出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/08/22 22:37:36」(JST)
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| Hypoplastic left heart syndrome | |
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Illustration of heart suffering from Hypoplastic left heart syndrome
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| Classification and external resources | |
| Specialty | medical genetics |
| ICD-10 | Q23.4 |
| ICD-9-CM | 746.7 |
| OMIM | 241550 |
| DiseasesDB | 31507 |
| MedlinePlus | 001106 |
| eMedicine | ped/1131 |
| MeSH | C14.240.400.625 |
Hypoplastic left heart syndrome (HLHS) is a rare congenital heart defect in which the left ventricle of the heart is severely underdeveloped.
In babies with HLHS, the aorta and left ventricle are underdeveloped before birth, and the aortic and mitral valves are either too small to allow sufficient blood flow or are atretic (closed) altogether. As blood returns from the lungs to the left atrium, it must pass through an atrial septal defect to the right side of the heart.
To see how a heart with HLHS varies from a healthy heart, see the graphics on the Cove Point site.[1]
In a healthy human, the left side of the heart receives oxygen-rich blood from the lungs and pumps it out to the rest of the body; with these structures underdeveloped, they cannot circulate blood to other organs, and the right ventricle must pump blood to both the lungs, as it would normally, and to the rest of the body, a situation which cannot be sustained for long.
In cases of HLHS, the right side of the heart often must pump blood to the body through a patent ductus arteriosus. As the ductus arteriosus usually closes within eleven days after birth, blood flow is severely restricted and eventually cut off, leading to dangerously low circulation and eventually to shock.
The majority of congenital heart defects have no known cause.[2][3] If part of the endocardial tube gets pinched shut in a region that becomes the future ventricle, hypoplastic heart syndrome will occur. If the pinched part of the endocardial tube is the bulbus-cordis region of the developing heart, hypoplastic RIGHT syndrome will occur. If it is in the ventricle region it will be the LEFT side that is hypoplastic.[4][5][6][7][8]
Colleagues at Cincinnati Children’s Hospital in Ohio studied 1,500 newborns from 38 children’s hospitals in the United States from the 1990s to 2006. They found that babies born between April and July were more likely to have this defect, establishing strong evidence that seasonality and [9] environmental factors play a significant role in causation.
HLHS usually occurs as an isolated cardiac defect. Genetic loci associated with HLHS include GJA1 (connexin 43), HAND1, NKX2.5, 10q, and 6q.[10][11] In addition to these specific genetic associations, predisposing mutations are thought to play a role in pathogenesis of HLHS because the recurrence risk in first degree relatives of infants with HLHS is 2-4%.[10] HLHS has been seen in the following genetic syndromes: Trisomy 13 (Patau syndrome), Trisomy 18 (Edwards syndrome), Partial Trisomy 9, Turner's syndrome, Jacobsen syndrome, Holt-Oram Syndrome, and Smith-Lemli-Opitz Syndrome.[10]
Without life-prolonging interventions, HLHS is fatal, but with intervention, an infant may survive. A cardiothoracic surgeon may perform a series of operations or a full heart transplant.
Before surgery, the ductus must be kept open to allow blood-flow using medication containing prostaglandin. Air with less oxygen than normal is used for infants with hypoplastic left heart syndrome. These low oxygen levels increases the pulmonary vascular resistance (PVR) and thus improve blood flow to the rest of the body, due to the greater pressure difference between the lungs and body. Achieving oxygen levels below atmosphere requires the use of inhaled nitrogen.[12] Nitric oxide is a potent pulmonary vasodilator, thus reduces PVR, improves venous return. Any factor that increases PVR will impede right sided flow.[13][14]
Surgical operations to assist with hypo-plastic left heart are complex and need to be individualized for each patient. A cardiologist must assess all medical and surgical options on a case-by-case basis.
Currently, infants undergo either the staged reconstructive surgery (Norwood or Sano procedure within a few days of birth, Glenn or Hemi-Fontan procedure at 3 to 6 months of age, and the Fontan procedure at 1 1/2 to 5 years of age) or cardiac transplantation.[15] Current expectations are that 70% of those with HLHS will reach adulthood.[16] Many studies show that the higher the volume (number of surgeries performed) at a hospital, the lower the mortality (death) rate.[17][18] Therefore, the main determinant of success is the choice of hospital. Other factors that increase an infant's risk include lower birth weight, additional congenital anomalies, a genetic syndrome or those with a highly restrictive atrial septum.[citation needed]) For patients without these additional risk factors, 5 year survival now approaches 80%.[citation needed] Further, studies show that about 50% of those children who survived surgery in the early development of staged reconstruction have developmental delay or need special education; about 25% of these surgical survivors have severe disabilities.[citation needed] There is growing evidence that while the incidence of developmental and behavioral disabilities continues to be higher than that in the general population, children operated upon in the more current era have shown significantly better neurological outcomes.[citation needed] An alternative to the traditional Norwood is the Hybrid procedure.[citation needed]
Some physicians offer "compassionate care", instead of the surgeries, which results in the child's death, usually within 2 weeks of birth. Compassionate care is overseen by a physician, and may be carried out either in the hospital or at home. However, due to the vast improvement of surgical intervention, with many hospitals achieving over 90% survival, there is debate on whether or not "compassionate care" should still be offered to families.[19] A study in 2003 concluded that a selection of physicians who are experts in the care of children with HLHS were evenly split when asked what they would do if their own children were born with HLHS, with 1/3 stating that they would choose surgery, 1/3 stating that they would choose palliative (compassionate) treatment without surgery, and 1/3 stating that they are uncertain which choice they would make.[20]
The three-stage procedure is a palliative procedure (not a cure), as the child's circulation is made to work with only two of the heart's four chambers.
The first step is the Norwood procedure. In this procedure, the right ventricle is used to pump blood into the systemic circulation. Since the right ventricle is no longer directly pumping blood to the lungs, a shunt is required in order to pass deoxygenated blood through the lungs. Either the subclavian artery can be connected to the pulmonary circulation (Blalock-Taussig shunt), or a shunt is made directly from the right ventricle to the pulmonary circulation (Sano shunt). The narrow aorta is enlarged using a patch to improve blood flow to the body.[21]
During this time the baby may be medically fragile and have feeding problems because the heart is working very hard. There is a considerable degree of venous mixing in the right ventricle, leading to lower oxygenation saturation. In addition, the Blalock-Taussig shunt and the Sano shunt both expose the lungs to systemic arterial pressures, leading in the long term to pulmonary hypertension and eventually to heart failure.
The Hybrid procedure is used in place of the Norwood. The Hybrid procedure does not necessitate the use of heart-lung bypass or performing a sternotomy. Instead of a six-hour surgery, the Hybrid typically takes one to two hours. In the procedure, a stent is placed in the Ductus Arteriosis to maintain its patency, and the Pulmonary Artery branches has bands placed over both right and left branches to limit pressure and over-circulation to the lungs.[22] Outcomes with the Hybrid approach are comparable with the Norwood.[23][24]
The second stage, the bi-directional Glenn procedure or Hemi-Fontan (see also Kawashima procedure) relieves some of the above problems. In this operation, the superior vena cava is ligated from the heart and connected to the pulmonary circulation. At this time, the Blalock-Taussig or Sano shunt is taken down. At this point, the lungs are no longer exposed to systemic arterial pressures, but much lower venous pressures. Although venous blood from the upper half of the body is no longer mixing with oxygenated blood in the right ventricle, there is still venous mixing from the lower half of the body, leading to some degree of oxygen desaturation.
During this time the child may have improved quality of life as the heart does not have to work as hard.[25]
The final procedure, the Fontan (Fontan procedure) completes the repair of the hypoplastic left heart. Although there are several variations, the functional effect is to redirect venous blood from the lower body (through the inferior vena cava) away from the right atrium to the pulmonary artery. Now, there should not be any mixing of oxygenated and deoxygenated blood in the right ventricle. The right ventricle performs the traditional job of the left, supplying the body with oxygenated blood, while the passive systemic venous pressure performs the traditional job of the right, passing deoxygenated blood to the lungs.
The Norwood Procedure is generally performed within a week of birth, the second stage at 3–6 months of age, and the Fontan at 18 months to four years of age.[citation needed] There are two types of Fontan: the Lateral Tunnel Fontan, and the Extracardiac Fontan.[citation needed] When the Fontan Procedure was first being done for children with HLHS, the only Fontan was the Lateral Tunnel Fontan.[citation needed] This requires actual cutting in the heart itself to create a "tunnel" by which the blood can travel passively to the lungs.[citation needed] Within the last decade, doctors have created an Extracardiac Fontan.[citation needed] This operation creates a tunnel outside the heart itself which reduces the chances of Fontan patients developing scar tissue on the heart which might later cause arrhythmias.[citation needed]
While infants successfully treated for HLHS have a good chance of survival, they may experience chronic health problems for the rest of their lives.[citation needed] The 3-stage surgeries were developed in the early 1980s with no survivors prior to that time.[citation needed] Therefore, the earliest survivors are in their early 30s and the long term prognosis is unknown.[citation needed] However, the advances in surgical and medical techniques have helped increase the survival rate dramatically since the surgeries were first developed.[citation needed]
As is true for patients with other types of heart defects involving malformed valves,[26] HLHS patients run a high risk of endocarditis, and must be monitored by a cardiologist for the rest of their lives to check on their heart function.
The three stage Norwood procedure only increases the life span of the heart as HLHS cannot be cured.[citation needed] A heart transplant may be needed at some point in the child's lifetime.[citation needed]
There is an extensive network of parents and children who have experienced this problem, and a number of targeted small press publications and websites.
Patients receiving the Fontan Procedure have an increased incidence of "Plastic Bronchitis."[citation needed]
The National Birth Defects Prevention Network estimates that birth defects occur in about three percent of live births in the United States. Of those birth defects, HLHS occurs in one out of 4,344 live births, or an estimated total of 960 live births every year in the United States.[27][28][29] HLHS occurs at a sixth of the rate of the most common birth defect, Trisomy 21 (Down syndrome).
Diagram of a healthy heart and one suffering from Hypoplastic left heart syndrome
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| リンク元 | 「左心低形成症候群」「unequivocally」「HLHS」 |
| 関連記事 | 「hearing」「left」「hear」「heart」「hypoplastic」 |
┌─体循環─┐
──右心室──┤ ├──
└─肺循環─┘
手術：Norwood手術、両側Glenn手術、Fontan手術
[★] 左心低形成症候群 hypoplastic left heart syndrome