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1 КАЗАХСКИЙ МЕДИЦИНСКИЙ IУНИВЕРСИТЕТ НЕПРЕРЫВНОГО ОБРАЗОВАНИЯ
Вестник АГИУВ № 3, 2017
УДК 616.31-053.2
A.Mullen1 у К. Abzaliyev2, Ghazwan Butrous3
'Kazakh National Medical University, S.D. Asfendiyarov, Almaty, Kazakhstan -Kazakh Medical University of Continuous Education, Almaty, Kazakhstan. 'University of Kent, Kent, United Kingdom
ULTRASOUND FACILITIES IN PREDICTING PULMONARY ARTERIAL HYPERTENSION IN CHILDREN WITH CONGENITAL
LEFT-TO-RIGHT SHUNTING
SUMMARY
Pulmonary arterial hypertension (PAH) in children with congenital left-to-right shunt (APAH - CHD) is a very common complication. The question of the indications forthe cardiac surgery repair of the left-to-right shunt is controversial and has no one solution. In Scientific Centre of Paediatric and Paediatric Surgery (SCP and PS) of the Ministry of Health of the Republic of Kazakhstan since 2011 department of the cardiac surgery and intervention cardiology treats over 120 children with APAH - CHD. The most part of the patients is older 6-month-old.However, the guidelines for ventricular septal defect (VSD), patent ductus arteriosus (PDA) and atrial septal defect (ASD) are not define the precise moment of the surgery repair. Early terms for these types of CHD agreed to be under 2 years old.Aforementioned, we studied the evidence of Echocardiography parameters in predicting PH in children with congenital left-to-right shunting on the early age. For that we took the Echo reports of 26 children from 60 to 186 days of life with congenital left-to-right shunting, under suspicious of being complicated with pulmonary arterial hypertension. For the main objective of our study we assessed the volume overload with measure of Qp/Qs index, peak and mean velocity and pressure gradients of the tricuspid regurgitation (TR) and on the pulmonary artery (PA) systolic flow. Size of the aorta (Ao) and PA.16 children (group 1) were operated at the age of 11.5±4.2 months old, while other 10 (group 2) were operated at the age of 3.6±1.3 years old. 19 children were with VSD, and 8 with PDA. Children with the high EDI and Qp/Qs ratio show more tendency for developing PAH in postoperative period.
Key words: pulmonary arterial hypertension, congenital heart diseases, children, echocardiography.
Background. Pulmonaryhypertension (PH) isapathophysiological condition that may involve various clinical conditions and can complicate cardiovascular (such as congenital heart defects (CHD) and respiratory diseases. The term PAH includes a group of PH patients characterized haemodynainically by the presence of pre-capillary PH, defined by a pulmonary artery wedge pressure (PAWP) < 15 mmHg and a PVR >3 Wood units (WU) in the absence of other causes of precapillary defined by right heart catheterization [1]. PAH in children with congenital left - to - right shunt (APAH - CHD) is a very common complication [2-3]. Although, PAH has a strong impact on the cardiac surgery outcomes. But due to invasive method of diagnostic process makes it painful and not safe for children, especially under 6 months old. The question of the indications for the cardiac surgery repair of the left-to-right shunt
is controversial and has no one solution [4-6].
Echocardiography (Echo) is non-invasive, accessible and reasonable tool for assessment of heart structures and function. Likewise, Echo gives a lot of information about complications, such as PAH [7-9].
In Scientific Centre of Paediatric and PaediatricSurgery (SCP and PS) of the Ministry of Health of the Republic of Kazakhstansince 2011 department of the cardiac surgery and intervention cardiology treats over 120 children with APAH -CHD. The most part of the patients is older 6-month-old. While the shunt was presented and diagnosed in their newborn. However, the guidelines for ventricular septal defect (VSD), patent ductus arteriosus (PDA) and atrial septal defect (ASD) arc not define the precise moment of the surgery repair. Early terms for these types of CHD agreed to be under 2 years old [10-11].
Aforementioned facts lead to the aim of our study.
Aim: to evaluate the evidence of Echocardiography parameters in predicting PH in children with congenital left-to-right shunting on the early age.
Materials and methods: we studied the Echo reports of 26 children from 60 to 186 days of lifewith congenital left-to-right shunting, under suspicious of being complicated with pulmonary arterial hypertension. All children were admitted to SCP and PS between 2012 and 2016. Echo was performed by the standard paediatric protocol with the segmental analysis of heart and great vessels [8,12-13].
For the main objective of our study, we assessed the volume overload with measure of Qp/Qs index, peak and mean velocity and pressure gradients of the tricuspid regurgitation (TR) and on the pulmonary artery (PA) systolic flow. Size of the aorta (Ao) and PA.
Results: Among the total numberofchildren, there were no gender ratio difference. Equal number of boys and girls were registered. 16 children (group 1) were operated at the age of 11.5±4.2 months old, while other 10 (group 2) were operated at the age of 3.6±1.3 years old.19 children were with VSD, and 8 with PDA. Clinical status was defined as average. BMI was 16.2±1.3, no poor feeding. All kids had no additional pathologies or premorbid conditions.
Initial measurements of the shunt's size were interpreted as large. Hemodynamicstatus of the VSD patients had next characteristics: mean Qp/ Qs ratio was 1.32±0.14, interventricular gradient wasmoderate (42±8.3 mm.Hg.),VSD/Ao ratio was 0.72±0.11. Mean right ventricle systolic pressure (RVSP) was 46.2±9.3 mm.Hg. PA and Ao sizes were normal with the z-score 1.1 ±0.12. One
general index for all patients that was increased is left ventricle (LV) end diastolic index(EDI), what was 83.2±17.5. This we interpreted as LV dilation. RV was preserved and not dilated.
Echo measurements at the surgery time were different from initial in both groups. However, group 2 showed significant evidences of PH presence compared to group 1. Mean RVSP for the group 1 was 48±16.2 mm. Hg, while for the group 2 it was 56.7±18.2 (p value=0.0236). In the group 1 z-score for PA had not been changed, nonetheless in group 2 z-score increased to 1.9±0.6, while the Ao z-score remained the same (p value =0.0371). Correlation between mean RVSP and VSD/Ao ratio was not significant (p-value= 0.0782). Qp/Qs ratio raised up to 3.2±0.84 for group 2.
After the surgery repair of the left-to right shunt Echo measurements were taken again. For group 1 there were no evidence for PAH. Mean RVSP was 23.8±8.2 mm.Hg., what was statistically significant decreasing (p value = 0.0031 ). For group 2 mean RVSP fell down only for 7 children to the level of 36±2.6 mm.Hg., what is in the "grey" zone by definition. 3 patients demonstrated PAH presence after cardiac surgery with mean RVSP 47.5±6.8 mm.Hg. (p value = 0.0455).EDI reduced for both groups to 48.7±14.5 (p value = 0.0285).
Conclusion: the criteria for the timing of surgery repair of the congenital left-to-right shunting in children under 1 year old, requires a number of considering factors. Echo is the best for non-invasive examination. Children with the high EDI and Qp/Qs ratio show more tendency for developing PAH in postoperative period. Doppler ultrasound facilities using hemodynamic parameters can show high level of evidence for predicting pulmonary hypertension in children with congenital left-to-right shunting.
REFERENCES
1 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS)Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT) // Eur. Heart J. - 2015. - P. 317.
2 Silva L.M. et al. KinCor, a national registry for paediatric patients with congenital and other types of heart disease in the Netherlands: aims, design and interim results // Neth. Heart J. - 2016.
3 Barrows F.A., Rabinovitch M. The pulmonary circulation in children with congenital heart disease: morphologic and morphometric considerations 11 Can. Anaesth. Soc. J. - 1985. - Vol. 32, no. 4. - P. 364-373.
1 КАЗАХСКИЙ МЕДИЦИНСКИЙ IУНИВЕРСИТЕТ НЕПРЕРЫВНОГО ОБРАЗОВАНИЯ
Вестник АГИУВ № 3, 2017
4 Roofthooft M. T. R., Loon R. L. E. van. Berger R.M.F Management of pulmonary arterial hypertension in children // Paediatr. Respir. Rev. - 2010. - Vol. II, no. 4. - P. 240-245,
5 Lopes A.A., O'Leary P.W. Measurement, interpretation and use of haemodynamic parameters in pulmonary hypertension associated with congenital cardiac disease // Cardiol. Young. - 2009. - Vol. 19, no. 5. - P. 431-435.
6 Beghetti M. et al. Haemodynamic characterisation and heart catheterisation complications in children with pulmonary hypertension: Insights from the Global TOPP Registry (tracking outcomes and practicc in pacdiatric pulmonary hypertension) // Int. J. Cardiol. - 2016. - Vol. 203. - P. 325-330.
7 Ebeid M.R., Ferrer P.L., Robinson B., Weatherby N.. Gebland H. Doppler echocardiography evaluation of pulmonary vascular resistance in children with congenital heart disease // J. Am. Soc. Echocardiogr. Off. Publ. Am. Soc. Echocardiogr. - 1996. - Vol. 9, no. 6. - P. 822-831.
8 Markley R.R., Ali A., Potfay J., Paulsen IV., Jovin I.S. Echocardiography Evaluation of the Right Heart // J. Cardiovasc. Ultrasound. - 2016. - Vol.24, no. 3. - P. 183-190.
9 Ploegstra M.-J. et al. Echocardiography in pediatric pulmonary arterial hypertension: early study on assessing disease severity and predicting out come // Circ. Cardiovasc. Imaging. - 2015. - Vol. 8, no. 1.
10 Amedro P. et al. Quality of Life of Children with Congenital Heart Diseases: A Multicenter Controlled Cross-Sectional Study // Pcdiatr. Cardiol. - 2015. - Vol. 36, no. 8. - P. 1588-1601.
11 Falcone N. Pulmonary hypertension in pediatric heart surgery // Rev. Esp. Anestesiol. Reanim. - 2001. - Vol. 48, no. 10. - P. 462-464.
12 Anderson R. H., Shirali G. Sequential segmental analysis // Ann. Pediatr. Cardiol. - 2009. Vol. 2, no. 1. - P. 24-35,
13 Cheitlin M.D. et al. ACC/AHA Guidelines lor the Clinical Application of Echocardiography // Circulation. - 1997. - Vol. 95, no. 6. - P. 1686.
АННОТАЦИЯ
Легочная артериальная гипертензия (ЛАГ) у детей с врожденным лево-правым шунтированием крови (АЛАГ - ВПС) является очень распространенным осложнением. Проблема определения показаний к хирургической коррекции порока противоречивая и не имеет единого решения. В Научном центре педиатрии и детской хирургии Министерства здравоохранения Республики Казахстан с 2011 г. функционирует отделение кардиохирургии и интервенционной кардиологии, где пролечено более 120 детей с АЛАГ - ВПС. Большая часть пациентов младше 6 месяцев. Однако руководства по ведению дефекта межжелудочковой перегородки (ДМЖП), открытого артериального протока (ОАП), и дефекта межпредсердной перегородки (ДМПП) не определяют точный возраст для проведения коррекции. Ранним оперативным вмешательством при ВПС данного типа считается возраст до 2-х лет.Исходя из вышеизложенного, нашей целью стало изучение информативности эхокардиографических (ЭхоКГ) параметров для прогнозирования ЛАГ у детей раннего возраста с врожденным лево-правым шунтированием крови. Для этого мы проанализировали 26 протоколов ЭхоКГ детей в возрасте от 60 до 186 дней, у которых диагностировали ВПС и подозревали ЛАГ.Для основной цели исследования оценили объемную перегрузку с измерением индекса Ор/Оэ, пиковых и средних скоростей и градиентов давления трикуспидальной регургитации (ТР) и систолического потока легочной артерии (ЛА). Размер аорты (Ао) и ЛА. 16 детей (группа 1) были прооперированы в возрасте 11,5±4,2 месяца, в то время как другие 10 (группа 2) прооперированы в возрасте 3,6±1,3года. 19 детей были с ДМЖП и 8 с ОАП.Дети с высоким конечным диастолическим индексом и Ор/Оэ демонстрируют выраженную тенденцию к развитию ЛАГ в послеоперационном периоде.
Ключевые слова: легочная артериальная гипертензия, врожденные пороки сердца, дети, эхокарди-ография.
ТШН
Балалардагы туа б1ткен канньщ сол-оц шунттауы бар екпе артериялык гипертензиясы (ЭАГ) (АЛАГ -ВПС) ете кен тараган аскыну болып табылады. Акауды хирургиялык тузету керсеттмдерт аныктау мэсе-лес1 карама-кайшылыкка толы жэне б1рде 6\р шеимм1 жок. Казакстан Республикасы Денсаулык, сактау министрлИ Педиатрия жэне балалар хирургиясы гылыми орталыгында 2011 жылдан бер1 кардиохирургия жэне интервенциялык кардиология белш жумыс ¡стейд1, мунда АЛАГ - ВПС диагнозы бар 120 аса бала
емделдк Наукастардыц кепштИ 6 айдан жотары жастаты балалар. Алайда карынша аральщ калка ака-уларын (КАКД), ашьщ артерияльщ акауларын (AAA) карау бойынша жетекштк карынша аральщ калка акауларына (КАКД) тузету журпзу ymiH накты жасты аньщтай алмайды. Аталтан типтеп ВПС кезЫде ерте оперативл араласута 2 жастан жотары жастатылар алынады. Жотарыдаты айткандарды ескере отырып, б1здщ максатымыз - балалардаты туа б1ткен канныц сол-оц шунттауы бар екпе артерияльщ гипертензи-ясын болжау ymiH эхокардиографияльщ (ЭхоКГ) параметрлердщ акпараттылытын зерделеу. Ол ушш 6i3 ВПС диагнозы койылтан жэне 0АГ кудкл 60 куннен 186 кунге дей1нг1 жастаты балалардыц 26 ЭхоКГ хаттамаларына талдау жасадьщ. Зерттеудщ непзп максатына жету ушш Qp/Qs индексш, шыцдьщ жэне орташа жылдамдытын, трикуспидалды регургитация (TP) кысымыныц градиентш, екпе артериясыныц (0А) систололальщ атымын, колка жэне 0А елшемдерш елшей отырып, келемд1 жуктемесш баталадьщ. 16 балата (1-топ) 11,5 ± 4,2 айльщ жасында ота жасалды, будан баска 10 балата (2-топ) 3,6±1,3 жасында жасалды. 19 балата КДКД жэне 8 балата AAA диагнозы койылтан. Жотары тупкшкл диастологияльщ индекс! жэне Qp/Qs балалар отадан кейшп кезецде 0АГ дамуыныц накты ypfliciH керсетедк
Туйшд1 сездер: туа б1ткен журек акауыныц екпе артерияльщ гипертензиясы, балалар, эхокар-диография.
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