In placental mammals, the umbilical cord (also called the navel string, birth cord or funiculus umbilicalis) is a conduit between the developing embryo or fetus and the placenta. During prenatal development, the umbilical cord is physiologically and genetically part of the fetus and (in humans) normally contains two arteries (the umbilical arteries) and one vein (the umbilical vein), buried within Wharton's jelly. The umbilical vein supplies the fetus with oxygenated, nutrient-rich blood from the placenta. Conversely, the fetal heart pumps low oxygen, nutrient-depleted blood through the umbilical arteries back to the placenta.
Structure and developmentEdit
The umbilical cord develops from and contains remnants of the yolk sac and allantois. It forms by the fifth week of development, replacing the yolk sac as the source of nutrients for the embryo. The cord is not directly connected to the mother's circulatory system, but instead joins the placenta, which transfers materials to and from the maternal blood without allowing direct mixing. The length of the umbilical cord is approximately equal to the crown-rump length of the fetus throughout pregnancy. The umbilical cord in a full term neonate is usually about 50 centimeters (20 in) long and about 2 centimeters (0.75 in) in diameter. This diameter decreases rapidly within the placenta. The fully patent umbilical artery has two main layers: an outer layer consisting of circularly arranged smooth muscle cells and an inner layer which shows rather irregularly and loosely arranged cells embedded in abundant ground substance staining metachromatic. The smooth muscle cells of the layer are rather poorly differentiated, contain only a few tiny myofilaments and are thereby unlikely to contribute actively to the process of post-natal closure.
The umbilical cord lining is a good source of mesenchymal and epithelial stem cells. Umbilical cord mesenchymal stem cells (UC-MSC) have been used clinically to treat osteoarthritis, autoimmune diseases, and multiple other conditions. Their advantages include a better harvesting, and multiplication, and immunosuppressive properties that define their potential for use in transplantations. Their use would also overcome the ethical objections raised by the use of embryonic stem cells.
The umbilical cord contains Wharton's jelly, a gelatinous substance made largely from mucopolysaccharides that protects the blood vessels inside. It contains one vein, which carries oxygenated, nutrient-rich blood to the fetus, and two arteries that carry deoxygenated, nutrient-depleted blood away. Occasionally, only two vessels (one vein and one artery) are present in the umbilical cord. This is sometimes related to fetal abnormalities, but it may also occur without accompanying problems.
It is unusual for a vein to carry oxygenated blood and for arteries to carry deoxygenated blood (the only other examples being the pulmonary veins and arteries, connecting the lungs to the heart). However, this naming convention reflects the fact that the umbilical vein carries blood towards the fetus's heart, while the umbilical arteries carry blood away.
The blood flow through the umbilical cord is approximately 35 ml / min at 20 weeks, and 240 ml / min at 40 weeks of gestation. Adapted to the weight of the fetus, this corresponds to 115 ml / min / kg at 20 weeks and 64 ml / min / kg at 40 weeks.
For terms of location, the proximal part of an umbilical cord refers to the segment closest to the embryo or fetus in embryology and fetal medicine, and closest to the placenta in placental pathology, and opposite for the distal part, respectively.
Connection to fetal circulatory systemEdit
The umbilical cord enters the fetus via the abdomen, at the point which (after separation) will become the umbilicus (or navel). Within the fetus, the umbilical vein continues towards the transverse fissure of the liver, where it splits into two. One of these branches joins with the hepatic portal vein (connecting to its left branch), which carries blood into the liver. The second branch (known as the ductus venosus) bypasses the liver and flows into the inferior vena cava, which carries blood towards the heart. The two umbilical arteries branch from the internal iliac arteries and pass on either side of the urinary bladder into the umbilical cord, completing the circuit back to the placenta.
Changes after birthEdit
In absence of external interventions, the umbilical cord occludes physiologically shortly after birth, explained both by a swelling and collapse of Wharton's jelly in response to a reduction in temperature and by vasoconstriction of the blood vessels by smooth muscle contraction. In effect, a natural clamp is created, halting the flow of blood. In air at 18 °C, this physiological clamping will take three minutes or less. In water birth, where the water temperature is close to body temperature, normal pulsation can be 5 minutes and longer.
Closure of the umbilical artery by vasoconstriction consists of multiple constrictions which increase in number and degree with time. There are segments of dilatations with trapped uncoagulated blood between the constrictions before complete occlusion. Both the partial constrictions and the ultimate closure are mainly produced by muscle cells of the outer circular layer. In contrast, the inner layer seems to serve mainly as a plastic tissue which can easily be shifted in an axial direction and then folded into the narrowing lumen to complete the closure. The vasoconstrictive occlusion appears to be mainly mediated by serotonin and thromboxane A2. The artery in cords of preterm infants contracts more to angiotensin II and arachidonic acid and is more sensitive to oxytocin than in term ones. In contrast to the contribution of Wharton's jelly, cooling causes only temporary vasoconstriction.
Within the child, the umbilical vein and ductus venosus close up, and degenerate into fibrous remnants known as the round ligament of the liver and the ligamentum venosum respectively. Part of each umbilical artery closes up (degenerating into what are known as the medial umbilical ligaments), while the remaining sections are retained as part of the circulatory system.
Problems and abnormalitiesEdit
A number of abnormalities can affect the umbilical cord, which can cause problems that affect both mother and child:
- Umbilical cord compression can result from, for example, entanglement of the cord, a knot in the cord, or a nuchal cord, (which is the wrapping of the umbilical cord around the fetal neck) but these conditions do not always cause obstruction of fetal circulation.
- Velamentous cord insertion
- Single umbilical artery
- Umbilical cord prolapse
- Vasa praevia
Clamping and cuttingEdit
The cord can be clamped at different times; however, delaying the clamping of the umbilical cord until at least one minute after birth improves outcomes as long as there is the ability to treat the small risk of jaundice if it occurs. Clamping is followed by cutting of the cord, which is painless due to the absence of nerves. The cord is extremely tough, like thick sinew, and so cutting it requires a suitably sharp instrument. While umbilical severance may be delayed until after the cord has stopped pulsing (1–3 minutes after birth), there is ordinarily no significant loss of either venous or arterial blood while cutting the cord. Current evidence neither supports, nor refutes, delayed cutting of the cord, according to the American Congress of Obstetricians and Gynecologists (ACOG) guidelines.
There are umbilical cord clamps which incorporate a knife. These clamps are safer and faster, allowing one to first apply the cord clamp and then cut the umbilical cord. After the cord is clamped and cut, the newborn wears a plastic clip on the navel area until the compressed region of the cord has dried and sealed sufficiently.
The length of umbilical left attached to the newborn varies by practice; in most hospital settings the length of cord left attached after clamping and cutting is minimal. In the United States, however, where the birth occurred outside of the hospital and an emergency medical technician (EMT) clamps and cuts the cord, a longer segment up to 18 cm (7 in) in length is left attached to the newborn.
The remaining umbilical stub remains for up to 10 days as it dries and then falls off.
Early versus delayed clampingEdit
A Cochrane review in 2013 came to the conclusion that delayed cord clamping (between one and three minutes after birth) is "likely to be beneficial as long as access to treatment for jaundice requiring phototherapy is available". In this review delayed clamping, as contrasted to early, resulted in no difference in risk of severe maternal postpartum hemorrhage or neonatal mortality, and a low Apgar score. On the other hand, delayed clamping resulted in an increased birth weight of on average about 100 g, and an increased hemoglobin concentration of on average 1.5 g/dL with half the risk of being iron deficient at three and six months, but an increased risk of jaundice requiring phototherapy.
In 2012, the American College of Obstetricians and Gynecologists officially endorsed delaying clamping of the umbilical cord for 30–60 seconds with the newborn held below the level of the placenta in all cases of preterm delivery based largely on evidence that it reduces the risk of intraventricular hemorrhage in these children by 50%.[obsolete source] In the same committee statement, ACOG also recognize several other likely benefits for preterm infants, including "improved transitional circulation, better establishment of red blood cell volume, and decreased need for blood transfusion". In January 2017, a revised Committee Opinion extended the recommendation to term infants, citing data that term infants benefit from increased hemoglobin levels in the newborn period and improved iron stores in the first months of life, which may result in improved developmental outcomes. ACOG recognized a small increase in the incidence of jaundice in term infants with delayed cord clamping, and recommended policies be in place to monitor for and treat neonatal jaundice. ACOG also noted that delayed cord clamping is not associated with increased risk of postpartum hemorrhage.
Several studies have shown benefits of delayed cord clamping: A meta-analysis showed that delaying clamping of the umbilical cord in full-term neonates for a minimum of 2 minutes following birth is beneficial to the newborn in giving improved hematocrit, iron status as measured by ferritin concentration and stored iron, as well as a reduction in the risk of anemia (relative risk, 0.53; 95% CI, 0.40–0.70). A decrease was also found in a study from 2008. Although there is higher hemoglobin level at 2 months, this effect did not persist beyond 6 months of age. Not clamping the cord for three minutes following the birth of a baby improved outcomes at four years of age. A delay of three minutes or more in umbilical cord clamping after birth reduce the prevalence of anemia in infants.
Negative effects of delayed cord clamping include an increased risk of polycythemia. Still, this condition appeared to be benign in studies. Infants whose cord clamping occurred later than 60 seconds after birth had a higher rate of neonatal jaundice requiring phototherapy.
Delayed clamping is not recommended as a response to cases where the newborn is not breathing well and needs resuscitation. Rather, the recommendation is instead to immediately clamp and cut the cord and perform cardiopulmonary resuscitation. The umbilical cord pulsating is not a guarantee that the baby is receiving enough oxygen. However, where possible, one should perform cardiopulmonary resuscitation with the cord still attached, to receive both benefits of oxygen from the cord and from the intervention.
Some parents choose to omit cord severance entirely, a practice called "lotus birth" or umbilical nonseverance. The entire intact umbilical cord is allowed to dry and separates on its own (typically on the 3rd day after birth), falling off and leaving a healed umbilicus.
Umbilical cord catheterizationEdit
As the umbilical vein is directly connected to the central circulation, it can be used as a route for placement of a venous catheter for infusion and medication. The umbilical vein catheter is a reliable alternative to percutaneous peripheral or central venous catheters or intraosseous canulas and may be employed in resuscitation or intensive care of the newborn.
From 24 to 34 weeks of gestation, when the fetus is typically viable, blood can be taken from the cord in order to test for abnormalities (particularly for hereditary conditions). This diagnostic genetic test procedure is known as percutaneous umbilical cord blood sampling.
Storage of cord bloodEdit
The blood within the umbilical cord, known as cord blood, is a rich and readily available source of primitive, undifferentiated stem cells (of type CD34-positive and CD38-negative). These cord blood cells can be used for bone marrow transplant.
Some parents choose to have this blood diverted from the baby's umbilical blood transfer through early cord clamping and cutting, to freeze for long-term storage at a cord blood bank should the child ever require the cord blood stem cells (for example, to replace bone marrow destroyed when treating leukemia). This practice is controversial, with critics asserting that early cord blood withdrawal at the time of birth actually increases the likelihood of childhood disease, due to the high volume of blood taken (an average of 108ml) in relation to the baby's total supply (typically 300ml). The Royal College of Obstetricians and Gynaecologists stated in 2006 that "there is still insufficient evidence to recommend directed commercial cord blood collection and stem-cell storage in low-risk families".
The American Academy of Pediatrics has stated that cord blood banking for self-use should be discouraged (as most conditions requiring the use of stem cells will already exist in the cord blood), while banking for general use should be encouraged. In the future, cord blood-derived embryonic-like stem cells (CBEs) may be banked and matched with other patients, much like blood and transplanted tissues. The use of CBEs could potentially eliminate the ethical difficulties associated with embryonic stem cells (ESCs).
While the American Academy of Pediatrics discourages private banking except in the case of existing medical need, it also says that information about the potential benefits and limitations of cord blood banking and transplantation should be provided so that parents can make an informed decision.
In the United States, cord blood education has been supported by legislators at the federal and state levels. In 2005, the National Academy of Sciences published an Institute of Medicine (IoM) report which recommended that expectant parents be given a balanced perspective on their options for cord blood banking. In response to their constituents, state legislators across the country are introducing legislation intended to help inform physicians and expectant parents on the options for donating, discarding or banking lifesaving newborn stem cells. Currently 17 states, representing two-thirds of U.S. births, have enacted legislation recommended by the IoM guidelines.
The use of cord blood stem cells in treating conditions such as brain injury and Type 1 Diabetes is already being studied in humans, and earlier stage research is being conducted for treatments of stroke, and hearing loss.
Cord blood stored with private banks is typically reserved for use of the donor child only. In contrast, cord blood stored in public banks is accessible to anyone with a closely matching tissue type and demonstrated need. The use of cord blood from public banks is increasing. Currently it is used in place of a bone marrow transplant in the treatment of blood disorders such as leukemia, with donations released for transplant through one registry, Netcord.org, passing 1,000,000 as of January 2013. Cord blood is used when the patient cannot find a matching bone marrow donor; this "extension" of the donor pool has driven the expansion of public banks.
The umbilical cord in other animalsEdit
The umbilical cord in some mammals, including cattle and sheep, contains two distinct umbilical veins. There is only one umbilical vein in the human umbilical cord.
In some animals, the mother will gnaw through the cord, thus separating the placenta from the offspring. The cord along with the placenta is often eaten by the mother, to provide nourishment and to dispose of tissues that would otherwise attract scavengers or predators. In chimpanzees, the mother leaves the cord in place and nurses her young with the cord and placenta attached until the cord dries out and separates naturally, within a day of birth, at which time the cord is discarded. (This was first documented by zoologists in the wild in 1974.)
Animals that lay eggs seem to have a false umbilical-cord that attaches the embryo and yolk together in much the same way.
Other uses for the term "umbilical cord"Edit
The term "umbilical cord" or just "umbilical" has also come to be used for other cords with similar functions, such as the hose connecting surface-supplied divers to their surface supply of air and/or heating, or space-suited astronauts to their spacecraft. Engineers sometimes use the term to describe a complex or critical cable connecting a component, especially when composed of bundles of conductors of different colors, thickness and types, terminating in a single multi-contact disconnect.
Cancer-causing toxicants in human umbilical cordsEdit
In multiple American and international studies, cancer-causing chemicals have been found in the blood of umbilical cords. These originate from certain plastics, computer circuit boards, fumes and synthetic fragrances among others. Over 300 chemical toxicants have been found, including bisphenol A (BPA), tetrabromobisphenol A (TBBPA), Teflon-related perfluorooctanoic acid, galaxolide and synthetic musks among others. The studies in America showed higher levels in African Americans, Hispanic Americans and Asian Americans due, it is thought, to living in areas of higher pollution.
- "Umbilical – Search Online Etymology Dictionary". www.etymonline.com. Archived from the original on 4 March 2016. Retrieved 27 March 2018.
- "The Umbilical Cord". yale.edu. Archived from the original on 28 March 2013. Retrieved 27 March 2018.
- Meyer WW, Rumpelt HJ, Yao AC, Lind J (July 1978). "Structure and closure mechanism of the human umbilical artery". Eur. J. Pediatr. 128 (4): 247–59. doi:10.1007/BF00445610. PMID 668732. S2CID 37516644.
- Saleh, R; Reza, HM (10 October 2017). "Short review on human umbilical cord lining epithelial cells and their potential clinical applications". Stem Cell Research & Therapy. 8 (1): 222. doi:10.1186/s13287-017-0679-y. PMC 5634865. PMID 29017529.
- "Fetal Circulation". www.heart.org. Archived from the original on 22 December 2017. Retrieved 27 March 2018.
- Kiserud, T.; Acharya, G. (2004). "The fetal circulation". Prenatal Diagnosis. 24 (13): 1049–1059. doi:10.1002/pd.1062. PMID 15614842. S2CID 25040285.
- Mikael Häggström, MD (2020-08-27). Patholines https://patholines.org/Placenta. Missing or empty
- "Peculiarities in the Vascular System in the Fetus – Gray's Anatomy of the Human Body – Yahoo! Education". Archived from the original on January 23, 2012.
- Cohain, J. S. (2010). "A Proposed Protocol for Third Stage Management – Judy's 3,4,5,10 minute method". Birth. 37 (1): 84–85. doi:10.1111/j.1523-536x.2009.00385_2.x. PMID 20402731.
- Yao AC, Lind J, Lu T (1977). "Closure of the human umbilical artery: a physiological demonstration of Burton's theory". Eur. J. Obstet. Gynecol. Reprod. Biol. 7 (6): 365–8. doi:10.1016/0028-2243(77)90064-8. PMID 264063.
- Quan A, Leung SW, Lao TT, Man RY (December 2003). "5-hydroxytryptamine and thromboxane A2 as physiologic mediators of human umbilical artery closure". J. Soc. Gynecol. Investig. 10 (8): 490–5. doi:10.1016/S1071-5576(03)00149-7. PMID 14662162.
- White RP (January 1989). "Pharmacodynamic study of maturation and closure of human umbilical arteries". Am. J. Obstet. Gynecol. 160 (1): 229–37. doi:10.1016/0002-9378(89)90127-0. PMID 2912087.
- "Umbilical Cord Complications: eMedicine Obstetrics and Gynecology". Archived from the original on 2010-01-29. Retrieved 2010-01-24.
- P02.5 Fetus and newborn affected by other compression of umbilical cord Archived 2014-11-02 at the Wayback Machine in ICD-10, the International Statistical Classification of Diseases
- "Fetus or Newborn Problems: Labor and Delivery Complications: Merck Manual Home Edition". Archived from the original on 2010-03-28. Retrieved 2010-03-27.
- McDonald, SJ; Middleton, P; Dowswell, T; Morris, PS (Jul 11, 2013). "Effect of timing of umbilical cord clamping of term infants on maternal and neonatal outcomes". The Cochrane Database of Systematic Reviews. 7 (7): CD004074. doi:10.1002/14651858.CD004074.pub3. PMC 6544813. PMID 23843134.
- Stiegler, Paul M., M.D. (May 2007). "EMT-BASIC \ EMT BASIC INTERMEDIATE TECHNICIAN PROTOCOLS" (PDF). Dane County Emergency Medical Services. Archived (PDF) from the original on April 6, 2012. Retrieved December 17, 2011.CS1 maint: multiple names: authors list (link)
- Meersman, Jack. "EMT-B: Obstetrics, Infants and Children". Wild Iris Medical Education. Archived from the original on January 20, 2012. Retrieved December 17, 2011.
- McDonald, S. J.; Middleton, P.; Dowswell, T.; Morris, P. S. (2013). McDonald, Susan J (ed.). "Effect of timing of umbilical cord clamping of term infants on maternal and neonatal outcomes". The Cochrane Database of Systematic Reviews. 7 (7): CD004074. doi:10.1002/14651858.CD004074.pub3. PMC 6544813. PMID 23843134.
- Committee on Obstetric Practice, American College of Obstetricians and, Gynecologists (December 2012). "Committee Opinion No.543: Timing of umbilical cord clamping after birth". Obstetrics and Gynecology. 120 (6): 1522–6. doi:10.1097/01.aog.0000423817.47165.48. PMID 23168790.
- Committee on Obstetric Practice (2017-01-01). "Committee Opinion No. 684". Obstetrics & Gynecology. 129 (1): e5–e10. doi:10.1097/aog.0000000000001860. ISSN 1873-233X. PMID 28002310.
- Hutton EK, Hassan ES (March 2007). "Late vs early clamping of the umbilical cord in full-term neonates: systematic review and meta-analysis of controlled trials". JAMA. 297 (11): 1241–52. doi:10.1001/jama.297.11.1241. PMID 17374818.
- Examination of the Newborn & Neonatal Health: A Multidimensional Approach, p. 116-117
- "Effect of timing of umbilical cord clamping of term infants on maternal and neonatal outcomes." Cochrane Database Syst Rev. 2008; (2):CD004074
- Andersson, O; Lindquist, B; Lindgren, M; Stjernqvist, K; Domellöf, M; Hellström-Westas, L (1 July 2015). "Effect of Delayed Cord Clamping on Neurodevelopment at 4 Years of Age: A Randomized Clinical Trial". JAMA Pediatrics. 169 (7): 631–8. doi:10.1001/jamapediatrics.2015.0358. PMID 26010418.
- "Can delayed umbilical cord clamping reduce infant anemia at age 8, 12 months?". medicalxpress.com. Archived from the original on 25 February 2018. Retrieved 27 March 2018.
- Military Obstetrics & Gynecology – Delivery of the Baby Archived 2010-01-23 at the Wayback Machine The Brookside Associates Medical Education Division. Retrieved Jan 10, 2009
- Waterbirth International – Waterbirth FAQ Retrieved Jan 10, 2009
- Crowther, S (2006). "Lotus birth: leaving the cord alone". The Practising Midwife. 9 (6): 12–14. PMID 16830839.
- "Human Reproduction, Lectures: Clinical Genetics". Retrieved 2010-02-11.
- "Umbilical Cord Blood Banking" (PDF) (Scientific Impact Paper 8). Royal College of Obstetricians and Gynaecologists. 2006. Retrieved 2021-07-01.
- American Academy of Pediatrics. "Cord Blood Banking for Potential Future Transplantation". Archived from the original on 2007-10-13.
- "Cord blood yields 'ethical' embryonic stem cells." Archived 2008-10-10 at the Wayback Machine, Coghlin A. New Scientist, August 18, 2005. Accessed June 25, 2007.
- Cord Blood for Neonatal Hypoxic-Ischemic Encephalopathy Archived 2011-08-12 at Wikiwix, Autologous Cord Blood Cells for Hypoxic Ischemic Encephalopathy Study 1. Phase I Study of Feasibility and Safety
- Haller MJ; Viener, HL; Wasserfall, C; Brusko, T; Atkinson, MA; Schatz, DA; et al. (2008). "Autologous Umbilical Cord Blood Infusion for Type 1 Diabetes". Exp. Hematol. 36 (6): 710–715. doi:10.1016/j.exphem.2008.01.009. PMC 2444031. PMID 18358588.
- Vendrame M, et al. (2006). "Cord blood rescues stroke-induced changes in splenocyte phenotype and function". Exp. Neurol. 199 (1): 191–200. doi:10.1016/j.expneurol.2006.03.017. PMID 16713598. S2CID 29804539.
- Vendrame M, et al. (2005). "Anti-inflammatory effects of human cord blood cells in a rat model of stroke". Stem Cells Dev. 14 (5): 595–604. doi:10.1089/scd.2005.14.595. PMID 16305344.
- Revoltella RP, et al. (2008). "Cochlear repair by transplantation of human cord blood CD133+ cells to nod-scid mice made deaf with kanamycin and noise". Cell Transplant. 17 (6): 665–678. doi:10.3727/096368908786092685. PMID 18819255.
- Najjar, Dana (2020-12-18). "Should You Bank Your Baby's Cord Blood?". The New York Times. ISSN 0362-4331. Retrieved 2021-07-01.
- "Archived copy" (PDF). Archived (PDF) from the original on 2013-11-02. Retrieved 2013-04-13.CS1 maint: archived copy as title (link)
- Meat Hygiene. J. F. Gracey, D. S. Collins, Robert J. Huey. p. 32.
- See In the Shadow of Man, by Jane Goodall.
- "Sharks (Chondrichthyes)". FAO. Archived from the original on 2008-08-02. Retrieved 2009-09-14.
- Chen, Mei-Huei; Ha, Eun-Hee; Wen, Ting-Wen; Su, Yi-Ning; Lien, Guang-Wen; Chen, Chia-Yang; Chen, Pau-Chung; Hsieh, Wu-Shiun (3 August 2012). "Perfluorinated Compounds in Umbilical Cord Blood and Adverse Birth Outcomes". PLOS ONE. 7 (8): e42474. Bibcode:2012PLoSO...742474C. doi:10.1371/journal.pone.0042474. PMC 3411780. PMID 22879996.
- "Why Are Trace Chemicals Showing up in Umbilical Cord Blood?". Archived from the original on 2012-09-02. Retrieved 2012-09-01.
- Media related to Umbilical cord at Wikimedia Commons