This document discusses invasive and non-invasive methods used to monitor pregnancy and fetal health, including ultrasonography, cardiotocography, non-stress tests, and contraction stress tests. Non-invasive methods like ultrasounds and CTGs are used to examine the fetus and monitor heart rate and movements without entering the uterus. Invasive methods like amniocentesis and chorionic villus sampling collect cell or fluid samples by entering the uterus and carry risks of infection or miscarriage but can test for genetic conditions. Both invasive and non-invasive methods aim to monitor fetal growth and well-being, enable treatment of conditions, and inform parents of any health issues.
This document discusses invasive and non-invasive methods used to monitor pregnancy and fetal health, including ultrasonography, cardiotocography, non-stress tests, and contraction stress tests. Non-invasive methods like ultrasounds and CTGs are used to examine the fetus and monitor heart rate and movements without entering the uterus. Invasive methods like amniocentesis and chorionic villus sampling collect cell or fluid samples by entering the uterus and carry risks of infection or miscarriage but can test for genetic conditions. Both invasive and non-invasive methods aim to monitor fetal growth and well-being, enable treatment of conditions, and inform parents of any health issues.
This document discusses invasive and non-invasive methods used to monitor pregnancy and fetal health, including ultrasonography, cardiotocography, non-stress tests, and contraction stress tests. Non-invasive methods like ultrasounds and CTGs are used to examine the fetus and monitor heart rate and movements without entering the uterus. Invasive methods like amniocentesis and chorionic villus sampling collect cell or fluid samples by entering the uterus and carry risks of infection or miscarriage but can test for genetic conditions. Both invasive and non-invasive methods aim to monitor fetal growth and well-being, enable treatment of conditions, and inform parents of any health issues.
1. 1. NEWER MODALITIES OF PREGNANCY- INVASIVE AND NON INVASIVE
KHUSHBU PATEL GCS SCHOOL/COLLEGE OF NURSING 2. 2. INTRODUCTION • Many changes occur in woman’s body during pregnancy. These changes although most apparent in the reproductive organs, involve other body systems as well. • Weeks may pass before the family realizes she has become pregnant or she may learn upon a visit to a doctor for other reasons • Confirmation her pregnancy is most important for the health & welfare of herself & the baby. In this lesson, we will cover the tests used to determine pregnancy 3. 3. RISK APPROACH SCREENING • Blood testing • Excessive weight gain of the mother due to fluid retention. Falling weight also poses risk as there can be intrauterine growth retardation. • Pre-existing hypertension or PIH • Excess amount or decreased amount of amniotic fluid is another risk factor. • Other approaches, which should be followed for high-risk cases, are: non-invasive & invasive methods are used 4. 4. • Non-invasive methods: • Examination of the woman’s uterus from outside the baby. • Listening to the fetal heart sound • External fetal monitoring • It includes: Ultrasonography, • Cardiotocography, • Non- stress test, • Contraction stress test, • amniotic fluid index 5. 5. • Invasive methods: • Chorionic villus sampling • Amniocentesis • Fetoscopy • MSAFP: maternal serum alpha feto protein. • Others includes Cordocenthesis, Amnioscopy. 6. 6. OBJECTIVE OF INVASIVE & NONINVASIVE DIAGNOSIS • To reduce maternal and fetal mortality rate. • To check fetal growth and development. • To enable timely medical or surgical treatment of a condition before or after birth, • To give the parents the chance to abort a fetus with the diagnosed condition, • To give parents the chance to "prepare" psychologically, socially, financially, and medically for a baby with a health problem or disability, or for the likelihood of a stillbirth 7. 7. Common indicators of invasive & noninvasive diagnosis:- 8. 8. • 1) ULTRASONOGRAPHY • 2) CARDIOTOCOGRAPHY • 3) NON STRESS TEST • 4) CONTRACTION STRESS TEST • 5) AMNIOTIC FLUID INDEX (AFI) NON-INVASIVE METHODS OF DIAGNOSIS 9. 9. ULTRASONOGRAPHY (USG) • An ultrasonography is a diagnostic technique, which uses high-frequency sound waves to create an image of the internal organs. • A screening ultrasound is sometimes done during the course of a pregnancy to check normal fetal growth and verify the due date. • It is a safe , non invasive, accurate and cost effective investigation • Hard tissues such as bone appear white on the image and soft tissues appear grey. 10. 10. Indications: • In the first trimester: • To establish the dates of a pregnancy • To determine the number of fetuses and identify placental structures • To diagnose an ectopic pregnancy or miscarriage • To examine the uterus and other pelvic anatomy • In some cases to detect fetal abnormalities as anencephaly 11. 11. • Mid-trimester: (sometimes called the 18 to 20 week scan)to confirm pregnancy dates or gestational age • To determine the number of fetuses and examine the placental structures • To assist in prenatal tests such as an amniocentesis, Cordocenthesis . • To examine the fetal anatomy for presence of abnormalities • To check the amount of amniotic fluid by measuring AFI. • To examine blood flow patterns • To check on the location of placenta; to see if its covering cervix • To observe fetal behavior and activity 12. 12. • Third trimester: • To monitor fetal growth, to check IUGR • Detailed anatomical survey. • To check the amount of amniotic fluid • to determine the position of a fetus • To assess the placenta 13. 13. types of ultrasounds performed during pregnancy Abdominal ultrasound Transvaginal ultrasound 14. 14. Abdominal ultrasound • In an abdominal ultrasound, gel is applied to the abdomen and the ultrasound transducer glides over the gel on the abdomen to create the image 15. 15. TRANSABDOMINAL USG 16. 16. TRANSVAGINAL ULTRASOUND • a smaller ultrasound transducer is inserted into the vagina and rests against the back of the vagina to create an image. • A transvaginal ultrasound produces a sharper image and is often used in early pregnancy. 17. 17. TRANSVAGINAL USG 18. 18. • Indication of transvaginal ultrasound:- • Early month of pregnancy • In this high frequency of sound waves used so greater resolution is possible • Typical gynaecological indication includes uterine size, evaluation of endometrium, myometrium, cervix • Contraindication:- • Allergy to latex. • Vaginal infection 19. 19. Nursing responsibility before procedure • Explain the purpose of procedure and how it will be done. • Advise for drink lots of water so that full bladder to capture clearer images • Provide privacy. • Provide supine position . (dorsal position). • The abdominal wall is prepared and draped. • Check USG 20. 20. Procedure : • TRANS ABDOMINAL USG:- • Explain the procedure to the patient. • Provide privacy • Provide supine position to the patient. • Apply gel 21. 21. Transvaginal USG • A probe is placed into the vagina instead of over the abdomen. • Provide dorsal lithotomy position with empty bladder. • Vaginal probe should be lubricated with gel and the probe should be inserted in to an appropriate covering sheeth such as condom • The sheath covered probe is gently advanced up the vaginal canal • If ultrasound is done before the week 11, it would be transvaginal 22. 22. Safety of USG • Ultrasounds bring no long term or short-term harm to both mother and baby. • In fact, it is a useful scanning tool. Because the waves are of very low intensity, there is no danger in repeating the scans, if your condition merits it. • However if pregnancy is normal, then 2 routine scans as part of antenatal care. • More scans are only necessary if any medical condition 23. 23. Advantage of USG • Complex structure can be viewed in a single image. • Stored data can be reviewed at any plane later on without needing the patient, this helps to get second opinion if required. • Prenatal diagnosis of certain anomalies is improved. • Photo of 3- Dimensional image improves antenatal parental bonding and important teaching tool. 24. 24. CARDIOTCOGRAPHY • Cremer first demonstrates this method in 1904. In this test, Fetal Heart Rate and uterine contraction are graphically recorded. It is generally performed in third trimester. • The machine used to perform the monitoring FHR called a cardiotocograph or electronic fetal monitor or external fetal monitor 25. 25. CARDIOTOCOGRAPH 26. 26. CARDIOTOCOGRAPH 27. 27. Procedure 28. 28. • INTERPRETATION • A typical CTG output for a woman not in labour. A: Fetal heartbeat; B: Indicator showing movements felt by you (caused by pressing a button); C: Fetal movement; D: Uterine contractions 29. 29. Advantages:- • Help to detect hypoxia in early stage. • Reduce fetal death • It is important record for medico-legal purpose Drawback • Instrument is expensive and trained person are required to interpret. • Mother has to confined in bed • Due to false prediction caesarean section rate may be high 30. 30. Non-stress Test ( NST) • Non-stress test is a simple, painless procedure in which a baby's heartbeat is continuously monitored for 20 minutes or more along with recording fetal movement. • The logic behind the test is, that like adults, a baby's heartbeat should accelerate when it is active i.e. moving and kicking. • Principle : there is acceleration of fetal heart rate with each fetal movement 31. 31. Performing time:- • The Non-stress test can be done whenever the need arises so there is no specific time for it. around 30 weeks 32. 32. Indications of NST • Women with preexisting medical conditions such as diabetes. • Women with pregnancy-induced medical conditions such as hypertension • Baby is less active than normal • Baby is small for its age • Amniotic fluid is either too much or too little • Women who have previously lost their babies in the second half of their pregnancies • Women with pregnancies continuing after week 40 to basically check on the well- being of baby 33. 33. Nursing responsibility • Explain procedure before performing test. • Informed consent should be given prior to testing, and a woman has the right to refuse this test if she chooses • Provide lateral position or semi fowler or sitting position to the women. • the recording is obtained with the patient lie down on left side, or lateral recumbent position. ( to avoid supine hypotension) 34. 34. Procedure 35. 35. Contd… • Two electronic devices will be strapped to mother abdominal. • The transducer ultrasound will monitor baby's heartbeat. • The other device will record any uterine contractions felt by the mother. • While fetal movement is recorded by mother by pressing a button which makes the mark on the strip. • If there are no movements, the fetus is stimulated manually or may be with a buzzer • The test takes about 20 minutes to an hour 36. 36. Interpretation • Reactive test (normal NST) :- NST is called reactive if there are at least 2 fetal movements in 20 minutes with acceleration of FHR by 15 beats/min for atleast 15 seconds • Non-reactive: absence of any fetal reactivity. It is associated with poor fetal and neontatal outcome, but there is high incidence of false positive results also. This may be due to fetal sleep, sedative or narcotic drugs, congenital anomalies and premature fetus 37. 37. Procedure :- 38. 38. • Advantages: - • It is a non-invasive test. • The test is simple, inexpensive and takes less time. • There are no contradictions or complications • No special expertise required • Provide immediate answer. • It can be repeated as many times as required without any risk. 39. 39. CONTRACTION STRESS TEST • Tests will be carried out to analyze the baby's well being • CST is based on the observation that during contractions, blood flow to the placenta lessens temporarily. An evaluation is done on how the fetus handles this stress. • Normally fetal heart rate is not affected by contractions 40. 40. • In actual labor after contraction begins, if the fetal heartbeat slows down, it indicates that the fetal is not able to tolerate the decreased blood flow resulting from the contraction. • These decreases are called late decelerations. • If the placenta is not working to capacity or the baby has some problem, Contraction can decrease the oxygen flow and cause the heart rate to drop. 41. 41. • Performing time: after 30 weeks gestation • Position:- • Semi recumbent position • Lateral position 42. 42. Indication: • It is usually conducted if the pregnant woman has had problematic pregnancies in the past or has medical problems in her current pregnancy. • CST is usually performed if Non-stress test showed no change in fetal heart rate when the fetus moved. • To check baby will remain healthy during the reduced oxygen levels that normally occur during contraction 43. 43. Procedure Two fetal monitors will be strapped to the woman's abdomen to record fetal heart rate. • One monitor will pick up uterine contractions and the other picks up fetal heart beat. . Both will readings will record on graph paper. • Stimulate contraction by either nipple stimulation or oxytocin. • Assess the maternal B.P every 10 to 15 min during the test. 44. 44. •The heartbeat will form a line at the top and the maternal contractions will form wavelike lines at the bottom. Both lines will be matched to determine the significance of any decelerations 45. 45. Result/ Interpretation • Negative- no late decelerations are present in the presence of adequate contractions, the placenta is functioning properly and the fetus is doing well. It is the desired result • Positive: late decelerations are present in the presence of adequate contractions. Delivery of baby follows a positive result either by induction of labour or LSCS 46. 46. Amniotic fluid index • Amniotic fluid index (AFI) is a rough estimate of the amount of amniotic fluid and is an index for the fetal well-being. • AFI is the score (expressed in cm) given to the amount of amniotic fluid seen on pregnant uterus and calculated by a ultrasonograph ( ultrasound). 47. 47. • To determine the AFI, doctors may use a four-quadrant technique , when the deepest, unobstructed, vertical length of each pocket of fluid is measured in each quadrant and then added up to the others , or the so called "Single Deepest Pocket" technique 48. 48. INVASIVE METHODS • MATERNAL ALPHA-FETOPROTEIN • AMNIOCENTESIS • CHORIONIC VILLUS SAMPLING (CVS) • CORDOCENTHESIS OR PERCUTANEOUS UMBLICAL CORD BLOOD SAMPLING (PUBS) • FETOSCOPY • AMNIOSCOPY 49. 49. Maternal alpha-fetoprotein screening (MAFP) • A blood test that measures the level of alpha- fetoprotein in the mothers' blood during pregnancy. • AFP is a fetal protein normally produced by the fetal liver and is present in the fluid surrounding the fetus (amniotic fluid), and crosses the placenta into the mother's blood. • The AFP blood test is also called MSAFP (maternal serum AFP 50. 50. Abnormal levels of AFP may signal the following MSAFP level high indicates:- Open neural tube defects (ONTD) such as spina bifida • Other chromosomal abnormalities lead to IUFD • Defects in the abdominal wall of the fetus • Twins more than one fetus is making the protein • A miscalculated due date • Renal anomalies. MSAFP level low indicates • Down’s syndrome • Gestational trophoblastic disease 51. 51. INDICATION • All pregnant women are usually offered the AFP test. But, the doctor may recommend the test, especially if : • Mother is 35 or older • Have a family history of birth defects • Have diabetes • Have taken certain drugs or medication during pregnancy 52. 52. • Time of performing test:- 15-18 weeks • PROCEDURE: 53. 53. Amniocentesis:- • It is a medical procedure used in prenatal diagnosis of chromosomal abnormalities and fetal infections. • In which a small amount of amniotic fluid, which contains fetal tissues, is extracted from the amniotic sac surrounding a developing fetus , and the fetal DNA is examined for genetic abnormalities. 54. 54. • Definition:-it is deliberate puncture of the fluid sac per abdomen. • Indication :- DIAGNOSTIC THERAPUETIC EARLY LATER 55. 55. • Time of performing:- performed between the 15th-20th weeks of pregnancy. Mostly during the 18th week. 56. 56. Nursing responsibility before procedure • Before procedure, take written consent. • Explain the purpose of procedure • Emptying the bladder AND Provide privacy. • Provide supine position with elevated head • The abdominal wall is prepared aseptically and draped. • Check the vital sign and FHR to obtain base line data. • Check USG. • Prophylactic administration of 100 mg of anti –D immunoglobulin in Rh negative mother. • The proposed site of puncture is unfiltered with 2 ml of 1% lignocainE 57. 57. Procedure 58. 58. • Nursing responsibility after procedure: • Fetus should be monitored for short period after procedure, check FHR every 30 minutes. • Tell patient, to report physician if uterine cramping, vaginal bleeding or leakage of fluid or fever. • Strenuous activities should be avoided for 24 hours following an amniocentesis 59. 59. Contraindication:- • Acute skin infections near the site of needle placement. • Maternal fever • Allergies to material used like skin preparation materials, local anesthesia. • May be difficulty in-patient with multiple pregnancies 60. 60. COMPLICATION Maternal complication • Infection • Alloimmunisation of the mother • Preterm labor and delivery • Hemorrhage Fetal complication • Miscarriage • Respiratory distress, • Postural deformities, • Fetal trauma. • Oligohydramnions due to leakage of Amniotic fluid 61. 61. Chorionic villus sampling CVS • Chorionic villous sampling a form of prenatal diagnosis to determine chromosomal or genetic disorders in the fetus . • It entails getting a sample of the chorionic villus (placental tissue) and testing it. • It can be performed in a transvaginally or transabdominal manner 62. 62. Chorionic villus sampling CVS 63. 63. • Performing time: before 15 weeks, usually performed between the 10th and 12th weeks of pregnancy. • Indications:- • Abnormal first trimester screen results • Increased AFP or other abnormal ultrasound findings • Family history of a chromosomal abnormality or other genetic disorder • Parents are known carriers for a genetic disorder • maternal age above 35 64. 64. Procedure • TRANSVAGINALLY: 65. 65. TRANSABDOMINALLY 66. 66. • Contraindication :- • Active vaginal bleeding • Infection • Multiple gestation • HIV infection 67. 67. • Nursing responsibility after procedure:- • Fetus should be monitored for short period after procedure, check FHR every 30 minutes. • Tell patient, to report physician if uterine cramping, vaginal bleeding or leakage of fluid or fever. • Strenuous activities should be avoided for 24 hours following a CVS. • Anti –D immunoglobulin 50 ug IM should be administered following the procedures to the Rh negative women’s 68. 68. • Complications :- • Miscarriage in CVS in about 0.5 - 1%. • Infection and amniotic fluid leakage. The resulting amniotic fluid leak can develop into a condition known as oligohydramnions • Mild risk of Limb Reduction Defects associated with CVS, especially if the procedure is carried out in earlier terms (before 12th week of pregnancy). • Fetal loss. • Infection • Vaginal bleeding 69. 69. Cordocenthesis OR Percutaneous umbilical cord blood sampling (PUBS) • It is a diagnostic genetic test that examines blood from the fetal umbilical cord to detect fetal abnormalities. • PUBS provides a means of rapid chromosome analysis and is useful when information cannot be obtained through amniocentesis, CVS, or ultrasound • Time of performance:-18 weeks of gestation 70. 70. Procedure • PUBS is similar to amniocentesis, but instead of sampling the amniotic fluid which surrounds the fetus, PUBS examines fetal blood 71. 71. • Before the start of the procedure, a local anesthetic is given to the mother. • After the local is in effect, a 25 gauze spinal needle 13 cm in length is usually inserted through the mother's abdominal wall, • An advanced imaging ultrasound determines the location for needle insertion, and the needle is guided through the mother's abdomen and uterine wall into the fetal vein of the umbilical cord, approximately 1-2 cm from the placenta. • The sample can then be sent for chromosomal analysis. 72. 72. COMPLICATIONS • Miscarriage is the primary risk associated with PUBS • Blood loss at the puncture site, • Infection, and • Premature rupture of membranes. • During the procedure, the mother may feel discomfort similar to a menstrual cramp. • Cord hematoma formation • Preterm labor 73. 73. FETOSCOPY • A fibreoptic instrument that can be passed through the abdomen of a pregnant woman to enable examination of the fetus and withdrawal of blood for sampling in prenatal diagnosis. • DEFINITION • Examination of the pregnant uterus by means of a fiber-optic tube. • Time of performing:-18th week of pregnancy 74. 74. • Complication :- • Miscarriage, as high as 12%. • Excessive bleeding, infection, or excessive leakage of the amniotic fluid. • Preterm rupture of the membranes which may require early delivery of your baby . • Mixing your blood with babys blood 75. 75. AMNIOSCOPY • Definition • Direct observation of the foetus and the colour and amount of the amniotic fluid by means of a specially designed endoscope inserted through the uterine cervix. • Contraindicated:- • Cervix is in insufficiently dilated • Complication:- • Sepsis • Rupture of membrane