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BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES 2005; 5 (1): 14-18

&

Abstract

Ductal dependent congenital heart diseases represent -  of all congenital heart diseas-es. A primary goal of the treatment of these diseases is to retain ductus open until the fi nal cardiosurgical treatment. Prostaglandins are presently the only medicaments, which have a capability to keep ductus open. By means of a retrospective study in a period from Janu-ary,  until December,  at the Paediatric clinic of the Clinical centre of the Univer-sity in Sarajevo,  patients (treated with prostaglandins) diagnosed with ductal dependent congenital heart diseases were analyzed. In our sample, there are / male patients (. ), / (.) were full-term newborns, while / (. ) were eutrophic at birth. An average saturation increase, after the prostaglandin therapy, measured in blood from the capillaries is , and measured transcutanlly is  units. Duration of prostaglandin therapy in our study was on average . days. Th e most common cause of death was insuffi cien-tia cardiorespiratoria ( out of ), but sepsis/infection ( out of ) and insuffi cientia re-nalis were also common. .  ( out of ) patients died partly because of the complex-ity of these diseases, but also because a cardiosurgical treatment is delayed. A goal of this study is evaluation of saturation with oxygen before and after the prostaglandin therapy.

KEY WORDS: saturation, duct dependent, congenital heart disease, prostaglandin

Saturation With

Oxygen for Ductal

Dependent Congenital

Heart Diseases

Before and After the

Prostaglandin Therapy

Senka Dinarević*, Hajrija Maksić, Majda Haznadar

Paediatric clinic of the Clinical Centre of the University of Sarajevo, Bolnička ,   Sarajevo, Bosnia and Herzegovina

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BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES 2005; 5 (1): 14-18

Introduction

Congenital cardiac diseases have an incidence of .  () and ductal dependent congenital heart diseases are represented with -  (). Ductus arteriosus in a foetal period exists as a large vascular structure, with a diameter equal to lung truncus and descending aorta. About -  of foetus systemic circulation fl ows from the right to the left side of circulation through ductus. Lung resistance decreases with a first breath intake, ductus constriction starts and it is functionally closed - hours after the birth. Structural closure of duc-tus usually ends between the  th and the . day (). Newborns with ductal dependent congenital heart diseases can be symptomatic until the moment duc-tus closes, so a number of children are sent home as healthy. Decrease of blood flow through duc-tus causes dangerous hypoxia or cardiogenic shock, metabolic acidosis, multisystemic failure and death. Ductal dependent congenital heart diseases con-sist of the following congenital heart disease groups:

A. Ductal dependent pulmonary circulation: pul-monary atresia with intact intraventricular septum, tetralogia Fallot (more serious forms), tricuspid atre-sia, univentricular heart with critical stenosis or with pulmonary artery atresia;

B. Ductal dependent systemic circulation: hypoplas-tic left heart syndrome, crihypoplas-tical aorhypoplas-tic stenosis, criti-cal aortic coarctation, aortic arch obstruction; C. Ductal dependent congenital heart diseases

with-out an adequate blood mixing: transposition of great arteries.

A common order of therapeutic measures for the above stated heart diseases is prostaglandin therapy, intubation and sedation, oxygen therapy, correction of acidosis, hypoperphusion and hypotension (,,) A primary goal for the patients with ductal dependent

congenital heart diseases is to medicamently retain their ductus open. Prostaglandins are presently the only medicaments, which keep ductus open. Th e usu-al starting dose is . to . mcg/kg/BW*/min, and a maintenance dose is lower and can be as low as . mcg/kg/BW/min in a continuous infusion. The drug side-effects are numerous, and some of them are: ap-noea, convulsions, vasodilatation, arrhythmia, hypo-tension, fever, infection, hypoglycaemia, hypocalcae-mia, bleeding, thrombocytopenia and diarrhoea (,).

Patients and Methods

During the period from January,  until December, ,  patients who were treated with prostaglan-dins at the Paediatric clinic of the Clinical centre of the University in Sarajevo, neonatology unit, with ducal de-pendent congenital heart diseases have been analyzed by a retrospective study. A source of information were patient records (disease histories) and computer infor-mation bases. Diagnosis for heart disease in all cases was obtained with an echocardiography, after the his-tory, physical fi ndings, ECG, lung and heart X-rays, and a complete blood analysis with the acidobasic status (ABS). Th e group was analyzed according to sex, birth weight, weeks of gestation, time duration of prostaglan-din therapy, fi nal outcome and a death cause. All the patients received Alprostadil (prostaglandin E) in-travenously in a continuous infusion. Saturation with oxygen before and after the prostaglandin therapy was recorded transcutanly and from capillary blood.

Results

A total of  patients formed this study. Males were pre-sented with  (/) which has been shown in Table . Out of a total number of newborns with ductal

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BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES 2005; 5 (1): 14-18

dent congenital heart diseases - .  (/) were eu-thropic (Graph ). Considering that oxygen exchange until birth is conducted through mother’s placenta (as most important role), it is not a surprise that all the patients were well developed for their age at birth. An average increase of saturation after the prostaglandin therapy followed via gases analyses of capillary blood was  units, ranging from  to  (Table ). From the same Table it is visible that increase of transcutan

saturation was  units, ranging from  to  units as well as an average maintenance dose of prostaglandins: . mcg/kg/BW/min (from . to .). Table  rep-resents data on an average duration of prostaglandin therapy was . days ranging from  to  days. Out of  patients,  of them died (.), and the three who survived were transferred to the cardiosurgical centres outside of Bosnia and Herzegovina. In Table : causes of death: four patients (. ) died due to cardiac in-sufficiency, three died due to systemic infection and three because of renal insufficiency. In one newborn cause of death was massive intracranial haemorrhage.

Discussion

Usage of prostaglandins goes back to the ’s. The Nobel prize for a research on prostaglandins in  won Von Euler, and in  Suneu K. Bergstrom, John R.Vane. Th e drug Alprostadil - prostaglandin E is in use in neonatal cardiology, but also Dinoprost - pros-taglandin E. All the patients in our study received Al-prostadil by infusion. However, use of prostaglandin E is recommended by Silove, because he found that they have fewer side-eff ects (). Unwanted eff ects are in a close correlation with a dose. Th e most common com-plications are apnoea, febrile states and infection. Silove

0 2 4 6 8 10 12

>2500 4000-2500

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BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES 2005; 5 (1): 14-18

recommends . mcg/kg/BW/min, while larger doses are given for a few hours at the beginning. An average maintenance dose in our study is . mcg/kg/BW/min. Prostaglandins directly eff ect smooth muscles of ductus arteriosus and dilate it. Th ey cause vasodilatation of all the arterioles. Th ey inhibit aggregation of platelets. A maximum effect of the drug occurs after  minutes from the start of infusion for cyanotic, and after a few hours for the obstructive lesions. Th ey have to be given before ductus closes completely, because this drug can-not open it. An eff ectiveness of the drug depends on the starting values of pO; the more serious hypoxia is, the more pO increases. Th us, we can say that age of a child and starting values of pO have a key role in ef-fectiveness of the drug. A way of drug intake (venous or arterial), sex or pCO do not aff ect the drug eff ective-ness (,,). In our study,   (/) of the children started the prostaglandin therapy on the fi rst day of life. An average increase of saturation measured in capillary blood was  units, ranging from  to  units. An av-erage increase of saturation measured transcutanly was  units, ranging from  to . Prostaglandins are given for a relatively short period of time, a few hours to a few days, longest for a month. During that time, a child is cardiosurgically cared for. If a duration of the therapy is prolonged, side-eff ects are more common and more serious, and ductus becomes very brittle, so that during

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BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES 2005; 5 (1): 14-18

Conclusion

This randomized, clinically selected study confirms a justifi cation for the use of prostaglandins in neonatal cardiology, and their useful effect. However, in or-der to increase a survival rate and life quality of these patients, it is necessary to improve and to establish a proper paediatric cardiosurgery in Bosnia and Herze-govina. Cardiosurgery in Bosnia has been improved during the past four years, which can be seen in a total number ( patients) and outcomes (figures in

co-relation with European centres) of the treated patients by the local team and the cardiosurgeons from Austria. However, improvement concerns primarily a continuos prostaglandin supply, education in the foetal echocar-diology (which would signifi cantly decrease a number of complex congenital heart diseases) and a paediat-ric cardiosurgery, so that the patients with congenital heart diseases can have an adequate treatment on time.

() Montana E., Khoury M.J., Cragan J.D., Sharma S., Dhar P. D. Trends and outcomes after prenatal diagnosis of congenital car-diac malformations by foetal echocardiography in well defi ned birth population. Atlanta, Georgia, - J. Am. Coll. Cardiol. ; : -.

() Mitchell S.C., Korneus S.B., Bereendes H.W. Congenital heart dis-ease in . births: Incidence and natural history. Circulation ;:.

() Avery, G. et al. Neonatology - pathophysiology and management of the Newborn. Lippincott – Raven Publishers; ; -. () Dinarević S., Kurtagić S., Maksić H. Th e application of

prostaglan-dins in neonatal cardiology. Journal of physicians, dentists and pharmacists of Bosnia and Herzegovina. ;  (-): -. () Grubbs T.C., Kraft N.L. Neonatal transport issues with

prosta-glandin E infusions. Air Med J. ; ():-.

() Saxena A., Sharma M., Kothari S.S., Juneja R., Reddy S.C., Sharma R., Bhan A., Venuqopal P. Prostaglandin E in infants with con-genital heart disease: Indian experience. Indian Pediatr. ; ():-

() Borow K., Green L.H., Castaneda A.R., et al. Left ventricular func-tion after repair of tetralogy of Fallot and its relafunc-tionship to age at repair. Circulation ; :

() Peled N., Dagan O., Babyn P., Silver MM., Barker G., Hellmann J., Scolnik D., and Koren G. Gastric-outlet obstruction induced by prostaglandin therapy in neonates. Th e N. Engl. J. Med. ; : -

() Pfl ieger K., Patent ductus arteriosus. Instant access to the minds of medicine. Lake Point Medical Center ; -

() Carter E.L., Garzon M.C. Neonatal urticaria due to prostaglandin E.Pediatr Dermatol. ;():-.

() Newburger J.W., Silbert A.R., Buckley L.P., Fyler D.C. Cognitive function and age at repair of transposition of the great arteries in children. N. Engl. J. Med. ; :

() Joshi A., Berdon W.E., Brudnicki A., LeQuesne G., Ruzal-Shapiro C., Hayes C. Gastric thumbprinting: diff use gastric wall mucosal and submucosal thickening in infants with ductal-dependent cya-notic congenital heart disease maintained on long-term prosta-glandin therapy. Pediatr Radiol. ; ():-.

References

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