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Table of Content Volume 7 Issue 3 - September 2018



A study of single umbilical artery and its associated findings at tertiary health care centre

 

Raju P

 

Assistant Professor, Department of Radiology, RVM Institute of Medical Sciences , Mulugu, Siddipet, Telangana, INDIA.

Email: rajpeddi9@gmail.com

 

Abstract               Background: Nearly 1 in 100 liveborn fetuses are diagnosed with single umbilical artery (SUA) Aims and Objectives: To Study Single Umbilical artery and its associated findings at tertiary health care centre. Methodology: After approval from institutional ethical committee a cross-sectional study was carried out in the department of Radiology of a tertiary health care centre during the two year period i.e. May 2016 to April 2018. This was a record based study all the sonography report were assesed to find out Single Umbilical artery and its associated findings or anomaly if present or not. Here all the anomaly scans were performed by Expert radiologists and by Color Doppler machines. All the reports were entered in the excel sheets and Analyzed by SPSS 19 version software for windows. Result: Out of 9870 all anomaly scan done in two years duration 80 were diagnosed as with Single Umbilical artery (SUA) so the prevalence of SUA in our study was 0.81% or 8.1 per one thousand anomaly scans done. The majority of the scans were with no associated anomaly or abnormal findings i.e. 67.5% followed by IUGR were 40%, Uro-genital anomalies were 16.25%, Cardiovascular anomalies were 15%, CNS anomalies were 11.25%, Skeletal were 8.75%, and GIT anomalies were 6.25%. The association of IUGR was 67.5 and 0.73%, Uro-genital anomalies -16.25 and 0.32, Cardiovascular anomalies -15% and 0.29%, CNS anomalies -11.25% and 0.20%, Skeletal- 8.75% and 0.17%, GIT anomalies -6.25% and 0.13% overall the presence of abnormal findings were significantly higher in SUA group as compared to Non SUA group (χ2 =1701, df=6, p<0.0001). Conclusion: It can be concluded from our study that the prevalence of SUA was 0.81%The majority of the scans were with no any associated anomaly i.e. 67.5% followed by IUGR were 40%, overall the presence of anomalies were significantly higher in SUA group as compared to Non SUA group

Key Words: SUA (Single Umbilical Artery), Foetal Anomaly Scan, IUGR (Intrauterine Growth Restriction), Urogenital anomalies, Cardio vascular anomalies, Gastro Intestinal Tract( GIT), CNS (Central Nervous System).

 

 

 

INTRODUCTION

Nearly 1 in 100 liveborn fetuses are diagnosed with single umbilical artery (SUA) and yet no consensus exists regarding the clinical relevance of this finding.1-3 Clinicians have long suspected an association between SUA and findings of intrauterine growth restriction (IUGR), preterm delivery, stillbirth, and congenital anomalies. Several studies have detected associations between SUA and adverse fetal outcomes to varying degrees. Some show not only an increased incidence of prematurity and IUGR in SUA babies but also a higher incidence of renal anomalies.4,5So we have done this study with the aim to see the prevalence of various anomalies and abnormal findings in comparison to non SUA group.

 

MATERIAL AND METHODS

After approval from institutional ethical committee a cross-sectional study was carried out in the department of Radiology of a tertiary health care centre during the two year period i.e. May 2016 to April 2018. This was a record based study all the sonography report were assessed to find out Single Umbilical artery and its associated anomaly if present or not. Here all the anomaly scans were performed by expert radiologists and by color Doppler machine. All the reports were entered in the excel sheets and Analyzed by SPSS 19 version software for windows.
RESULT

Out of 9870 all anomaly scan done in two years duration 80 were diagnosed as with Single Umbilical artery (SUA) so the prevalence of SUA in our study was 0.81% or 8.1 per one thousand anomaly scans done.

 

Table 1: Distribution of the SUA foetus with respect to radiological diagnosis

Radiological Findings

No. (n=80) *

Percentage (%)

No any anomaly

54

67.5

IUGR

32

40

Uro-genital

13

16.25

Cardiovascular

12

15

CNS

9

11.25

Skeletal

7

8.75

GIT

5

6.25

*(More than one radiological features/ anomalies were present so total may be more than 80)

The majority of the scans were with no any associated anomaly i.e. 67.5% followed by IUGR were 40%, Uro-genital were 16.25%, Cardiovascular were 15%, CNS were 11.25%, Skeletal were 8.75%, GIT were 6.25%.

Table 2: Distribution of the SUA and Non SUA Scans with respect to Anomaly

Radiological Findings

SUA (n=80)

Non-SUA (n=9790)

No any anomaly

54 (67.5)

9798 ( 99.27)

IUGR

32(40)

72 (0.73)

Uro-genital

13 (16.25)

32 (0.32)

Cardiovascular

12 (15)

29 (0.29)

CNS

9 (11.25)

20(0.20)

Skeletal

7 (8.75)

17(0.17)

GIT

5 (6.25)

13 (0.13)

(χ2 =1701, df=6, p<0.0001)

 

 

 

 

 

 

 

 

 

The findings or anomalies like IUGR was 67.5 and 0.73%, Uro-genital -16.25 and 0.32, Cardiovascular -15% and 0.29%, CNS -11.25% and 0.20%, Skeletal- 8.75% and 0.17%, GIT-6.25% and 0.13% overall the presence of abnormal findings were significantly higher in SUA group as compared to Non SUA group (χ2 =1701, df=6, p<0.0001)

 

DISCUSSION

The absence of one umbilical artery, defined as a single umbilical artery (SUA), is found in 0.2-1.9% of deliveries.5,6,7, A number of studies have reported that the presence of SUA may be related to a variety of congenital anomalies of the major organ systems as well as to chromosomal defects, aneuploidy, preterm delivery, and low birth weight. Incidence estimates from various populations (which may suffer from selection biases) range from 0.2-0.87%, with an associated anomaly rate reported to be as high as 67%.8-10 With the advent of color Doppler USG, umbilical arteries can be imaged in the amniotic cavity and in the fetal pelvis as they course around the bladder. Detection of SUA by USG is a potentially useful marker for suspecting an anomalous fetus. The three theories about the pathogenesis of SUA are (1) primary agenesis of one of the umbilical arteries, (2) secondary atrophy of a previously normal artery, and (3) persistence of the original single allantoid artery of the body stalk.11A number of genetic 12as well as environmental13-14 actors have been mentioned as possible causes of SUA. According to some authors15 SUA is etiologically heterogeneous, and more than one of the suggested mechanisms could be responsible. In our study we have seen that Out of 9870 all anomaly scan done in two years duration 80 were diagnosed as with Single Umbilical artery (SUA) so the prevalence of SUA in our study was 0.81% or 8.1 per one thousand anomaly scans done. The majority of the scans were with no any associated anomaly i.e. 67.5% followed by IUGR were 40%, Uro-genital were 16.25%, Cardiovascular were 15%, CNS were 11.25%, Skeletal were 8.75%, GIT were 6.25%. The anomalies like IUGR was 67.5 and 0.73%, Uro-genital -16.25 and 0.32, Cardiovascular -15% and 0.29%, CNS -11.25% and 0.20%, Skeletal- 8.75% and 0.17%, GIT-6.25% and 0.13% overall the presence of anomalies were significantly higher in SUA group as compared to Non SUA group (χ2 =1701, df=6, p<0.0001). These findings are similar to Meiling Hua 16they found Of 72,373 pregnancies, 64,047 (88.5%) had pregnancy follow-up information and were available for this analysis. There were 392 cases of single umbilical artery (0.61%) diagnosed at anatomic survey; slightly lower than previously reported. Single umbilical artery as compared with double umbilical artery was associated with increased risk of renal anomalies (adjusted odds ratio [OR] 3.0, 95% confidence interval [CI] 1.9 – 4.9, P<0.01 and cardiac anomalies (adjusted OR 20.3, 95% CI 13.5–30.4, P<0.01, suggest an increased risk of IUGR when the diagnosis of single umbilical artery is made, making a clinical recommendation for serial growth assessments in the setting of single umbilical artery reasonable.

 

CONCLUSION

It can be concluded from our study that the prevalence of SUA was 0.81%The majority of the scans were with no any associated anomaly i.e. 67.5% followed by IUGR were 40%, overall the presence of anomalies were significantly higher in SUA group as compared to Non SUA group.

REFERENCES

    • Doornebal N, de Vries TW, Bos AF, de Vries NK. Screening infants with an isolated single umbilical artery for renal anomalies: nonsense? Early Hum Dev 2007; 83:567–70.
    • Callen PW. Ultrasonography in obstetrics and gynecology. 4th ed. Philadelphia (PA): WB Saunders; 2000.
    • Budorick NE, Kelly TF, Dunn JA, Scioscia AL. The single umbilical artery in a high-risk patient population: what should be offered? J Ultrasound Med 2001; 20:619 –27; quiz 628.
    • Leung AK, Robson WL. Single umbilical artery: a report of 159 cases. Am J Dis Child 1989; 143:108 –10.
    • Neilson JP. Ultrasound for fetal assessment in early pregnancy (Cochrane Review). In: The Cochrane Library, Issue 2, Oxford Update Soft ware, 2000
    • Heifetz SA. Single umbilical artery: A statistical analysis of 237 autopsy cases and review of the literature. PerspectPediatrPathol 1984; 8:345-78.
    • Gornall AS, Kurinczuk JJ, Konje JC. Antenatal detection of a single umbilical artery: Does it matt er? PrenatDiagn 2003; 23:117-23.
    • Woo JS, Liang ST, Lo R. Characteristic patt ern of Doppler umbilical arterial velocity waveform in conjoint twins. GynecolObstet Invest 1987; 23:70-2.
    • Parilla BV, Tamura RK, MacGregor SN, Geibel LJ, Sabbagha RE. The clinical significance of a single umbilical artery as an isolated fi nding on prenatal ultrasound. ObstetGynecol 1995; 85:570-2.
    • Froehlich LA, Fujikura T. Follow-up of infants with single umbilical artery. Pediatrics 1973;52:6-13
    • Altshuler G, Tsang RC, Ermocilla R: Single umbilical artery. Correlation of clinical status and umbilical cord histology. Am J Dis Child 129:697, 1975
    • Geipel A, Germer U, Welp T, Schwinger E, Gembruch U. Prenataldiagnosis of single umbilical artery: determination of the absentside, associated anomalies, Doppler findings and perinatal outcome.Ultrasound ObstetGynecol 2000;15:114–117.
    • Kajii T, Shinohara M, Kikuchi K, Dohmen S, Akichika M.Thalidomide and the umbilical artery. Lancet 1963; 26:889.
    • Fiddler M, Pergament E. Is single umbilical artery a geneticallycontrolled anomaly? PrenatDiagn 1996; 16:969–971.
    • Martı´nez-Frı´as ML, Bermejo E, Rodrı´guez-Pinilla E, Prieto D;ECEMC Working Group. Does single umbilical artery (SUA) predict any type of congenital defect? Clinical-epidemiologicalanalysis of a large consecutive series of malformed infants.Am J Med Genet A 2008;146:15–25Ross JA, Jurkovic D, Zosmer N, et al. Umbilical cord cysts in early pregnancy. Obstet Gynecol. 1997; 89:442-5.
    • Meiling Hua, Anthony O. Odibo, MSCE, George A. Macones. Single Umbilical Artery and Its Associated Findings. The American College of Obstetricians and Gynecologists.2010;115(5) : 930-934