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DOI: 10.1055/a-1722-2721
M-Sign in Middle Cerebral Artery Doppler Waveforms: A Sign of Fetal Vasoconstriction Before and After Open Fetal Spina Bifida Repair
M-Zeichen in der Arteria cerebri media Dopplerwelle: ein Hinweis auf fetale Vasokonstriktion vor und nach offener fetaler Spina Bifida OperationAbstract
Background Increased pulse wave reflection in the fetal arterial system, illustrated by a second systolic peak (M-sign) in middle cerebral artery (MCA) Doppler waveforms, allows interpretation of fetal systemic vasoconstriction. Little is known about fetal vascular regulation during fetal spina bifida (fSB) repair. Therefore, the aim of this study was to analyze MCA-Doppler waveform changes before, during, and after fSB repair. Patients and Methods 31 pregnant women who underwent fSB repair were included. Fetal MCA-Doppler waveforms were prospectively analyzed before, during and after fSB repair, and categorized as follows: normal systolic downslope, systolic shoulder, second systolic peak (M-sign), and concave systolic downslope. These MCA waveforms were related to maternal and fetal characteristics, to anesthetic medication, and to umbilical artery (UA) waveforms. Results Before fSB repair, all fetuses repeatedly presented M-signs. After initiation of desflurane for general anesthesia, systolic shoulder and the M-sign vanished in 24/31 (78%) fetuses and 19/31 (61%) showed transient UA ARED flow. A significant association between these two Doppler findings was found (p=0.007). After fSB repair, signs of increased pulse wave reflection reappeared but resolved over time (23 days ± 20, SD) in all fetuses. Conclusion Both fSB and intrauterine repair influence fetal vascular regulation. This phenomenon can be illustrated by MCA-Doppler waveforms. While anesthetic agents transiently eliminated M-signs and often provoked a UA ARED flow, fSB repair finally led to normalization of MCA-Doppler waveforms indicating return to normal fetal vascular regulation.
Zusammenfassung
Hintergrund Eine erhöhte Pulswellenreflektion im fetalen Kreislauf, im Sinne erhöhter Vasoaktivität, spiegelt sich in einem zweiten systolischen Ausschlag (M-Zeichen) der A. cerebri media (ACM) wider. Bisher ist kaum etwas über die fetale Kreislaufregulation während der fötalen Spina Bifida (fSB) Operation bekannt. Daher war das Ziel dieser Studie, die Änderungen im ACM-Dopplerwellenmuster vor, während und nach fSB-Operationen zu analysieren. Methodik 31 konsekutiv für fSB operierte Feten wurden eingeschlossen. ACM-Doppler wurden prospektiv vor, während und nach der fSB-Operation analysiert und wie folgt kategorisiert: normal, systolische Schulter, M-Zeichen, konkaves Muster. Die Wellenmuster wurden mit maternalen und fetalen Charakteristika sowie mit Narkosemitteln und dem A. umbilicalis-(UA)-Muster korreliert. Resultate Alle Feten zeigten M-Zeichen vor der fSB-Operation. Nach Beginn der Vollnarkose mit Desfluran verschwanden die Zeichen der Vasokonstriktion in 24/31 (78%) – und 19/31 (61%) der Feten zeigten einen Block oder Rückfluss in der UA. Der Zusammenhang zwischen beiden Dopplerbefunden war signifikant (p=0,007). Zeichen erhöhter Pulswellenreflektion sind nach der fSB-Operation initial wieder erschienen, über die Zeit (23 Tage ± 20, SD) jedoch bei allen Feten verschwunden. Schlussfolgerung Die fSB-Läsion und eine fetale Operation beeinflussen den fetalen Kreislauf. Dieses Phänomen lässt sich gut mittels ACM-Doppler illustrieren. Während die Narkosemittel das M-Zeichen passager verschwinden lassen und oft ein pathologisches UA-Muster provozieren, resultiert die fSB-Operation letztlich in einer Normalisierung des ACM-Dopplermusters bzw. des fetalen Kreislaufes.
Publication History
Received: 24 June 2021
Accepted after revision: 10 December 2021
Article published online:
08 February 2022
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References
- 1 Adzick NS, Thom EA, Spong CY. et al. A randomized trial of prenatal versus postnatal repair of myelomeningocele. N Engl J Med 2011; 364 (11) 993-1004
- 2 Mohrlen U, Ochsenbein-Kolble N, Mazzone L. et al. Benchmarking against the MOMS Trial: Zurich Results of Open Fetal Surgery for Spina Bifida. Fetal Diagn Ther 2020; 47 (02) 91-97
- 3 Moehrlen U, Ochsenbein N, Vonzun L. et al. Fetal surgery for spina bifida in Zurich: results from 150 cases. Pediatr Surg Int 2021; 37 (03) 311-316
- 4 Vonzun L, Kahr MK, Noll F. et al. Systematic classification of maternal and fetal intervention-related complications following open fetal myelomeningocele repair – results from a large prospective cohort. BJOG 2020;
- 5 Winder FM, Vonzun L, Meuli M. et al. Maternal Complications following Open Fetal Myelomeningocele Repair at the Zurich Center for Fetal Diagnosis and Therapy. Fetal Diagn Ther 2019; 46 (03) 153-158
- 6 Rychik J, Tian Z, Cohen MS. et al. Acute cardiovascular effects of fetal surgery in the human. Circulation 2004; 110 (12) 1549-1556
- 7 Kassir E, Belfort MA, Shamshirsaz AA. et al. Doppler changes in umbilical artery and ductus venosus during fetoscopic prenatal surgical repair of myelomeningocele. Ultrasound Obstet Gynecol 2019; 53 (03) 335-339
- 8 Sinskey JL, Rollins MD, Whitlock E. et al. Incidence and Management of Umbilical Artery Flow Abnormalities during Open Fetal Surgery. Fetal Diagn Ther 2018; 43 (04) 274-283
- 9 Gonser M, Tavares de Sousa M, Klee A. et al. OC02: Second systolic peak in middle cerebral artery Doppler of fetuses with severe anemia: an explanatory model based on fetal pulse wave reflection. Ultrasound Obstet Gynecol 2018; 52 (04) 555
- 10 Gonser M, Pavelan N, Gharib M. Optimisation criterion for pulsatile timing: observation in the human fetus. Ultrsound Obst Gynecol 2020; 56 (Suppl. 01) 197-198
- 11 Gonser M, Klee A. et al. A systolic shoulder in fetal middle cerebral artery Doppler wavefroms may indicate fetal pulse wave reflection and transmission to cerebral circulation – a contribution to fetal circulatory physiology. Ultraschall in Med 2018; 39: S1-S47
- 12 Gonser M, Tavares M, Ochsenbein-Koelble N. et al. Fetal pulse wave and pulsatile timing assessement in MCA-doppler of fetuses with severe anemia and after IUT. Ultrasound Obstet Gynecol 2020; 56 (Suppl. 01) 135-136
- 13 Moehrlen U, Elrod J, Ochsenbein-Kolble N. et al. In utero Hepatitis B Immunization during Fetal Surgery for Spina Bifida. Fetal Diagn Ther 2019; 1-4
- 14 Vonzun L, Winder FM, Meuli M. et al. Prenatal Sonographic Head Circumference and Cerebral Ventricle Width Measurements Before and After Open Fetal Myelomeningocele Repair – Prediction of Shunting During the First Year of Life. Ultraschall in Med 2018;
- 15 Mazzone L, Moehrlen U, Casanova B. et al. Open Spina Bifida: Why Not Fetal Surgery?. Fetal Diagn Ther 2019; 45 (06) 430-434
- 16 Meuli M, Meuli-Simmen C, Mazzone L. et al. In utero Plastic Surgery in Zurich: Successful Use of Distally Pedicled Random Pattern Transposition Flaps for Definitive Skin Closure during Open Fetal Spina Bifida Repair. Fetal Diagn Ther 2017;
- 17 Ochsenbein-Kolble N, Krahenmann F, Husler M. et al. Tocolysis for in utero Surgery: Atosiban Performs Distinctly Better than Magnesium Sulfate. Fetal Diagn Ther 2018; 44 (01) 59-64
- 18 Varsos GV, Czosnyka M, Smielewski P. et al. Cerebral critical closing pressure in hydrocephalus patients undertaking infusion tests. Neurol Res 2015; 37 (08) 674-682
- 19 Mulder EJ, de Heus R, Visser GH. Antenatal corticosteroid therapy: short-term effects on fetal behaviour and haemodynamics. Semin Fetal Neonatal Med 2009; 14 (03) 151-156
- 20 Kahler C, Schleussner E, Moller A. et al. Doppler measurements in fetoplacental vessels after maternal betamethasone administration. Fetal Diagn Ther 2004; 19 (01) 52-57
- 21 Bachman CR, Biehl DR, Sitar D. et al. Isoflurane potency and cardiovascular effects during short exposures in the foetal lamb. Can Anaesth Soc J 1986; 33 (01) 41-47
- 22 Adamson SL, Langille BL. Factors determining aortic and umbilical blood flow pulsatility in fetal sheep. Ultrasound Med Biol 1992; 18 (03) 255-266
- 23 Reuwer PJHM, Nuyen WC, Beijer HJM. et al. Fetoplacental Circulatory Competence. Eur J Obstet Gyn R B 1986; 21 (01) 15-26
- 24 Thompson RS, Stevens RJ. Mathematical model for interpretation of Doppler velocity waveform indices. Med Biol Eng Comput 1989; 27 (03) 269-276
- 25 Thompson RS, Trudinger BJ. Doppler waveform pulsatility index and resistance, pressure and flow in the umbilical placental circulation: an investigation using a mathematical model. Ultrasound Med Biol 1990; 16 (05) 449-58
- 26 Biehl DR, Yarnell R, Wade JG. et al. The uptake of isoflurane by the foetal lamb in utero: effect on regional blood flow. Can Anaesth Soc J 1983; 30 (06) 581-516
- 27 Palahniuk RJ, Shnider SM. Maternal and fetal cardiovascular and acid-base changes during halothane and isoflurane anesthesia in the pregnant ewe. Anesthesiology 1974; 41 (05) 462-472
- 28 Vonzun L, Winder FM, Meuli M. et al. Hindbrain Herniation and Banana and Lemon Sign After Open Fetal Myelomeningocele Repair – When Do These Signs Disappear and is Shunting Predictable. Ultraschall in Med 2020;