- Case Report
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Post mortem coronary angiography in a preemie heart – a case report
Journal of Congenital Cardiology volume 3, Article number: 8 (2019)
Postmortem coronary angiography has been used in forensic medicine for several decades but its use has never been documented in neonatal hearts. The objective of this case is to report the use of postmortem coronary angiography as a diagnostic modality for neonates suspected to have complex congenital heart anomalies.
A 36-week-old female infant required extracorporeal membranous oxygenation for persistent hypotension on day 1 of life. A congenital echocardiogram (ECHO) on day 3 of life revealed multiple anomalous vascular structures within the interventricular septum. The infant passed away on day 4 of life after the parents elected to withdraw support. A consent for autopsy was taken from the parents and a postmortem coronary angiography was performed. The coronary vessels were injected with Iodixanol contrast via a 24 G angiocath under fluoroscopy. The anomalous septal vessels were identified as dilated coronary artery and vein. No other anomalies were identified.
Postmortem coronary angiography complements other imaging procedures in understanding the nature of some complex congenital heart defects and in determining the cause of death in such neonates.
What is already known about this subject?
Coronary angiography is a well-known modality in the pediatric and adult cardiology would.
What does this study add?
The use of coronary angiography as a tool in postmortem examination/autopsies of neonatal hearts has not been documented in the past; It can be a useful tool in helping understand complex congenital heart disease.
How might this impact on clinical practice?
Post mortem coronary angiography can be an adjunct to other diagnostic imaging modalities in postmortem examinations to help improve our understanding of complex congenital heart lesions.
Postmortem examinations are vital for the understanding of some complex cardiac lesions that may not be clearly seen by echocardiography (ECHO). With the recent advances in science, many institutions are performing postmortem CT angiography routinely for cases with sudden death [1, 2]. Postmortem coronary angiography has been utilized in forensic medicine for several decades . It helps to ascertain unusual anatomic variations like aneurysms and anastomoses. We report a case of postmortem coronary angiography performed on a neonatal heart.
A 2080 g female infant was born at 36 weeks via C-section due to fetal distress. The pregnancy was complicated by intrauterine growth retardation, suspected fetal arrhythmia, abnormal fetal ultrasound (suspected Ebstein’s anomaly of the tricuspid valve), multiple maternal viral syndromes and poor prenatal care (late entry into the United States at 31 weeks’ gestation, prior care in El Salvador). Apgar scores were 1, 3, 4 at 1, 5, and 10 min, respectively. Despite adequate ventilation and fluid resuscitation, the infant remained hypotensive and had profound metabolic acidosis (arterial pH of 6.56). Prostaglandins were started in addition to inotropes. Echocardiogram (ECHO) in the first few hours of life revealed a poor left ventricular function (shortening fraction of 11.8%), a severe biventricular hypertrophy and a moderate size patent ductus arteriosus (PDA) with a bidirectional shunt. There was a moderate to severe tricuspid regurgitation (peak gradient of 75 mmHg) with severe pulmonary hypertension (estimated right ventricular pressure of 80 mmHg). Otherwise normal four chamber intra-cardiac anatomy. The infant was placed on veno-arterial extracorporeal membranous oxygenation (ECMO) at 6 h of life. A repeat ECHO on the third day of life showed improved LV function (SF 25%), severe pulmonary hypertension (estimated right ventricular pressure of 90 mmHg), a small apical muscular ventricular septal defect (VSD) with a right to left and multiple vascular structures within the ventricular septum (Fig. 1, Additional file 1: Video S1). These structures were suspected to be coronary fistulas, dilated coronary vessels or unusual VSD tracts within the ventricular septum . The infant subsequently developed a grade 4 intraventricular hemorrhage and passed away on the fourth day of life. Work up for common infectious causes of congenital infections was negative. Genetic evaluation revealed a normal 46 XX karyotype and a negative cardiomyopathy panel.
Due to the ambiguity of the vascular structures in the ECHO, a consent for an autopsy was obtained from the parents. The autopsy showed severe biventricular hypertrophy, a small apical muscular VSD and a dilated left main left anterior descending (LAD) coronary arteries. Otherwise, the gross anatomy of the heart was normal (Fig. 2a).
Post-mortem coronary angiography
During the initial autopsy examination, the ventricular cavities were opened by para-septal incisions and the origin of the LAD was severed. Therefore, the LAD was cannulated with a 24 G Angiocath (Fig. 2a). Initially, a 5 ml of normal saline was injected to clear the coronary artery from blood clots. An oozing of saline from the cut surface of the myocardium into both ventricle was noted. Then, 0.3 ml of Iodixanol (Visipaque 320, GE Healthcare) contrast was injected in the LAD and an angiogram was obtained (Fig. 2b). This showed a normal branching pattern of the distal LAD without any evidence of fistulous drainage into the LV apex. Because of the damage of LAD during the autopsy, we decided to inject contrast into the coronary sinus to delineate the coronary venous anatomy. The coronary sinus was cannulated and the catheter was advanced to the middle coronary vein where a 0.3 ml of Iodixanol contrast was injected. The middle coronary vein was remarkably dilated and its tributaries opacified and there was also a late opacification of distal branches of LAD (Fig. 3). This further confirmed that there were no abnormal coronary venous structures or fistulas that may have been missed in the prior angiogram of the LAD.
Based on these images, it was concluded that the prominent coronary artery and vein were secondary to severe ventricular hypertrophy. There was no evidence of a coronary fistula.
Discussion & Conclusions
To our knowledge, this is the first report of postmortem coronary angiography on a neonatal heart. This study highlights the significance of a collaborative effort between cardiology and pathology in answering questions for neonates with an unclear cause of death or complex congenital cardiac anomalies especially if the patient is not stable enough before death to go through a cardiac MRI or catheterization.
Several contrast media have been used for postmortem angiography. These include corpuscular radiopaque contrast materials (lead oxide and barium sulfate), oily liquids (paraffin oil, diesel oil), hydrosoluble preparations (Gastrograffin, cardiografin) and Casts (silicon rubber-lead oxide) with each associated with its own pros and cons . One study suggested the use of colored dyes mixed with Gastrograffin and using different colors for the right and left coronary arteries in order to help with delineation during subsequent macroscopic and microscopic examinations . We used Iodixanol (Visipaque 320), a contrast agent commonly used in coronary angiography due to its favorable properties .
We describe a methodology for performing postmortem coronary angiography in neonatal heart specimen. We recommend that angiograms be performed prior to dissection of the heart to maintain the integrity of the coronary arteries that can facilitate cannulation and injection of contrast. This procedure may complement other imaging procedures in understanding the nature of some complex congenital heart defects and in determining the cause of death.
Availability of data and materials
Extracorporeal membranous oxygenation
Left anterior descending
Ventricular septal defect
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Ethics approval and consent to participate
Ethics approval was obtained from the institution prior to performing the autopsy. Since this was a case report without any identifying information, an IRB approval was not required.
Consent for publication
Consent for publication was obtained from the parents of the patient (neonate) verbally and a written consent was obtained for the autopsy/post-mortem coronary angiography.
The authors declare that they have no competing interests.
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Cite this article
Qasim, A., Balaguru, D. & Aly, A.M. Post mortem coronary angiography in a preemie heart – a case report. J Congenit Heart Dis 3, 8 (2019). https://doi.org/10.1186/s40949-019-0029-2
- Pediatric cardiology
- Coronary angiography
- Cardiac pathology
- Diagnostic imaging
- Forensic pathology