Care4Conway: Home

Thursday, May 13, 2010

Home

Versed makes me so giddy!

Monkers got an ID bracelet too!

"I so tired."

"All done Dr. Bromberg's Hospital."

It was a long day but went well, I'd say. Arrived at 9:45 am and got discharged around 6:30 or so. They weren't in any hurry to get rid of him b/c of his cardiac history. The anesthesiologist was even going to admit him if it made us more comfortable. We all felt better giving him as much time as he needed and given how much morphine and benadryl that he received, he needed a lot of time just to be able to hold his head up and keep his eyes open longer than a few seconds! He woke up pretty discombobulated in the recovery room but settled down pretty well once they got me back there to see him. I got to hold him and rock him the rest of the hour and then back to the pre-op holding area. He drank a total of 2.5 small cans of sprite and ate doritos and teddy grahams. All was fine until we got on the highway heading home in a torrential downpour when he vomited all over. And I mean ALL OVER! So far he's not been sick again and we're crossing our fingers it's out of his system. The big problem now is going to be keeping him safe. We absolutely must to keep him from reinjuring that arm. Today Dr. Stazzone was able to do a closed reduction, but if this happens again he'll have to make an incision and put rods or pins in the bone. Today he might have even done that but he weighed the risks of potential cardiac complications with extended surgery time and decided that the alignment he was getting was good enough. He referred to the way the bones are placed now as "bayonetting"; meaning that they are not perfectly straight, but one is a little elevated and parallel. He says if it stays this way he'll heal just fine and have no long term problems. We go back in another week to make sure the bone is still in the right place. He says he'll have the cast at least another month and then he's putting him in a brace for a month. We're praying that we can keep him from acting like a boy for at least the next two weeks so that this bone can calcify some and harden.

He got tons of compliments on how well he handled the day. They say most three year olds don't do nearly that well. God sure blessed us, didn't he?

1 comment:

Anonymous said...: Yes, God blessed you with a beautiful boy who is obviously very precious to Him as well as to you. I pray that all continues to go well, and that good solid healing takes place. Try to get some rest for yourself as well!
Love to you as always. Sr J; May 15, 2010 at 9:07 PM

Conway's Heart Story

Conway's Heart Story

Conway David Beckemeier was born on March 3, 2007. His heart defects went undetected during pregnancy and he was diagnosed at two days of age with L-TGA, a large VSD, sub pulmonic stenosis and Ebstein’s Anomaly. Just before turning six months of age, he underwent open heart surgery to reroute the bloodflow in his heart. Called the "double switch", this procedure is the most technically challenging for pediatric cardio-thoracic surgeons to perform. The version of the double switch that Conway received on 8/28/07 was called the Rastelli-Senning with VSD closure and sub pulmonic resection. He suffered a grand mal seizure following the surgery that lasted over an hour and had several other post-op setbacks including surgical heart block, which required another operation on 9/18/07 to insert a pacemaker. Following surgery and such a long hospital stay, Conway developed an oral aversion (he would not eat) and he was 100% NG tube fed for eight months. He also lost muscle tone and required both physical and occupational therapies. In April 2008, he had a cardiac cath and attempted balloon angioplasty on his pulmonary arteries that did not work. Although his recovery was very long, he had a solid year or so of being a "normal" kid . Then in May of 2009, it was discovered that Conway was having rhythm disturbances, specifically atrial flutter. His pacemaker allowed it to go undetected for several weeks until he showed signs of heart failure and was admitted to the ICU for a week to be placed on IV heart meds and undergo cardioversion on 5/6/09. He went home and his heart function started recovering when he had another episode of flutter (6/16/09). This time, he was again hospitalized and put on IV milrinone, but he converted back to normal sinus rhythm by himself. At that time he was placed on the anti-arrhythmia drug, amiodarone. On 7/22/09 he had to be cardioverted again for yet another episode of flutter. The following week, he got worse instead of better. His cardiologist did a full work up and it was determined that his aortic, mitral and tricuspid valves were all leaking worse and were felt to be the cause of his heart failure. On 8/24/09 he had a cardiac cath and attempted ablation. The electrophysiologist was unable to induce a single arrhythmia. Then, just two days later, he went into atrial flutter on his own. He was placed back in the cath lab where he underwent mapping and a total of 17 burns were made to try to knock out his arrhythmias for good. The next day, 8/27/09, he had his second open heart surgery to repair his mitral valve called ring annuloplasty. He also had a partial Maze procedure done. His surgeries are performed at C.S. Mott Children’s Hospital at the University of Michigan (Ann Arbor). This time he was discharged just six days later! His Left Ventricular function improved drastically. In December 2010 we noticed he began getting more winded during physical activity. A January 2011 cath showed that he is outgrowing his RV-PA gortex conduit, but he was not symptomatic enough to warrant intervention. In April 2012 Conway’s fatigue increased and an echo at the end of May revealed that the ratio between the right and left sided pressures has gotten too high and it is time to replace the homograft that was placed when he was five months old. He had a cardiac cath on 5/25/12 which confirmed the echo findings. He had surgery on 8/8/12 to replace his pulmonary valve and RV-PA conduit, add an additional pacing wire to his left ventricle, and change his generator to a bi-ventricular model which is shown to preserve function and help the heart muscle pump more efficiently/effectively.