Saturday, November 22, 2008

Best Children's Hospitals

Makenna and Her Transformed Heart: No Slowing Her Down

After three surgeries in four years, Makenna and her redesigned pump are ready for anything

Posted May 29, 2008

Makenna Franks turns 5 this month. She'll probably start dance class soon. She noshes on Fritos twists, chases after her older brother and her boy cousins, and tries to climb trees the way they can in her suburban Houston neighborhood. Just a regular kid. But less than a year ago, she was on the operating table at Texas Children's Hospital for the third open-heart surgery of her four-year life.

Makenna photo gallery
Makenna Franks, nine months after her third surgery.
Makenna Franks, nine months after her third surgery.
Makenna Franks, nine months after her third surgery.
Makenna Franks, nine months after her third surgery.

Makenna was born with hypoplastic left heart syndrome, which affects about 1 in every 3,000 to 6,000 babies. In "hypoplasts," as doctors call these children, the left ventricle—the heart's main pumping chamber—and the aorta, which carries oxygenated blood to the body, stop developing before birth. Two of Makenna's heart valves also were defective.

Even as recently as the mid-'90s, most HLHS babies died. Gradually, however, a small group of surgeons has worked out a complex three-stage repair in which major vessels are rebuilt and rerouted to shift pumping chores to the right side of the heart. At Texas Children's, the death rate is now below 2 percent.

Makenna had the first stage as a 3-day-old infant and the second one at six months. Last August, Charles Fraser, chief of congenital heart surgery, performed the final step, which U.S. News chronicled in "Makenna's Heart" [September 3].

Recuperation wasn't fun. Her lymphatic system leaked fatty fluid into her lungs and around her heart, so Makenna was kept on a no-fat diet for six weeks after surgery. No Fritos. "Her big day was when she could finally eat those things," says pediatric cardiologist Michelle Grenier of Texas Children's, who has seen Makenna more than 10 times, most recently last month to run a battery of tests. "We want to watch these kids very, very closely," she says—measuring their blood oxygen, for example, to make sure their reworked hearts are pumping enough oxygenated blood.

The replumbed heart is working well, says Grenier. She pronounces her patient "just amazing—she knows she has a zipper on her chest, but she won't let it slow her down." Nor does Grenier think she should. "One of our concerns with our cardiovascular patients is that parents have a tendency to baby them, worry about them playing too hard, maybe feeding them a little too indulgently. Can she dance? Ride a bike? You bet."

Bobby and Brandi Franks aren't take-it-easy-sweetie parents. "We don't limit her," says Bobby. Nor do they assume that their daughter's life will now be perfectly normal. "Along the way I'm sure there will be bumps, and we'll do what needs to be done," says her father.

A recent study in the journal Circulation suggests that Makenna has a good shot at a smooth road. Researchers tracked every Children's Hospital Boston patient born prior to 1985 who had Makenna's type of surgery. Most, even those who had the procedure many years ago, were alive 20 and 25 years later.

"If Makenna came to me as a teenager and asked if she could run a marathon," says Grenier, "I would tell her she probably could—if she'd been doing as remarkably well as she has so far."

Reader Comments

MY LITTLE ANGEL WITH HLHS

MY DAUGHTER WILL BE 9 ON MARCH 26,2009. SHE WAS DIAGNOSED WITH HLHS AT 5 DAYS OLD. SHE HAD HER NORWOOD AT 10 DAYS,HEMI FONTAN AT 6 MTHS, AND HER FONTAN AT 18 MTHS. HER SURGERIES WERE DONE IN ANN ARBOR,MICHIGAN,BY DR. EDWARD BOVE.HE IS THE DR. THAT PIONEERED THE HEMI FONTAN SURGERY AND SINCE THEN THESE STAGE OF SURGERIES HAVE BEEN MORE SUCCESSFUL.HE WORKED WITH DR. NORWOOD BEFORE GOING OUT ON HIS OWN.HE HAS DONE MORE OF THESE SURGERIES THAN ANY OTHER DR. I HIGHLY RECOMMEND HIM TO FIX UP YOUR LITTLE ONE IF YOUR LOOKING FOR A SURGEON. MY DAUGHTER IS VERY HEALTHY AND CAN KEEP UP WITH ANY CHILD HER AGE PHYSICALLY AND MENTALLY. I WAS READING ONE OF THE STORIES ABOUT A PARENT OR DR. LETTING A HLHS CHILD HAVE NO LIMITATIONS. YOU HAVE TO REMEMBER THESE KIDS HEARTS OVERWORK JUST TO LIVE SO THEY SHOULD BE LIMITED TO OVER DOING IT BECAUSE IF THEY WEAR THEIR HEART OUT THE ONLY THING LEFT IS A NEW HEART AND THERE NOT EASY TO FIND!!!! MY DAUGHTER TAKES 1 2.5 ENALAPRIL AND 1 BABY ASPIRIN A DAY.GOD HAS BLESSED HER WITH A SPECIAL GIFT OF MUSIC SO WE DONT HAVE TO WORRY ABOUT SPORTS. SHE HAS BEEN IN PIANO FOR 4 YEARS AND SINGS IN HER DADDYS COUNTRY BAND SINCE SHE WAS 5.

re: My 2nd unborn son

Reading the last comment brought me back one year ago. Our unborn daughter was diagnosed on October 12, 2007 with hypoplastic left heart syndrome too. She was due on Feb 22, 2008 and arrived a little early on Valentine's Day. We have survived 2 open heart surgeries and 2 heart caths. Her cardiologist tells us she is doing amazing! People are amazed when we tell them she has had 2 open heart surgeries. She isn't any different than any other 8 month olds (other than her "zipper"). I hope our story can offer some hope to you and others out there. We have a caringbridge site under nevaehw if you would like to read more.

My 2nd unborn son

My wife is pregnant with our second son. When we found out that we were pregnant in June, we were estatic. Then recently, we found out that it was a boy and were also told that he has HLHS. We are both very very scared and am hoping for a miracle tbat he is alright when he is born. We are both christians and believe that God can heal anyone. It would be great if that is the case but we both are also looking at the possibility of having to go through the 3 surgeries. We live in Charlotte NC and will be going to CMC and the Levine Children's hospital to have our surgeries. I don't know why this happened but all I know is that God has his plan for our Jake and he will be fine. It will be a long and very difficult journey for us which will test us as christians and also test our strength as a family. We are due 02/20/2009.

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