Bladder exstrophy: Nursing

Bladder exstrophy is a congenital malformation where the bladder protrudes outside of the abdomen due to an abdominal wall defect.

First, let’s quickly review the embryological development of the bladder. The renal system, including the bladder, starts developing during week 4 of intrauterine life. At that point, the embryo is made up of three primitive germ layers: the ectoderm, the mesoderm and the endoderm. Towards the end of week 4 of development, the endoderm in the hindgut, which is the last portion of the primitive digestive tract, begins to expand forming the cloaca. The cloaca is a temporary structure connecting the urinary, digestive, and reproductive ducts.

By week 7, a wall of tissue called the urorectal septum forms in the cloaca and splits it into a posterior anorectal canal for the digestive tract, and an anterior urogenital sinus for genital and urinary structures. And the top portion of the urogenital sinus stretches out to form the primitive bladder. Ultimately, the cloacal membrane opens to the outside of the body for these structures to have openings. Now, at around the same time in development, the muscles and connective tissue of the lower anterior abdominal wall also begin to form.

Alright now, bladder exstrophy occurs when there is a midline closure defect during fetal development. Although the exact cause remains unknown, several risk factors have been identified. These include having a family history of bladder exstrophy, being white, or being assigned male sex at birth. This condition is also more common in infants born through assisted reproductive technology, such as in vitro fertilization, or IVF.