DEVELOPMENT
of the
HUMAN EMBRYO
and
FETUS:  VIABILITY,
 

 Virgin and Child, Master of Moulins, 1499


1. EMBRYONIC DEVELOPMENT;   2. FETAL DEVELOPMENT  3. VIABILITY;    4. ABORTION PILL


PLEASE note that the black-and-white photographs shown here were assembled by the Carnegie Embryology Institute over several decades, beginning in 1914, as part of a national effort to identify, describe, and standardize the stages of  human embryological and fetal development.  The photographs are of embryos that were the result of spontaneous miscarriages or that were discovered during a necessary hysterectomy.  In other words, these are not photographs of intentionally-aborted embryos.

For embryo sizes compared with a US penny:
http://virtualhumanembryo.lsuhsc.edu/HEIRLOOM/Stages/Stages_intro.html


 

 

 

 

WEEK 3

 

 

 

 

 

   

 

STAGE 11;
23 - 26 Days;
2.5 - 4.5 mm;; Somite Number 13 - 20;
rostral neuropore closes; Carnegie Stage 11; Features: rostral neuropore closing, forebrain, neural tube in region of developing spinal cord, somites, caudal neuropore, connecting stalk, amnion

 

   

 

 

 

 

WEEK 4

 

 

 

 

 

   

 

STAGE 12;
26 - 30 Days;
3 - 5 mm;; Somite Number 21 - 29;
caudal neuropore closes; Features: day 26, 27 somites, forebrain, site of lens placode, site of otic placode , stomodeum, 1st pharyngeal arch, 2nd pharyngeal arch, 3rdpharyngeal arch, heart prominence, somite

 

   

 

 

 

 

WEEK 5

 

 

 

 

 

   

 

STAGE 13;
28 - 32 Days; (week 5);
4 - 6 mm;; Somite Number 30;
leg buds, lens placode, pharyngeal arches; Features: site of midbrain, lens placode, site of nasal placode, 1,2,3 pharyngeal arches, L. ventricular prominence of heart, L. atrial prominence of heart, umbilical cord, lower limb bud, mesonephric prominence, upper limb bud;

 

 

STAGE 14;
31 - 35 Days;
5 - 7 mm;;
lens pit, optic cup; Day 32 Features: midbrain, nasal placode, lens pit, 1,2,3 pharyngeal arches, fourth ventricle of brain, 1st pharyngeal groove, heart prominence, cervical sinus, upper limb bud, mesonephric ridge, lower limb bud, umbilical cord

 

 

STAGE 15;
35 - 38 Days;
7 - 9 mm;; lens vesicle, nasal pit, hand plate

 

   

 

 

 

 

WEEK 6

 

 

 

 

 

   

 

STAGE 16;
37 - 42 Days; (week 6);
8 - 11 mm;
nasal pits moved ventrally, auricular hillocks, foot plate; (day 40); Features: eye showing retinal pigment, nasolacrimal groove, nasal pit, fourth ventricle of brain, umbilical cord, 1st and 2nd pharyngeal arches, cervical sinus, heart, developing arm with hand plate, foot plate

 

 

STAGE 17;
42 - 44 Days;
11 - 14 mm;; f
inger rays; day 42); Features: pigmented eye, nasal pit, nasolacrimal groove, external acoustic meatus, auricular hillock, heart, digital rays, liver pronminance, thigh, ankle, foot plate, umbilical cord

 

   

 

 

 

 

WEEK 7

 

 

 

 

 

   

 

STAGE 18;
44 - 48 Days;
(WEEK 7);
13 - 17 mm;; ossification commences

 

 

STAGE 19;
48 - 51 Days;
16 - 18 mm;;
straightening of trunk; day 48) Features: eyelid, eye, external acoustic meatus, auricle of external ear, digital ray, wrist, liver prominence

 

 

STAGE 20;
51 - 53 Days;
(week 8);
18 - 22 mm;
upper limbs longer and bent at elbow day 51); Features: scalp vascular plexus, eylid, eye, nose, external acoustic meatus, auricle of external ear, arm, elbow, wrist, liver prominence, digital rays

 

 

STAGE 21;
53 - 54 Days;
22 - 24 mm;
hands and feet turned inward; day 52); Features: scalp vascular plexus, eylid, eye, nose, auricle of external ear, arm, elbow, wrist, knee, notch between digital rays, umbilical cord;

 

   

 

 

 

 

WEEK 8

 

 

 

 

 

   

 

STAGE 22;
54 - 56 Days;
23 - 28 mm;;
eyelids, external ears

 

 

STAGE 23;
56 - 60 Days;
27 - 31 mm;; rounded head, body and limbs; Features: scalp vascular plexus, eylid, eye, nose, auricle of external ear, mouth, sholder, arm, elbow, wrist, toes separated, sole of foot, umbilical cord

 

   

 

 

 

 


FETAL DEVELOPMENT

 

 

 

The end of the eighth week marks the END of the “EMBRYONIC PERIOD” and the BEGINNING of the “FETAL PERIOD”.

 

 

 


 

 

 

WEEKS 9-12

 

 

 

 

 

WEEKS 13-16

 

 

 

 

 

WEEK 20

 

 


VIABILITY


 

 

STATISTICS on VIABILITY
from Ford, The Prenatal Person, ch. 9, "Newborns"

 

 


Table 9.3: Neonatal intensive care unit, Loyola University Medical Center, survival rates, 1990—4

Gestational age, weeks

Survivors %

22—3

19 %

24—5

63 %

26—7

88 %

Source: modified from “Neonatal Survival Rates”  in Cambridge Quarterly of Healthcare Ethics 8 (1999):162.


Table 9.4: Survival rates by gestational age, 1994–6

Gestational age, weeks

Survivors percentage

Live births

23

35.5 %

31

24

65.6 %

36

25

73.9 %

46

26

85.9 %

64

28

96.0 %

75

32

98.1 %

262

Source: modified and calculated from data in the Royal Women’s Hospital in Melbourne,  Medical Journal of Australia, June 7, 1999.

 

 

 


 

 

WEEK 24

 

 

 

 

WEEKS 25-28

 

 

 

 

 

 

 

WEEKS 29-32

 

 

 

 

WEEK 36

 

 

 

 

WEEKS 37-40

 

 

 

 

 

 

 

 

 

 


ABORTION PILL


THE “ABORTION PILL”
 



In 2016 the U.S. Food and Drug Administration approved a two-drug combination of Mifeprex (also called RU-486 or mifepristone) and Cytotec (commonly known as misoprostol) to induce abortion without surgery. In 2019 the Centers for Disease Control and Prevention reported that approximately 42 percent of all abortions in the U.S. were medication-based.

To start the process, a person takes mifepristone within 10 weeks from their last period. One or two days later they take misoprostol. Both drugs work individually, but they are more effective together. Mifepristone blocks progesterone's action on the uterus, making it incapable of supporting a pregnancy. Misoprostol, among other things, starts uterine contractions.
 

 



MIFEPRISTONE (RU-486) EFFECT
 


 




MISOPROSTOL  EFFECT
 





 

 

 

from the PLANNED PARENTHOOD WEBSITE
https://www.plannedparenthood.org/learn/abortion/the-abortion-pill

 

How does the abortion pill work?

“Abortion pill” is the common name for using two different medicines to end a pregnancy: mifepristone and misoprostol.

First, you take a pill called mifepristone. Pregnancy needs a hormone called progesterone to grow normally. Mifepristone blocks your body’s own progesterone, stopping the pregnancy from growing.

Then you take the second medicine, misoprostol, either right away or up to 48 hours later. This medicine causes cramping and bleeding to empty your uterus. It’s kind of like having a really heavy, crampy period, and the process is very similar to an early miscarriage. If you don’t have any bleeding within 24 hours after taking the second medicine, call your nurse or doctor.

Your doctor or nurse will give you both medicines at the health center. When and where you’ll take them depends on state laws and your health center's policies. Your doctor or nurse will give you detailed directions about where, when, and how to take the medicines. You may also get some antibiotics to prevent infection.

How effective is the abortion pill?

The abortion pill is very effective. The effectiveness depends on how far along you are in your pregnancy when you take the medicine



The abortion pill usually works, but if it doesn’t, you can take more medicine or have an in-clinic abortion to complete the abortion.

When can I take the abortion pill?

Depending on where you live, you may be able to get a medication abortion up to 77 days (11 weeks) after the first day of your last period. If it has been 78 days or more since the first day of your last period, you can have an in-clinic abortion to end your pregnancy.

 

 

 

DRUGS USED in POST-SEX CONTRACEPTION


 

  DRUGS USED in POST-SEX CONTRACEPTION
The Morning-After Pill

 



LEVONORGESTREL
(Plan B)

ULIPRISTAL
(Ella)

Progestogen (progesterone-like drug)with weak androgenic activity.

  A selective progesterone receptor modulator (SPRM): acts on the progesterone receptor causing different effects in different tissues.

Both drugs work by blocking or delaying ovulation
and by delaying maturation of the uterine endometrium (lining)


 

LEVONORGESTREL (Plan B)

Levonorgestrel is a progestogen with weak androgenic activity. It has no other important hormonal activity

 

ULIPRISTAL (Ella)

As an SPRM*, ulipristal acetate has partial agonistic as well as antagonistic effects on the progesterone receptor. Ulipristal acetate exhibits similar potency to antagonize progesterone receptor as mifepristone in vitro. Works by blocking or delaying ovulation and of delaying the maturation of the endometrium

*A selective progesterone receptor modulator (SPRM) is an agent that acts on the progesterone receptor (PR), the biological target of progestogens like progesterone. their action differs in different tissues, i.e. agonist in some tissues while antagonist in others. This mixed profile of action leads to stimulation or inhibition in tissue-specific manner

 


 

  DRUGS USED to INDUCE ABORTION
The Morning-After Pill

 



 

 

MIFEPRISTONE
(RU-486)

MISOPROSTOL

Antiprogestogen: progesterone-receptor blocker, causes death and detachment of placenta.

 Prostaglandin: induces uterine contractions


METHOTREXATE
 

An antimetabolite: a drug that interfere with one or more enzymes or their reactions that are necessary for DNA synthesis. Originally used in cancer treatment because it destroys rapidly-dividing cells. As an abortifacient it destroys trophoblast cells: i.e. tissue that later becomes the placenta.

 


DRUGS USED to INDUCE ABORTION

MIFEPRISTONE
(antiprogestogen progesterone-receptor blocker, causes death and detachment of placenta)

 

A progesterone-blocker, when used to induce abortion the drug causes decidual necrosis (death of placental and chorionic tissue)*, leading to detachment of the placenta and death of the embryo/fetus

* "The effects of mifepristone on the structure of human decidua and chorion and Bax and Bcl-2 expression at early stage of pregnancy." Fei Tian, Hua Han, et.al. BMC Pharmacology and Toxicology vol. 23, Art.: 55 (July 23, 2022)https://bmcpharmacoltoxicol.biomedcentral.com/articles/10.1186/s40360-022-00592-4

Mifepristone is a steroidal antiprogestogen (IC50 = 0.025 nM for the PR), as well as an antiglucocorticoid (IC50 = 2.2 nM for the GR) and antiandrogen (IC50 = 10 nM for the AR) to a much lesser extent. It antagonizes cortisol action competitively at the receptor level.

In the presence of progesterone, mifepristone acts as a competitive progesterone receptor antagonist (in the absence of progesterone, mifepristone acts as a partial agonist).

 

MISOPROSTOL
(prostaglandin – induces uterine contractions)

Misoprostol, a prostaglandin analog, binds to myometrial cells to cause strong myometrial contractions leading to expulsion of embryonic/fetal tissue. This agent also causes cervical ripening with softening and dilation of the cervix.

 

METHOTREXATE
Antimetabolite - destroys placental and embryonic/fetal tissue)

An antimetabolite: a drug that interfere with one or more enzymes or their reactions that are necessary for DNA synthesis. Used in cancer treatment because it destroys rapidly-dividing cells. As an abortifacient it destroys trophoblast cells: i.e. tissue that later becomes the placenta.  Since the cells of the embryo/fetus are also rapidly-dividing, it is hard to imagine that methotrexate does not directly kill embryonic/fetal cells, as well..

Destroys trophoblast ( https://pubmed.ncbi.nlm.nih.gov/22510625/  ) Methotrexate: the pharmacology behind medical treatment for ectopic pregnancyCatherine S Stika, Clin Obstet Gynecol,2012 Jun;55(2):433-9.

From the Mayo Clinic page on medical abortion

https://www.mayoclinic.org/tests-procedures/medical-abortion/about/pac-20394687

Medical abortion can be done using these medicines:

there are many states that have very few abortion providers, meaning that abortion is not effectively available to people without means to travel. For example, in Mississippi 99% of parishes (counties) do not have an abortion provider. Other states in which more than 95% of counties do not have abortion providers include Nebraska, the Dakotas, Kansas, West Virginia, Wisconsin and Wyoming.

 


This Webpage was created for a workshop held at Saint Andrew's Abbey, Valyermo, California in 2003....x....   “”.