PSY FPX 6010 Assessment 1

Assessment Overview

PSY FPX 6010 Assessment 1: Noninvasive Antenatal Testing (NIPT) is an inheritable webbing system used during gestation to describe chromosomal abnormalities similar to trisomy 21 (Down pattern), trisomy 18, and trisomy 13. Conducted via a simple motherly blood test, NIPT analyzes cell-free fetal DNA with high delicacy and minimum threat. Though not individual, it provides precious perceptivity for early gestation care and informed decision-making. 

What’s Included:

Sample Assessment Paper

General Information

Fetal health is of the highest importance when one is pregnant, and it involves assessing genetic and chromosomal factors. Various tests, invasive and noninvasive, are employed to detect such risks during pregnancy (Gross, 2019). Noninvasive prenatal testing (NIPT) has been increasingly popular since 2011 to assess genetic abnormalities without risking the fetus’s life (Montgomery & Thayer, 2020). NIPT does not make any diagnosis but identifies heightened risks (Montgomery & Thayer, 2020).

Description of NIPT

NIPT scans cell-free DNA from the pregnant woman’s bloodstream with little danger, like a standard blood test (Montgomery & Thayer, 2020). NIPT detects common flaws like trisomy 21, 18, and 13 with a high degree of accuracy (Samura, 2020). NIPT can also detect the sex of the fetus and usually is performed around the tenth week of pregnancy (Montgomery & Thayer, 2020).

Benefits and Limitations

NIPT provides psychological advantages, minimizing stress on expectant parents (Kater-Kuipers et al., 2018). False reassurance is, however, a possibility given its imperfect nature, and false positives or negatives can result (Samura, 2019). Nevertheless, NIPT provides parents with time to prepare for the child’s possible medical requirements and enables closer surveillance during pregnancy (Montgomery & Thayer, 2020).

The Genetic Counselor

Genetic counseling is relevant to informing expectant parents about the implications of NIPT results (Kater-Kuipers et al., 2021). It helps manage complex decisions and provides assistance, such as referral to advocacy groups (Kater-Kuipers et al., 2021).

Conclusion

NIPT is safe and reliable for assessing fetal health, particularly in complex pregnancies. However, its use necessitates informed decision-making, which may be enhanced using genetic counseling.

PSY FPX 6010 Assessment 1 Noninvasive Prenatal Testing Overview 

Kater-Kuipers, A., Bunnik, E. M., de Beaufort, I. D., & Galjaard, R. (2018). Limits to the scope of non-invasive prenatal testing (NIPT): an analysis of the international ethical framework for prenatal screening and an interview study with Dutch professionals. BMC Pregnancy and Childbirth, 18(1), 409. https://doi.org/10.1186/s12884-018-2050-4

Labonté, V., Alsaid, D., Lang, B., & Meerpohl, J. J. (2019). Psychological and social consequences of non-invasive prenatal testing (NIPT): a scoping review. BMC Pregnancy and Childbirth, 19(1), 385. doi: https://doi.org/10.1186/s12884-019-2518-x

Montgomery, S., & Thayer, Z. M. (2020). The influence of experiential knowledge and societal perceptions on decision-making regarding non-invasive prenatal testing (NIPT). BMC Pregnancy and Childbirth, 20, 1-14. DOI: http://dx.doi.org/10.1186/s12884-020-03203-4

PSY FPX 6010 Assessment 1 Noninvasive Prenatal Testing Overview 

Samura, O. (2020). Update on noninvasive prenatal testing: A review based on current worldwide research. The Journal of Obstetrics and Gynaecology Research, 46(8), 1246–1254. DOI: https://doi.org/10.1111/jog.14268

References

  • Azri, S., Larmar, S., & Cartmel, J. (2014). Social work’s role in prenatal diagnosis and genetic services: Current practice and future potential. Australian Social Work, 67(3), 348–362. https://doi.org/10.1186/s12884-018-2050-4
  • Benoy, M.E., Iruretagoyena, J.I., Birkeland, L.E., & Petty, E.M. (2021). The impact of insurance on equitable access to non-invasive prenatal screening (NIPT): private insurance may not pay. Journal of Community Genetics, 12(1), 185-197 http://dx.doi.org/10.1038/s41431-020-0686-9
  • Gross, D. (2019). Infancy: Development from birth to age 3 (3rd ed.). Rowman & Littlefield.
  • Kater-Kuipers A., Bakkeren, I. M., Riedijk, S. R., Go Attie, T. J. I., Polak, M. G., Galjaard, R. H., Bunnik, E. M. (2021). Non-invasive prenatal testing (NIPT): Societal pressure or freedom of choice? A vignette study of Dutch citizens’ attitudes. European Journal of Human Genetics: EJHG, 29(1), 2-10. DOI: http://dx.doi.org/10.1038/s41431-020-0686-9

Step-by-Step Guide

  1. Consultation for NIPT with a healthcare provider or inheritable counselor. 
  2. Blood Sample Collection A small blood sample is drawn from the pregnant existent (around 10 weeks). 
  3. Laboratory Analysis The lab examines cell-free DNA for chromosomal abnormalities. 
  4. Result Interpretation: Results indicate the liability of inheritable conditions (not a verified opinion). 
  5. Follow-Up Counseling Genetic counselors explain results, bandy emotional and medical options, and recommend further testing if demanded. 

Frequently Asked Questions (FAQs)

Integrity Note

Use this example for learning and structure only. Do not submit as your own work.
We are an independent resource and are not affiliated with any university.

Essay-Writing-Service-For-Students-Best-Essay-Writer-Online.png

“I paid the service to write my research paper.” They wrote an excellent paper with a lot of research and correct citations. “Great excellent work!”

Order ID # 00889

BSN - Capella University

Jonathan Nicole

⭐⭐⭐⭐⭐

Experience : 10+ Years in Nursing.
Specialization : BSN, MSN

Jessica Walker

⭐⭐⭐⭐⭐

Experience : 10+ Years in Nursing.
Specialization : MSN, DNP

Denis Peterson

⭐⭐⭐⭐⭐

Experience : 10+ Years in Nursing.
Specialization : DNP, PSY

How it Works

We provide services to registered nurses who are taking classes toward their BSN or MSN degrees.

You cannot copy content of this page

Nursing Papers Help even with a 3-hour deadline!

Get Any Assessment For Free

Verification is required to avoid bots.