PROFESSIONAL MIDWIVES SUPPORT FOR NATURAL BIRTH
Who is a Midwife?
A midwife is a professional and trusted expert in natural birth. She looks after pregnant women who have no medical complications. She is a person who has successfully completed a midwifery education programme that is recognised in the country where it is located and that is based on the International Confederation of Midwives (ICM) Essential Competencies for Basic Midwifery Practice and the framework of the ICM Global Standards for Midwifery Education.
A midwife is recognised as a responsible and accountable professional, who works in partnership with women to give the necessary support, care and advice during pregnancy, labour and the postpartum period.
A midwife helps with the immediate care of the newborn and helps mothers breastfeed as well. She is highly skilled, competent and confident of recognising complications, offers immediate emergency treatment and refer on time to a higher centre. This helps reduce maternal deaths and long-term morbidity.
The uniqueness of Midwifery
A professional midwife is not a doctor. She is not a nurse. She is a unique professional trained to be with the woman, to offer midwifery care and support through her labour and the birth of her baby. The continuous support of a professional midwife helps provide the environment of trust.
The woman's fears are reduced, her physical, emotional and psychological needs are met within an atmosphere of respectful care.
What to expect from a Midwife during labour?
Gentle, nurturing care which will respect you and your beliefs.
Respect for your birth preferences and honest communication, should there be a need to seek other options.
Encouragement to move around and to adopt any position you wish to, in the active phase of labour.
Support the position of choice for birth - squatting, knee-chest, lateral (lying on the side), upright, standing.
Freedom to eat and drink. You will be given a menu with safe options.
The midwife will help you breastfeed your baby and will leave your side only after you are confident and comfortable.
Why should women be given the choice?
Midwifery care is as safe as an obstetrician- assisted delivery, for women with uncomplicated pregnancies. Studies have also shown other benefits of availing midwifery services, such as: increased maternal satisfaction, shorter labour, lower need for pain relief, higher rates of normal births and lower need for Caesarean Section.
Natural birth
Childbirth is a natural, physiological function and women are biologically programmed to deliver normally. Our personalised midwifery support will make your pregnancy a joyful and memorable event, free from all unnecessary medical interventions.
We at Arokya believe respectful birthing is a human right, and every woman must be offered professional Midwifery care.
Professional Midwives Support For Natural Birth
First Trimester Fetal Health
Fetal health check
Pregnancy is a wonderful time filled with excitement and anticipation of the addition of a new member in the family. The early weeks of pregnancy can be an anxious time. Like most expectant mothers, you seek reassurance that your baby will be in your arms after a smooth pregnancy. The vast majority of the babies are normal. However, there may be a serious health problems affecting 2-3% of babies. You may wish to find out early in your pregnancy, if your baby is at increased risk of a serious health condition.
Prenatal screening
Prenatal screening tests can help identify the mother at high risk of these problems. Screening has to be done ideally in the First Trimester of pregnancy i.e., 11-13+6 weeks. The screening tests are either an ultrasound scan or a blood test or a combination of both.
First trimester screening
This health check requires your medical history, blood pressure measurement, ultrasound examination and a blood test.
CONDITIONS TO BE SCREENED
Birth defects or congenital malformations are problems that happen while a baby is developing in the mother's womb. Most birth defects happen during the first three months of pregnancy. A birth defect may affect how the baby looks or behaves or both. Birth defects can range from mild to severe. For most birth defects, the cause is unknown. However, birth defects may occur due to genetics, chromosomes, exposure to medicines etc.
Neural tube defects are birth defects that involve the central nervous system. This system includes the brain and the spinal cord. It is formed from a structure in the developing embryo called the neural tube. As the embryo develops in the mother, the neural tube closes completely.
However, if all or part of the tube fails to close, leaving an opening, the baby has a neural tube defect. Neural tube defect is one of the most common birth defects in India.
The first-trimester scan helps to identify up to 50% of major birth defects. Along with a blood test, the detection rate of Spina Bifida increases up to 95-99%.
COMMON CHROMOSOMAL ABNORMALITIES
All of us have 23 pairs of chromosomes. Each chromosome has 2 copies. Chromosomal abnormality occurs in either the number or structure of a chromosome. Intellectual and physical development is affected as a result of alteration in the chromosomes.
All expectant mothers are at risk of having a baby with a chromosomal abnormality. Trisomy 21, 18, and Trisomy 13 are common chromosomal abnormalities.
DOWN SYNDROME (TRISOMY 21)
Down Syndrome is the most commonly occurring chromosomal abnormality. It is caused by the presence of an extra copy of chromosome number 21 in the cells of the developing baby.
The incidence of Down Syndrome is about 1 in 700 live births. Down Syndrome is the most common cause of severe learning disability in children and is often associated with physical problems such as heart defects (40%) or difficulties with sight and hearing. It may also be associated with childhood leukemia.
TRISOMY 18 AND TRISOMY 13
Trisomy 18 and Trisomy 13 are comparatively rare and severe forms of chromosomal abnormality. These are associated with severe mental and physical disabilities and also life-threatening complications in the baby's first months and years.
Scan alone can predict up to 60-70% of chromosomal abnormalities. However, Scan and Blood Test together can predict up to 90%.
The first trimester screening test is performed to know whether your risk of having a baby with chromosomal abnormalities is increased or decreased. With expert counselling, you will then be able to decide if you need a further diagnostic test. The diagnostic test gives definite information about the presence of chromosomal abnormalities.
PREECLAMPSIA
It is a condition a woman can develop during pregnancy (at any time after 20 weeks of pregnancy) or up to six weeks after birth. This complication of pregnancy is marked by high blood pressure and protein in the urine. Left untreated, the mother and her baby are at increased risk of serious health complications, including growth restriction and prematurity. Early detection offers the opportunity to identify and treat women who are at risk.
This health check requires an ultrasound examination, blood pressure measurement and a blood test.
The chance of developing Preeclampsia can be estimated by ultrasound scan alone up to 60%, whereas a scan and a blood test together can assess the risk up to 90%.
How is the First Trimester Fetal Health check done?
First Trimester Fetal Health Check includes four components:
Maternal and Family History
Blood Pressure Measurement
Ultrasound Scan
Blood Test (eFTS)
After your registration at the Department of Fetal Medicine, you will be taken to the prenatal screening room. Your doctor/nurse will ask you some questions (medical history) about your and your family's health. Your doctor will also check your height, weight and blood pressure. Afterwards, you will undergo a detailed ultrasound scan.
Depending upon your baby's position and some technical issues, the scan may take approximately an hour. If your baby is not in a position, you may be asked to wait for a while or may be asked to come back for the next session.
As soon as your scan is over, you will be guided to the clinical laboratory for a blood test.
eFTS: enhanced First Trimester Screening includes a simple blood test
Finally, in the laboratory a blood sample will be taken between 11 to 13+6 weeks, to look at some biochemical markers in your blood, which will help us complete the assessment. This blood test is called eFTS.
The laboratory will measure the relative concentrations of the biochemical markers present in an expectant mother's body (PAPP-A, free hCGB, PIGF and AFP). Any deviation from the normal range is indicative of some irregularity and may need further investigations.
LATE BOOKING
What is the alternative test, if I miss the First Trimester Screening?
Second Trimester Screening: Ultrasound scan and blood test
If you have missed the opportunity of First Trimester screening, you can opt for the Second Trimester screening which also involves scan and blood test (Quadruple test). However, the risk estimation for Down Syndrome is lower than that of the first trimester (80% vs 95%).
Non-invasive Prenatal Test
WHAT IS NON-INVASIVE PRENATAL TEST (NIPT)?
It is a blood test which determines the presence of free fetal DNA in maternal blood. This fetal DNA, when analysed, gives us an estimate of the risk of the baby having Down Syndrome. The NIPT is sensitive up to 95% for Trisomy 21, 18 and Trisomy 13. If fetal DNA testing is positive for Down Syndrome, then you will have to undergo further confirmatory tests.
What do the results of the Prenatal Screening mean?
It must be clearly understood that the results represent risks and not diagnostic outcomes.
A low-risk result implies that no further test for Down Syndrome are required. These mothers can be followed with serial ultrasound scans.
A high-risk result requires further diagnostic tests. You will be guided by the Fetal Medicine experts.
For most women, the checks will assure that mother and baby are doing well and no further action is required. For a small group of women, there will be an early warning signal that indicates that the Doctor may need to request further tests or prescribe some medication for the remainder of the pregnancy to support mother and baby. By doing an assessment early in pregnancy, it enables a care pathway to be determined for you and your baby towards a happy outcome.
JUST REMEMBER!
Most babies are born healthy. Early and optimal screening ensures a happy and peaceful pregnancy.