INCREASED PULMONARY BLOOD FLOW IN NEWBORNS WITH CYANOTIC CONGENITAL HEART DEFECTS AND DUCTUS-DEPENDENT PULMONARY BLOOD FLOW: RESULTS AND FEATURES OF OUTPATIENT POSTOPERATIVE FOLLOW-UP

Aim. In patients with cyanotic congenital heart defects, pulmonary blood flow is maintained by a functioning patent ductus arteriosus (PDA). Most patients with complex duct-dependent cyanotic defects require intermediate palliative treatment before proceeding of total repair. Timely and complex outp...

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Main Authors: Anzhelika Mykhailovska, Olga Borodinova, Raad Tammo
Format: Article
Language:English
Published: Danylo Halytsky Lviv National Medical University 2024-10-01
Series:Acta Medica Leopoliensia
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Online Access:https://amljournal.com/index.php/journal/article/view/401
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author Anzhelika Mykhailovska
Olga Borodinova
Raad Tammo
author_facet Anzhelika Mykhailovska
Olga Borodinova
Raad Tammo
author_sort Anzhelika Mykhailovska
collection DOAJ
description Aim. In patients with cyanotic congenital heart defects, pulmonary blood flow is maintained by a functioning patent ductus arteriosus (PDA). Most patients with complex duct-dependent cyanotic defects require intermediate palliative treatment before proceeding of total repair. Timely and complex outpatient monitoring by a pediatrician and pediatric cardiologist are important for patient survival following palliative treatment, along with determining optimal timing for consultations at specialized cardiac surgical centers. To present the outcomes of two methods for increasing pulmonary blood flow (systemic-to-pulmonary artery shunt (SPAS) and stenting of patent ductus arteriosus (PDA st.)), as well as the features of outpatient cardiological observation and treatment in these patients. Materials and Methods. From 2000 to February 2024, 22 patients underwent SPAS (SPAS group), and stenting of patent ductus arteriosus was performed on 27 patients (PDA st. group) at the Ukrainian Cardiac Center. Results and Discussion. After interventions, the mean arterial oxygen saturation (SatO2) significantly increased in both groups, with a significantly higher improvement in the PDA st. group (p<0.05). The median average period of stay in ICU for the SPAS group was 15 [10.25; 24.75] days (from 5 to 91 days), for the group of PDA st. - 10 [7; 19,25] days (from 4 to 37 days) and was shorter in the group of PDA st. (p=0.05), and the duration of mechanical ventilation in the SPAS group was 254 [39.5; 471] hours (from 63 to 751 hours), and in the group of PDA st. was shorter - 134 [92.75; 158.7] (from 39 to 549 hours) (p<0.05). Early (30-day) postoperative mortality in the SPAS group accounted 13.6% (3 patients), with a late mortality of 18% (4/22). In contrast, there was no early (30-day) postoperative mortality in the PDA st. group, and late mortality accounted for 7,4% (2/27). Before the subsequent stage of surgical correction, sufficient growth of pulmonary artery branches was noted (Nakata index increased from 156.9±33.3 mm2/m2 to 277±35.9 mm2/m2 in the SPAS group and from 142.7±55.2 mm2/m2 to 289.1±149.2 mm2/m2 in the PDA st. group, and the left ventricular end-diastolic dimension index increased from 51.2±32.4 mm2/m2 to 67.5±15.5 mm2/m2 in the SPAS group and from 50.8±24.9 mm2/m2 to 56.7±28.5 mm2/m2 in the PDA st. group. Thirteen patients in the SPAS group underwent the next stage of surgical correction (Glenn shunt or total repair), while 19 patients in the PDA st. group received the next stage of surgical correction. Conclusions. Our study has demonstrated that both described methods are sufficiently effective for managing duct-dependent pulmonary blood flow in neonates with cyanotic CHD. Currently, due to the lower mortality rate associated with PDA stenting in neonates, it is the preferred option. However, for unfavorable ductal anatomy and in patients with CHD requiring prolonged postponement of the next surgical stage, SPAS remains more optimal choice. Careful monitoring by pediatricians and pediatric cardiologists during the interstage period is critically important.
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spelling doaj-art-8aa7680caf9d42c68ce8e38fa36b6b222025-01-06T10:49:52ZengDanylo Halytsky Lviv National Medical UniversityActa Medica Leopoliensia1029-42442415-33032024-10-01301-29310810.25040/aml2024.1-2.093401INCREASED PULMONARY BLOOD FLOW IN NEWBORNS WITH CYANOTIC CONGENITAL HEART DEFECTS AND DUCTUS-DEPENDENT PULMONARY BLOOD FLOW: RESULTS AND FEATURES OF OUTPATIENT POSTOPERATIVE FOLLOW-UPAnzhelika Mykhailovska0Olga Borodinova1Raad Tammo2Ukrainian Cardiac Center, Kyiv, Ukraine, Department of ultrasound and functional diagnosticUkrainian Cardiac Center, Kyiv, Ukraine, Department of consultative polyclinicUkrainian Cardiac Center, Kyiv, Ukraine, Department of RadiotherapyAim. In patients with cyanotic congenital heart defects, pulmonary blood flow is maintained by a functioning patent ductus arteriosus (PDA). Most patients with complex duct-dependent cyanotic defects require intermediate palliative treatment before proceeding of total repair. Timely and complex outpatient monitoring by a pediatrician and pediatric cardiologist are important for patient survival following palliative treatment, along with determining optimal timing for consultations at specialized cardiac surgical centers. To present the outcomes of two methods for increasing pulmonary blood flow (systemic-to-pulmonary artery shunt (SPAS) and stenting of patent ductus arteriosus (PDA st.)), as well as the features of outpatient cardiological observation and treatment in these patients. Materials and Methods. From 2000 to February 2024, 22 patients underwent SPAS (SPAS group), and stenting of patent ductus arteriosus was performed on 27 patients (PDA st. group) at the Ukrainian Cardiac Center. Results and Discussion. After interventions, the mean arterial oxygen saturation (SatO2) significantly increased in both groups, with a significantly higher improvement in the PDA st. group (p<0.05). The median average period of stay in ICU for the SPAS group was 15 [10.25; 24.75] days (from 5 to 91 days), for the group of PDA st. - 10 [7; 19,25] days (from 4 to 37 days) and was shorter in the group of PDA st. (p=0.05), and the duration of mechanical ventilation in the SPAS group was 254 [39.5; 471] hours (from 63 to 751 hours), and in the group of PDA st. was shorter - 134 [92.75; 158.7] (from 39 to 549 hours) (p<0.05). Early (30-day) postoperative mortality in the SPAS group accounted 13.6% (3 patients), with a late mortality of 18% (4/22). In contrast, there was no early (30-day) postoperative mortality in the PDA st. group, and late mortality accounted for 7,4% (2/27). Before the subsequent stage of surgical correction, sufficient growth of pulmonary artery branches was noted (Nakata index increased from 156.9±33.3 mm2/m2 to 277±35.9 mm2/m2 in the SPAS group and from 142.7±55.2 mm2/m2 to 289.1±149.2 mm2/m2 in the PDA st. group, and the left ventricular end-diastolic dimension index increased from 51.2±32.4 mm2/m2 to 67.5±15.5 mm2/m2 in the SPAS group and from 50.8±24.9 mm2/m2 to 56.7±28.5 mm2/m2 in the PDA st. group. Thirteen patients in the SPAS group underwent the next stage of surgical correction (Glenn shunt or total repair), while 19 patients in the PDA st. group received the next stage of surgical correction. Conclusions. Our study has demonstrated that both described methods are sufficiently effective for managing duct-dependent pulmonary blood flow in neonates with cyanotic CHD. Currently, due to the lower mortality rate associated with PDA stenting in neonates, it is the preferred option. However, for unfavorable ductal anatomy and in patients with CHD requiring prolonged postponement of the next surgical stage, SPAS remains more optimal choice. Careful monitoring by pediatricians and pediatric cardiologists during the interstage period is critically important.https://amljournal.com/index.php/journal/article/view/401congenital heart defectscyanosisincreasing the pulmonary blood flowstentpalliation
spellingShingle Anzhelika Mykhailovska
Olga Borodinova
Raad Tammo
INCREASED PULMONARY BLOOD FLOW IN NEWBORNS WITH CYANOTIC CONGENITAL HEART DEFECTS AND DUCTUS-DEPENDENT PULMONARY BLOOD FLOW: RESULTS AND FEATURES OF OUTPATIENT POSTOPERATIVE FOLLOW-UP
Acta Medica Leopoliensia
congenital heart defects
cyanosis
increasing the pulmonary blood flow
stent
palliation
title INCREASED PULMONARY BLOOD FLOW IN NEWBORNS WITH CYANOTIC CONGENITAL HEART DEFECTS AND DUCTUS-DEPENDENT PULMONARY BLOOD FLOW: RESULTS AND FEATURES OF OUTPATIENT POSTOPERATIVE FOLLOW-UP
title_full INCREASED PULMONARY BLOOD FLOW IN NEWBORNS WITH CYANOTIC CONGENITAL HEART DEFECTS AND DUCTUS-DEPENDENT PULMONARY BLOOD FLOW: RESULTS AND FEATURES OF OUTPATIENT POSTOPERATIVE FOLLOW-UP
title_fullStr INCREASED PULMONARY BLOOD FLOW IN NEWBORNS WITH CYANOTIC CONGENITAL HEART DEFECTS AND DUCTUS-DEPENDENT PULMONARY BLOOD FLOW: RESULTS AND FEATURES OF OUTPATIENT POSTOPERATIVE FOLLOW-UP
title_full_unstemmed INCREASED PULMONARY BLOOD FLOW IN NEWBORNS WITH CYANOTIC CONGENITAL HEART DEFECTS AND DUCTUS-DEPENDENT PULMONARY BLOOD FLOW: RESULTS AND FEATURES OF OUTPATIENT POSTOPERATIVE FOLLOW-UP
title_short INCREASED PULMONARY BLOOD FLOW IN NEWBORNS WITH CYANOTIC CONGENITAL HEART DEFECTS AND DUCTUS-DEPENDENT PULMONARY BLOOD FLOW: RESULTS AND FEATURES OF OUTPATIENT POSTOPERATIVE FOLLOW-UP
title_sort increased pulmonary blood flow in newborns with cyanotic congenital heart defects and ductus dependent pulmonary blood flow results and features of outpatient postoperative follow up
topic congenital heart defects
cyanosis
increasing the pulmonary blood flow
stent
palliation
url https://amljournal.com/index.php/journal/article/view/401
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AT olgaborodinova increasedpulmonarybloodflowinnewbornswithcyanoticcongenitalheartdefectsandductusdependentpulmonarybloodflowresultsandfeaturesofoutpatientpostoperativefollowup
AT raadtammo increasedpulmonarybloodflowinnewbornswithcyanoticcongenitalheartdefectsandductusdependentpulmonarybloodflowresultsandfeaturesofoutpatientpostoperativefollowup