Cost and Optimal Surgery Time for Treating Pediatric Hypospadias Phallic Type

My child is 3 years old and has just had surgery. I want to ask, since there is still a catheter inserted, my child keeps complaining and wants it removed. There is no need to remove the catheter when a hypospadias patient is discharged from the hospital. Generally, the incision heals well within about a week after surgery, and the condition is stable, allowing the catheter to be taken out of the hospital. It is recommended that after discharge, pay attention to keeping the urethra unobstructed, drink plenty of water, and observe the urine for its color, clarity, turbidity, and blood presence. If there is a blockage or rupture of the ureter (both ends of the ureter need to be brought back to the hospital), please return to the hospital within 3 weeks to remove the catheter. The catheter can be removed after surgery or at a local hospital.

How long does it take for a child to fully recover after hypospadias surgery?

Enuresis and the Treatment of Pediatric Hypospadias

Pain may occur after pediatric hypospadias surgery, and it is important to monitor the child’s urination and wound condition to prevent infection.

Post-operation situation of pediatric hypospadias and surgery waiting list.

Hypospadias is a common congenital abnormality in boys, and surgical treatment is the only method. The purpose of the surgery is to correct penile curvature, bring the urethral opening as close to the normal position as possible, allowing children to stand and urinate, and have reproductive ability as adults. The surgery should be completed before the age of school entry. If there is associated with poor penile development, treatment with chorionic gonadotropin hormone can be used for 1-2 courses until the penile size reaches pre-surgery level. The actual cost of the surgery varies depending on the severity of the condition and the region.

Solutions for Pediatric Hypospadias

The Formation and Treatment Methods of Pediatric Hypospadias

Hypospadias is a congenital abnormality of the male urethral opening. It can cause an abnormal position of the urethral opening, curvature of the penis, urinary abnormalities, and sexual dysfunction, all of which require surgical treatment. If symptoms have not been completely resolved, it is recommended to undergo another surgery around the age of three or four.