES | | | | cut off point of ? 100,000 bacteria/ml is the minimal |
| ARE IMPORTANT | | | | criteria in healthy pregnant women with isolation of a |
| No laboratory test for diagnosing a specific disease | | | | single species e.g. E.coli, Klebsiella species will |
| should be undertaken on a casual testing basis | | | | strengthen the diagnosis of urinary tract infections. |
| without knowing the implication of a positive value of | | | | Missing of asymptomatic bacteriuria can cause |
| test. Women are more willing to accept routinely | | | | premature labor and pylonephritis in pregnant women. |
| offered testing as in screening for syphilis with. The | | | | GROUP-B STREPTOCOCCAL INFECTION |
| situations to screen for antibodies to HIV turn to be | | | | There is a growing awareness on infections with |
| entirely different and needs an informed consent, as | | | | Group B Streptococci. CDC advices culturing for |
| every woman has a right to refuse any medical | | | | Streptococcus B group at 35-37 weeks of pregnancy |
| investigation or treatments. | | | | is important which can help to prevent early neonatal |
| UNDERSTANDING MICROBIOLOGY REPORTS WITH | | | | infection particularly premature labor. Appropriate |
| IMPLICATIONS ON FETAL HEALTH | | | | collection of specimen from cervix remains the |
| There is an unlimited gap of understanding between | | | | minimal requirement. |
| the laboratory reports and the treating physician, | | | | GONOCOCCAL AND CHLAMYDIAL INFECTION |
| which should be always brought down for improving | | | | They need specific or specialized techniques for |
| our quality of services. | | | | precise diagnosis but only ordered in high risk group |
| 1. All requests for any particular serological or | | | | of women as they can lead to pelvic inflammatory |
| molecular testing should be based on clinical | | | | diseases. The physician should discuss with clinical |
| symptoms (May not necessary as in HIV, HBV, CMV | | | | microbiologist as routine testing is not possible in less |
| and Syphilis which are symptom free in early stages.) | | | | equipped laboratories and will not serve the purpose |
| 2. Writing a good clinical history will certainly guide the | | | | BACTERIAL VAGINOSIS AND CANDIDIAL |
| testing clinical microbiologist to use the right protocol | | | | INFECTIONS |
| in the laboratory methods.eg. Toxoplasmosis, CMV, | | | | There is a growing incidence of Gardnernella vaginalis |
| Rubella to determine the active infection. | | | | and Candidial infection. Few laboratories have |
| INTERPRETATION OF RESULTS RUBELLA, CMV, | | | | adequate facilities for characterization of etiological |
| TOXOPLASMOSIS, VARICELLA Infections. | | | | agents. The clinical requests should specify what they |
| 1. Clinicians should request for IgG in all cases apart | | | | are looking for. |
| from IgM which is only positive in recent infections. | | | | Today we have an ever growing list of microbes |
| 2. Best serological evidence of recent infections is | | | | including Varicella, Herpes simplex, Parvovirus B19, |
| IgG seroconversion (a change from a negative test | | | | Listeriosis and many others encroaching on pregnant |
| to positive test) to understand all serological tests | | | | women. An appropriate investigation and |
| which turn out to be negative on first testing, do not | | | | management can reduce adverse outcome, |
| exclude recent infections. Testing should be repeated | | | | unnecessary interventions and anxiety. The need of |
| upto three weeks after suspected contact, which | | | | the hour in up gradation of our Microbiology |
| may be extended up to 6 months in cases of | | | | laboratories to cope, with changing trends in infection |
| diagnosis of HIV Infection for appearance of | | | | as there is ever-increasing list of Microbes harming a |
| antibodies. | | | | pregnant women and the growing fetus. |
| 3. When a specific IgM is positive without IgG being | | | | CAUTION ON MOLECULAR METHODS |
| positive results should be interpretated with caution. | | | | All molecular methods for diagnosis of infectious |
| If Ig G seroconversion do not occur the IgM result is | | | | diseases ordered with caution. It is ideal to try all time |
| likely to be a false positive | | | | tested laboratory methods and to consider the using |
| 4. The question comes how recent is infection: can | | | | of molecular methods which on many occasions are |
| be clarified with newer generation of serological | | | | research or academic tools with good number of |
| testing in accredited laboratories. The clinicians should | | | | false positive reactions. |
| ask for IgG avidity assays which will help confirm or | | | | In spite of several advances in Laboratory |
| exclude recent infection. ( Eg , Toxoplasmosis, Rubella | | | | Technologies in Developing countries, we in India |
| and CMV ) As high avidity indicates that infection | | | | must depend on the wisdom of our Physicians, as |
| occurred several months previously. Interpretation | | | | our patients do not afford many investigations on |
| depends on laboratory protocols and should be | | | | random basis or for Academic interest. However, |
| discussed with clinical microbiologists. | | | | antenatal screening that is not based on accepted |
| HIV SCREENING OR TESTING | | | | criteria or well defined plan of action can cause |
| The problems of screening all pregnant women for | | | | unnecessary anxiety and potentially dangerous |
| HIV antibody is a complex issue. It should be | | | | intervention. Still we know little how a Fetus protects |
| discussed and issue can be still be resolved if offered | | | | and survives itself in spite of several challenges apart |
| as testing with motive of offering antiretroviral | | | | from Infections. |
| therapy to both mother and new born if infected. | | | | Email; tvraodoctor2000@yahoo.co. |
| SCREENING FOR SYPHILIS (WITH VDRL/RPR) | | | | |