Normal labour and delivery

Chapter 7 Normal labour and delivery





MYOMETRIAL ACTIVITY: PREGNANCY


During pregnancy the uterus is usually in a quiescent state. In the third trimester women experience low amplitude, poorly synchronised Braxton Hicks or practice contractions. Substances which contribute to the inhibition of myometrial activity include progesterone from placental syncytiotrophoblast and chorion; myometrial parathyroid hormone-related peptide; and nitric oxide and relaxin from the myometrium, decidua, chorion and amnion in addition to prostacyclins. The process of myometrial contraction requires activation of calmodulin, a calcium-binding protein with calcium ions which then in turn activates the enzyme myosin light chain kinase to produce adenosine triphosphate to power actin and myosin filaments to slide over each other to produce shortening. Inhibitors of myometrial activity act by increasing intracellular levels of cyclic nucleotides to prevent release of calcium ions from intracellular stores or by reducing myosin light chain kinase activity.


Towards term a number of processes occur which predispose to activation or preparation of the myometrium for onset of labour. Formation of gap junctions by increases in contraction-associated proteins such as connexin-43 enhance cell to cell coupling. Receptors for oxytocin and stimulatory prostaglandins are also increased. These changes are associated with myometrial stretch when the uterus enlarges and with the higher levels of oestrogens derived partly from placental conversion of fetal dehydroepiandrosterone (DHEAS) where they also exert a local oestrogen effect. In addition to increased DHEAS production, activation of the fetal hypothalamic–pituitary–adrenal axis in late pregnancy results in more fetal cortisol biosynthesis. Fetal cortisol competes to reduce the local progesterone effect and stimulate synthesis of corticotrophin-releasing hormone from placenta and fetal membranes for production of prostaglandins by the latter structures.



MYOMETRIAL ACTIVITY: LABOUR


Initiation of labour remains unclear, but prostaglandins have been implicated in myometrial contraction. Isoforms of phospholipase A2 or C, activated by varying requirements for calcium ions, liberate arachidonic acids from membrane phospholipids. Prostaglandin synthase in amnion and chorion convert arachidonic acids to primary prostaglandins. For prostaglandin E2 (PGE2) there are four main receptor subtypes labelled from EP-1 to EP-4. These receptors are distributed in the myometrium in varying concentrations. Stimulation of EP-1 and EP-3 results in contractions whereas stimulation of the other two receptors leads to relaxation. These together with corticotrophin-releasing hormone-related cyclic AMP in the lower uterine segment contribute to fundal dominance.


Onset of labour is associated with a substantial increased myometrial sensitivity to oxytocin stimulation and a three- to five-fold increase in oxytocin production by chorio-decidual tissue. Oxytocin raises concentrations of free calcium in the myocytes to promote myometrial contraction.


Fetal membranes covering the internal cervical os exhibit a decreased production of the 15-hydroxyprostaglandin dehydrogenase enzyme which metabolises prostaglandins. More local prostaglandin production is available for cervical effacement and dilatation. This effect is supplemented by release of collagenase through increased cytokine activity.


Onset of labour is most likely between midnight and 0500 hours when maternal secretion of oxytocin peaks and the myometrium is most sensitive to oxytocin and prostaglandin. These changes in steroid and protein concentrations return to non-pregnant levels 48–72 hours post partum.



Uterine work


Myometrial contraction exerts a pull in circular and longitudinal directions (Figure 7.1)



The term fundal dominance is used to describe travel of myometrial contractions from the fundus of the uterus towards the cervix. The starting point or pacemaker for myometrial activity is situated near the point of insertion of the fallopian tubes into the uterus. The spread of myoelectrical activity through the uterus requires 1 minute. Approximately another minute is needed for adequate relaxation. Blood vessels must traverse the myometrium to reach the placenta. Contractions occurring more than once every 2 minutes contribute to poor myometrial relaxation and reduce blood and hence oxygen supply to the fetus. When two contractions are noted every 10 minutes for an hour consider possible onset of labour. In established labour the rate of contractions ranges between 3 and 5 per 10 minutes.


In early labour the uterus is not working at maximum capacity. This may be because the number of myometrial cells contracting is limited or contraction is poorly synchronised or of short duration. As labour progresses contractions becomes more efficient and uterine work increases. Capacity for work cannot, however, increase indefinitely. A stable phase for ability to work results once maximal work output is achieved for the individual mother. When the stable phase is achieved (Figure 7.2a) additional stimulation by oxytocics is of little value and can be harmful. Uterine work has been expressed as:






Mar 16, 2017 | Posted by in NURSING | Comments Off on Normal labour and delivery

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