Skip to main content
Download PDF

Fetal heart rate evolution patterns in cerebral palsy associated with umbilical cord complications: a nationwide study

BMC Pregnancy and Childbirth volume 22, Article number: 177 (2022) Cite this article

Abstract

Background

The aim of the present study was to clarify fetal heart rate (FHR) evolution patterns in infants with cerebral palsy (CP) according to different types of umbilical cord complications.

Methods

This case–control study included children born: with a birth weight   ≥2000 g, at gestational age   ≥33 weeks, with disability due to CP, and between 2009 and 2014. Obstetric characteristics and FHR patterns were compared among patients with CP associated with (126 cases) and without (594 controls) umbilical cord complications.

Results

There were 32 umbilical cord prolapse cases and 94 cases with coexistent antenatal umbilical cord complications. Compared with the control group, the persistent non-reassuring pattern was more frequent in cases with coexistent antenatal umbilical cord complications (p = 0.012). A reassuring FHR pattern was observed on admission, but resulted in prolonged deceleration, especially during the first stage of labor, and was significantly identified in 69% of cases with umbilical cord prolapse and 35% of cases with antenatal cord complications, compared to 17% of control cases (p < 0.001).

Conclusion

Hypercoiled cord and abnormal placental umbilical cord insertion, may be associated with CP due to acute hypoxic-ischemic injury as well as sub-acute or chronic adverse events during pregnancy, while umbilical cord prolapse may be characterized by acute hypoxic-ischemic injury during delivery.

Peer Review reports

Background

Hypoxia–ischemia and acidemia are known causes of cerebral palsy (CP), although the etiology of many CP cases remains unknown [1]. Since placental and umbilical cord abnormalities are likely to induce a hypoxic fetal condition, an association between CP and these abnormalities has been previously reported [2, 3]. Our previous nationwide report [4] demonstrated that the major obstetric factors associated with CP after 33 weeks of gestation were placental abnormalities (31%) and umbilical cord abnormalities (15%).

Population-based studies have found that intrapartum hypoxia–ischemia is present in a smaller percentage of term children, with CP ranging from 8 to 28% in developed countries [1, 5, 6]; this rate has persisted over the past 30 years [1]. Therefore, CP may be associated with acute umbilical cord compression as well as chronic insufficient fetoplacental perfusion during the antepartum period. The pathology of umbilical cord abnormalities during labor might be associated with cord vulnerability to external forces during uterine contractions, resulting in acute hypoxia–ischemia (intrapartum hypoxia–ischemia). However, among the types of umbilical cord abnormalities, we hypothesized that an insufficiency in umbilical cord blood flow might vary from the antepartum period to delivery.

Classification of the fetal heart rate (FHR) evolution pattern in CP cases, as described by Phelan et al., is useful for determining the timing of asphyxial events that can cause fetal brain injury [7]. They analyzed intrapartum FHR in brain-damaged term infants, and divided them into the following groups: (1) bradycardia that indicates terminal fetal bradycardia on admission test, (2) a persistent non-reassuring pattern that continues from admission until delivery, (3) reassuring-prolonged deceleration that indicates reassuring admission tests followed by abrupt FHR changes with prolonged deceleration or bradycardia, (4) Hon’s pattern, described as a “stair-step to death” by Edward Hon in 1968, which indicates reassuring admission test findings and recurrent decelerations in FHR, high baseline FHR, and decreased variability followed by low baseline FHR, and (5) a persistent reassuring pattern throughout delivery.

Therefore, we hypothesized that the assessment of FHR evolution patterns would provide clues to the timing and preventability of injury in infants with CP associated with umbilical cord complications. In the present study, we aimed to clarify the FHR evolution patterns in patients with CP according to the different specific types of umbilical cord complications.

Methods

A case–control study was performed in children with CP who were approved for compensation by a review of the Japan Obstetric Compensation System for Cerebral Palsy (JOCSC). Disability was certified as first- or second-degree severity according to the grade of disability definitions in the Act on Welfare of Physically Disabled Persons.

Among the children born between January 2009 and July 2014, those with a birth weight ≥ 2000 g, gestational age ≥ 33 weeks, and disability due to CP independent of congenital causes or factors during the neonatal period or later, were included in the present study. Causations of CP associated with (cases) and without (controls) umbilical cord complications in each case were retrieved from reports of the Operating Organization of the JOCSC. Patients with undeterminable causes of CP were included as controls. Multiple pregnancies and FHR tracing that could not be evaluated (clear tracing missing from the medical records) were excluded from the present study.

JOCSC

Details of the JOCSC are described in our previous report [4]. The JOCSC was launched in January 2009 to provide prompt no-fault compensation for children diagnosed with CP caused by trauma during labor and delivery and for their respective families. The JOCSC covers more than 99% of delivery institutions throughout Japan. The JOCSC also provides information that could help in the prevention, early resolution of disputes, and improvement in the quality of obstetric healthcare. A review committee reviews the cases for compensation. After patients are declared as eligible to receive compensation by this review committee, their causes of CP are individually analyzed by the Causal Analysis Committee, which comprises obstetricians, pediatricians, midwives, and lawyers. Once collected, these individual cases are analyzed by the Recurrence Prevention Committee.

FHR analysis

The National Institute of Child Health and Human Development guidelines [8, 9] were applied when interpreting FHR patterns. We categorized the patients into five groups based on the FHR evolution patterns between admission and delivery, as modified by Phelan et al. [7]. The FHR evolution patterns were retrospectively analyzed by four authors (J.H., M.N., T.I., and E.J.) who were blinded to the clinical characteristics. FHR evolution patterns were determined after careful discussions. Cases with complete lack or partial lack of FHR strips (missing FHR tracing), those with different categorizations among investigators, and those with FHR patterns different from the below mentioned five included categories were excluded from the study.

Five groups based on FHR evolution patterns

When an abnormal FHR pattern was observed from the initial FHR examination on admission for delivery, the following two groups were defined: (i) The persistent non-reassuring group comprised fetuses with non-reassuring FHR, usually with decreased baseline variability on admission, and this pattern persisted until delivery. (ii) The persistent bradycardia group comprised fetuses with bradycardia or persistent severe decelerations with loss of variability from the beginning of FHR tracing on admission and no recovery until delivery.

In contrast, when a normal FHR pattern was observed on admission, the following three groups were defined: (iii) The Hon’s pattern group comprised fetuses with a normal FHR pattern on admission. Consequently, there were recurrent severe decelerations (especially variable deceleration) with or without increased baseline heart rate and decreased baseline variability. Finally, prolonged deceleration (PD) or bradycardia occurred before delivery. (iv) The reassuring-PD group comprised fetuses with a normal FHR pattern on admission; however, acute severe PD or bradycardia occurred before delivery. (v) The persistent reassuring group comprised fetuses with a normal FHR range during the entire course of delivery. (Table 1, Additional File 1).

Table 1 Definition of FHR patterns
Full size table

The umbilical cord complications analyzed in the present study included umbilical cord prolapse, marginal/velamentous cord insertion, multiple cord entanglement, a true knot, umbilical cord constriction, hypercoiled cord, hypocoiled cord, and umbilical cord with a single umbilical artery. The frequencies of FHR evolution patterns were compared between cases with CP associated with umbilical cord complications (cases) and cases with other causes (controls).

Umbilical cord complications

Findings of umbilical cord complications in the present study were based on macroscopic inspection of the medical records and/or microscopic investigation by obstetricians or midwives in each delivery institution. However, these definitions are usually used in each institution with reference to the Glossary of Obstetrics and Gynecology published by the Japan Society of Obstetrics and Gynecology [8]. Umbilical cord complications include umbilical cord prolapse in which the free loop of the normal umbilical cord accidentally prolapses into the vagina after rupture of the membrane and coexistent antenatal umbilical cord complications, which develop abnormally during pregnancy, such as the following conditions:

Velamentous and marginal cord insertion

Velamentous cord insertion is an abnormal cord insertion in which the umbilical vessels diverge as they traverse between the amnion and chorion before reaching the placenta. When the umbilical cord insertion is located just at the edge of the placenta without running through the membranous vessels, it is defined as a marginal cord insertion.

Multiple umbilical cord entanglement

Umbilical cord entanglement is the condition when one or more loops of the umbilical cord are encircled around any part of the fetus. In the present study, patients with two or more cord entanglements were included.

Umbilical cord constriction/narrow cord

Diagnosis of umbilical cord constriction is made by macroscopic evaluation when the umbilical cord has one or more narrow parts, including umbilical ring constriction, constriction in the free loop, and narrow umbilical cord without Wharton’s jelly.

True knot

True knot of the umbilical cord is formed when the fetus passes through a loop of the umbilical cord while being active in the uterus.

Abnormal umbilical coiling

The umbilical coiling index was calculated by dividing the total number of coils by the length of the cord in centimeters. Hypercoiled and hypocoiled cords after delivery are defined with umbilical coiling indices of ≥ 0.3 coils/cm (> 90% percentile) and < 0.1 coils/cm (< 10% percentile) [10].

Single umbilical artery

Diagnosis of a single umbilical artery is made macroscopically or microscopically when one umbilical artery is absent or obstructed.

Statistical analysis

A two-sided p-value of 0.05 was used to define statistical significance. All analyses were conducted using Stata version 13.0 (Stata Corporation, College Station, TX, USA). Continuous variables were reported as mean ± standard deviation and were compared using Student’s t-test or Mann–Whitney U-test. Integer variables were reported as medians and ranges and were compared using the Mann–Whitney U test. Categorical variables were reported as frequencies and compared using Fisher’s exact test.

Results

The flow diagram of the study is illustrated in Fig. 1. Among 1017 cases of CP from the JOCSC database, after the exclusion of 44 multiple pregnancies, 131 were considered to be associated with umbilical cord complications and 842 were considered to be caused by other reasons. After excluding cases with missing FHR and inability to classify FHR data, 126 cases of CP associated with umbilical cord complications and 594 controls with CP associated with other causes were finally analyzed for FHR evolution patterns.

Fig. 1
figure 1

Study flow diagram

Full size image

Characteristics of the patients with CP involving umbilical cord complications and other causes are summarized in Table 2, Additional file 2. Emergency cesarean section rate was significantly higher in patients with CP involving umbilical cord complications than in the controls (p < 0.001). Apgar scores in cases of CP involving umbilical cord complications were significantly lower than those in the controls (p < 0.001). The use of a cervical ripening balloon was associated with CP involving umbilical cord complications (p < 0.001).

Table 2 Major obvious obstetric factors considered as association with cerebral palsy
Full size table

The incidence of abnormal FHR evolution patterns in cases with cord prolapse, coexistent antenatal umbilical cord complications, and controls is depicted in Fig. 2. Of these, 32 had umbilical cord prolapse, and 94 had other coexistent antenatal umbilical cord complications. Abnormal FHR patterns had already been identified on admission (persistent non-reassuring and bradycardia) in 13% of cases with umbilical cord prolapse, 40% (35% + 5%) of cases with antenatal cord complications, and 37% (24% + 13%) of the controls. Compared with the control, the persistent non-reassuring pattern was more frequent in cases with antenatal cord complications (p = 0.012) and less frequent in cases with umbilical cord prolapse (p = 0.003). Reassuring FHR patterns were observed on admission, but abnormal FHR patterns during labor were more frequently observed in cases with cord complications than in controls. Reassuring-PD was significantly identified in 69% of cases with umbilical cord prolapse and 35% of cases with antenatal cord complications, compared to 17% of controls (p < 0.001). Continuation of reassuring FHR patterns until delivery was significantly less in cases with umbilical cord complications than in the control group.

Fig. 2
figure 2

Incidence of abnormal fetal heart rate evolution patterns in cases with cord prolapse, coexistent antenatal umbilical cord complications and control

Full size image

The timing and type of abnormal FHR evolution patterns stratified according to umbilical cord complications are summarized in Table 3. Abnormal FHR on admission was identified in various types of umbilical cord complications, especially hypercoiled cord (65%) and velamentous cord insertion (50%). In contrast, abnormal FHR patterns were likely to be observed during the first stage of labor in all types of umbilical cord complications, but abnormal FHR patterns during the second stage of labor were identified in 18% of multiple cord entanglements. During the first stage of labor, reassuring-PD was identified in cases of umbilical cord prolapse, cord constriction, hypocoiled cord, and cord with a single umbilical artery.

Table 3 Timing and type of abnormal fetal heart rate evolution patterns stratified by umbilical cord complications
Full size table

Discussion

While the FHR evolution pattern in cases with umbilical cord prolapse was characterized as reassuring-PD, FHR in cases with coexistent antenatal umbilical cord complications, such as hypercoiled cord and umbilical cord placental insertion site, were likely to be both persistent non-reassuring patterns on admission and reassuring-PD during the first stage of labor, compared to cases resulting in CP not associated with umbilical cord complications.

Regarding the timing of the hypoxic-ischemic injury, when the demonstration of an initially normal tracing was followed by patterns of hypoxia/ischemia, such as reassuring-PD and Hon’s patterns, it can be considered that CP was due to intrapartum hypoxic-ischemic injury. Reassuring-PD is considered an acute event causing hypoxic-ischemic damage during labor, while Hon’s pattern is considered a relatively sub-acute stress that affects the fetal brain, causing hypoxic-ischemic encephalopathy.

It is reasonable that the reassuring-PD pattern was identified in various types of umbilical cord complications, especially during the first stage of labor, because an abnormal FHR pattern and insufficient umbilical cord blood flow often originate from the vulnerability of the umbilical cord congenitally coexisting with the developing placenta. For example, in fetuses with velamentous cord insertion, abnormal FHR and perinatal complications are caused by a lack of Wharton’s jelly, which results in the compression of weak membranous vessels [11,12,13,14]. Hypercoiled cord could be more prone to cord torsion than to compression or stretching, which adversely affects blood flow during uterine contractions [15, 16]. Variable decelerations are more frequent, especially during the first stage of labor, in cases with a morphologically abnormal umbilical cord, such as velamentous cord insertion and hyper-coiled cord, than in cases without an abnormal umbilical cord [12, 13].

FHR monitoring of fetuses with coexistent antenatal umbilical cord complications often results in Hon’s pattern. We believe that the Hon’s pattern might be caused by the compressive and/or non-compressive failure of umbilical blood flow. Partial or progressive compression of the umbilical cord may lead to a Hon’s pattern. On the other hand, when previously normal tracing evolves slowly to severe abnormality through late or variable decelerations, this also suggests a mechanism of hypoxemic/acidemic basis for the injury, which may be related to a non-compressive failure of the umbilical blood flow. Structural umbilical cord abnormalities that develop during earlier gestation are likely to coexist with placental abnormalities [14, 17]. In such cases, insufficient fetoplacental perfusion during the progression of labor can induce abnormal FHR patterns, resulting in Hon’s pattern. In fact, Hon’s pattern was identified in all cases of velamentous insertion, which is often concomitant with abnormal placental growth.

In abnormal FHR evolution pattern on admission, persistent bradycardia was identified in cases with coexistent antenatal umbilical cord complications. According to us, these patients had already suffered acute or sub-acute compressive failure of umbilical blood flow before admission, resulting in bradycardia and traced FHR after admission.

Contrary to acute and sub-acute adverse events, persistent non-reassuring patterns indicate that causal events occurred over days or weeks before labor onset. In the present study, persistent non-reassuring patterns, such as absent or minimal baseline variability and bradycardia from the beginning of FHR tracing on admission, even before the onset of labor, were present in various types of coexistent antenatal umbilical cord complications. Without overt incriminating cord complications to explain a pre-existing abnormality of fetal tracing, one cannot be certain of the mechanism of preceding injury other than the notion that the timing was likely prepartum. A previous study demonstrated that umbilical cord abnormalities, which can obstruct umbilical cord blood flow, were significantly increased in neonates with placental fetal thrombocoagulopathy (FTV), who later developed CP [3]. According to a previous study, a potentially obstructive pathological umbilical cord, including decreased Wharton’s jelly, a narrow cord, and a hypercoiled cord, is also more frequent in neonates with FTV (30% vs. 9% in those without FTV) [3]. Our results support those of this previous study.

Concerning preventability, those with preexisting abnormal FHR patterns seem unlikely to be preventable (persistent non-reassuring and bradycardia). In addition, prevention of CP in cases with acute severe prolonged deceleration or continuous bradycardia may also be difficult. In a previous study in Japan that demonstrated the prognosis of infants with umbilical cord prolapse, the interval from the diagnosis of prolapse to delivery was found to be significantly longer in infants with a poor outcome than in infants with intact survival (median, 30 vs. 24 min.) [18]. Unless obstetric facilities throughout Japan can provide immediate cesarean section within 15 min, we will not be able to reduce the number of CP cases. Unfortunately, half of deliveries in Japan are managed in private clinics, which cannot perform emergency cesarean sections. However, we recommend initial FHR tracing and evaluation on admission to detect adverse effects related to the onset of labor or rupture of the membrane.

On the other hand, those with initial normal tracing and obvious later deterioration would be at least potentially preventable, especially those with Hon’s pattern. Previous studies have suggested that suboptimal intrapartum care could offer an obvious preventive opportunity for labor asphyxia, particularly in cases with normal admission FHR patterns [19, 20]. The combination of FHR monitoring with timely screening for maternal, obstetric, and fetal risk factors performed much better as a screening modality than FHR monitoring alone [21]. Furthermore, ultrasound screening for umbilical cord abnormalities, triage of pregnant women according to the risks of emergency cesarean section, and appropriate management of FHR and delivery are recommended [22, 23]. Pregnant women with umbilical cord abnormalities diagnosed by antenatal ultrasound should be placed under the continuous FHR observation while preparing for emergency cesarean section when contractions begin.

A limitation of the present study is that the assessment of umbilical cord complications might be slightly different among the different institutions because obstetricians or midwives evaluated umbilical cord abnormalities in their respective delivery institutions. Furthermore, since we only analyzed cases of CP in neonates with a birth weight of ≥ 2000 g and gestational age of ≥ 33 weeks as study subjects, we did not analyze the associations among CP, umbilical cord abnormalities, and fetal growth restrictions.

Conclusion

Our results suggest that umbilical cord complications that develop antenatally, such as hypercoiled cord and abnormal placental umbilical cord insertion, may be associated with CP due to acute hypoxic-ischemic injury as well as sub-acute or chronic adverse events during pregnancy, while umbilical cord prolapse may be characterized by acute hypoxic-ischemic injury during delivery.

Availability of data and materials

The datasets generated and/or analyzed during the current study are not publicly available. The JOCSC data were obtained with cooperation from birthing facilities and families. Therefore, it is necessary for this organization to handle personal information with great care, and thus, our policy does not provide outside access to these data. An article in the Standard Conditions of the Japan Obstetric Compensation System stipulates that access to the personal information of children who develop cerebral palsy and their families, as well as of the birthing facilities, is strictly limited to the staff of the JCQHC.

Abbreviations

CP:

Cerebral palsy

FHR:

Fetal heart rate

JOCSC:

Japan Obstetric Compensation System for Cerebral Palsy

FTV:

Fetal thrombocoagulopathy

PD:

Prolonged deceleration

P-Brady:

Persistent bradycardia

P-NR:

Persistent non-reassuring

R-PD:

Reassuring-prolonged deceleration

References

  1. Graham EM, Ruis KA, Hartman AL, Northington FJ, Fox HE. A systematic review of the role of intrapartum hypoxia-ischemia in the causation of neonatal encephalopathy. Am J Obstet Gynecol. 2008;199(6):587–95.

    Article  CAS  Google Scholar 

  2. Nakamura M, Umehara N, Ishii K, Sasahara J, Kiyoshi K, Ozawa K, Tanaka K, Tanemoto T, Ichizuka K, Hasegawa J, et al. A poor long-term neurological prognosis is associated with abnormal cord insertion in severe growth-restricted fetuses. J Perinat Med. 2018;46(9):1040–7.

    Article  Google Scholar 

  3. Redline RW. Clinical and pathological umbilical cord abnormalities in fetal thrombotic vasculopathy. Hum Pathol. 2004;35(12):1494–8.

    Article  CAS  Google Scholar 

  4. Hasegawa J, Toyokawa S, Ikenoue T, Asano Y, Satoh S, Ikeda T, Ichizuka K, Tamiya N, Nakai A, Fujimori K, et al. Relevant obstetric factors for cerebral palsy: from the nationwide obstetric compensation system in Japan. PLOS ONE. 2016;11(1):e0148122.

    Article  Google Scholar 

  5. Blair E, Stanley FJ. Intrapartum asphyxia: a rare cause of cerebral palsy. J Pediatr. 1988;112(4):515–9.

    Article  CAS  Google Scholar 

  6. Hagberg B, Hagberg G, Beckung E, Uvebrant P. Changing panorama of cerebral palsy in Sweden VIII Prevalence and origin in the birth year period 1991–94. Acta paediatrica. 2001;90(3):271–7.

    Article  CAS  Google Scholar 

  7. Phelan JP, Ahn MO. Fetal heart rate observations in 300 term brain-damaged infants. Journal of maternal-fetal investigation: the official journal of French society of ultrasound in medicine and biology [et al]. 1998;8(1):1–5.

    CAS  Google Scholar 

  8. Macones GA, Hankins GD, Spong CY, Hauth J, Moore T. The 2008 National Institute of Child Health and Human Development workshop report on electronic fetal monitoring: update on definitions, interpretation, and research guidelines. Obstet Gynecol. 2008;112(3):661–6.

    Article  Google Scholar 

  9. Electronic fetal heart rate monitoring: research guidelines for interpretation. National Institute of Child Health and Human Development Research Planning Workshop. National Institute of Child Health and Human Development Research Planning Workshop. Am J Obstet Gynecol. 1997;177(6):1385–90.

    Article  Google Scholar 

  10. Strong TH Jr, Jarles DL, Vega JS, Feldman DB. The umbilical coiling index. Am J Obstet Gynecol. 1994;170(1 Pt 1):29–32.

    Article  Google Scholar 

  11. Hasegawa J, Matsuoka R, Ichizuka K, Sekizawa A, Okai T. Ultrasound diagnosis and management of umbilical cord abnormalities. Taiwan J Obstet Gynecol. 2009;48(1):23–7.

    Article  Google Scholar 

  12. Hasegawa J, Matsuoka R, Ichizuka K, Nakamura M, Sekizawa A, Okai T. Do fetal heart rate deceleration patterns during labor differ between various umbilical cord abnormalities? J Perinat Med. 2009;37(3):276–80.

    Article  Google Scholar 

  13. Hasegawa J, Matsuoka R, Ichizuka K, Kotani M, Nakamura M, Mikoshiba T, Sekizawa A, Okai T. Atypical variable deceleration in the first stage of labor is a characteristic fetal heart-rate pattern for velamentous cord insertion and hypercoiled cord. J Obstet Gynaecol Res. 2009;35(1):35–9.

    Article  Google Scholar 

  14. Hasegawa J, Matsuoka R, Ichizuka K, Sekizawa A, Farina A, Okai T. Velamentous cord insertion into the lower third of the uterus is associated with intrapartum fetal heart rate abnormalities. Ultrasound Obstet Gynecol. 2006;27(4):425–9.

    Article  CAS  Google Scholar 

  15. Predanic M, Perni SC, Chervenak FA. Antenatal umbilical coiling index and Doppler flow characteristics. Ultrasound Obstet Gynecol. 2006;28(5):699–703.

    Article  CAS  Google Scholar 

  16. Georgiou HM, Rice GE, Walker SP, Wein P, Gude NM, Permezel M. The effect of vascular coiling on venous perfusion during experimental umbilical cord encirclement. Am J Obstet Gynecol. 2001;184(4):673–8.

    Article  CAS  Google Scholar 

  17. Hasegawa J, Matsuoka R, Ichizuka K, Otsuki K, Sekizawa A, Farina A, Okai T. Cord insertion into the lower third of the uterus in the first trimester is associated with placental and umbilical cord abnormalities. Ultrasound Obstet Gynecol. 2006;28(2):183–6.

    Article  CAS  Google Scholar 

  18. Hasegawa J, Sekizawa A, Ikeda T, Koresawa M, Ishiwata I, Kawabata M, Kinoshita K. Japan Association of Obstetricians and Gynecologists: Clinical risk factors for poor neonatal outcomes in umbilical cord prolapse. Journal of maternal-fetal and neonatal medicine. 2016;29(10):1652–6.

    Article  Google Scholar 

  19. Jonsson M, Agren J, Nordén-Lindeberg S, Ohlin A, Hanson U. Suboptimal care and metabolic acidemia is associated with neonatal encephalopathy but not with neonatal seizures alone: a population-based clinical audit. Acta Obstet Gynecol Scand. 2014;93(5):477–82.

    Article  CAS  Google Scholar 

  20. Jonsson M, Ågren J, Nordén-Lindeberg S, Ohlin A, Hanson U. Neonatal encephalopathy and the association to asphyxia in labor. Am J Obstet Gynecol. 2014;211(6):667.e1-667.e8.

    Article  Google Scholar 

  21. Eden RD, Evans MI, Evans SM, Schifrin BS. The “fetal reserve index”: re-engineering the interpretation and responses to fetal heart rate patterns. Fetal Diagn Ther. 2018;43(2):90–104.

    Article  Google Scholar 

  22. Takita H, Hasegawa J, Arakaki T, Nakamura M, Tokunaka M, Oba T, Sekizawa A. Antenatal ultrasound screening using check list before delivery for predicting a non-reassuring fetal status during labor. Journal of maternal-fetal and neonatal medicine. 2018;31(1):1–6.

    Article  Google Scholar 

  23. Hasegawa J. Ultrasound screening of umbilical cord abnormalities and delivery management. Placenta. 2018;62:66–78.

    Article  Google Scholar 

Download references

Acknowledgements

We thank members of the Recurrence Prevention Committee, Japan Obstetric Compensation System for Cerebral Palsy, Public Interest Incorporated Foundation, Japan Council for Quality Health Care, for their excellent support in data collection and organization.

Funding

None.

Author information

Authors and Affiliations

  1. Visiting Researcher, Department of the Japan Obstetric Compensation System for Cerebral Palsy in Public Interest Incorporated Foundation, Japan Council for Quality Health Care, Tokyo, Japan

    Junichi Hasegawa, Masahiro Nakao & Satoshi Toyokawa

  2. Department of Obstetrics and Gynecology, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki, Kanagawa, 216-8511, Japan

    Junichi Hasegawa

  3. Department of Obstetrics and Gynecology, Mie University Graduate School of Medicine, Mie, Japan

    Masahiro Nakao & Tomoaki Ikeda

  4. Department of Obstetrics and Gynecology, Sakakibara Heart Institute, Tokyo, Japan

    Masahiro Nakao

  5. The Prevention Recurrence Committee, Japan Obstetric Compensation System for Cerebral Palsy, Tokyo, Japan

    Tomoaki Ikeda, Shoji Satoh, Kiyotake Ichizuka, Nanako Tamiya, Akihito Nakai, Keiya Fujimori, Tsugio Maeda, Satoru Takeda, Mitsutoshi Iwashita & Tsuyomu Ikenoue

  6. Department of Public Health, The University of Tokyo, Tokyo, Japan

    Satoshi Toyokawa

  7. Department of the Japan Obstetric Compensation System for Cerebral Palsy, Japan Council for Quality Health Care, Tokyo, Japan

    Emi Jojima, Hideaki Suzuki & Shigeru Ueda

  8. Maternal and Perinatal Care Center, Oita Prefectural Hospital, Oita, Japan

    Shoji Satoh

  9. Department of Obstetrics and Gynecology, Showa University Northern Yokohama Hospital, Kanagawa, Japan

    Kiyotake Ichizuka

  10. Department of Health Services Research, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan

    Nanako Tamiya

  11. Department of Obstetrics and Gynecology, Nippon Medical School, Tokyo, Japan

    Akihito Nakai

  12. Department of Obstetrics and Gynecology, Fukushima Medical University, Fukushima, Japan

    Keiya Fujimori

  13. Maeda Clinic, Incorporated Association Anzu-kai, Shizuoka, Japan

    Tsugio Maeda

  14. Department of Obstetrics and Gynecology, Juntendo University Faculty of Medicine, Tokyo, Japan

    Satoru Takeda

  15. Kugayama Hospital, Tokyo, Japan

    Mitsutoshi Iwashita

  16. Miyazaki University, Miyazaki, Japan

    Tsuyomu Ikenoue

Authors
  1. Junichi Hasegawa
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Masahiro Nakao
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Tomoaki Ikeda
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Satoshi Toyokawa
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Emi Jojima
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Shoji Satoh
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Kiyotake Ichizuka
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Nanako Tamiya
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Akihito Nakai
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Keiya Fujimori
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Tsugio Maeda
    View author publications

    You can also search for this author in PubMed Google Scholar

  12. Satoru Takeda
    View author publications

    You can also search for this author in PubMed Google Scholar

  13. Hideaki Suzuki
    View author publications

    You can also search for this author in PubMed Google Scholar

  14. Shigeru Ueda
    View author publications

    You can also search for this author in PubMed Google Scholar

  15. Mitsutoshi Iwashita
    View author publications

    You can also search for this author in PubMed Google Scholar

  16. Tsuyomu Ikenoue
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

JH, NM, TI, and TI conceived of the study. JH wrote the initial protocol, analyzed the data, and wrote the first draft of the manuscript. All authors collected data and analyzed the cases of CP. JH, MN, TI, and EJ coordinated the study, and JH, MN, TI, and EJ produced the database. ST and NT performed the statistical analyses. All authors contributed to the writing of the manuscript. TI, SS, KI, ST, AN, KF, TM, ST, HS, SU, and TI were the guarantors for this study. All authors had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. The lead author affirms that this manuscript is an honest, accurate, and transparent account of the study being reported, that no important aspects of the study have been omitted, and that any discrepancies from the study as planned have been explained. The author(s) read and approved the final manuscript.

Corresponding author

Correspondence to Junichi Hasegawa.

Ethics declarations

Ethics approval and consent to participate

All procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study protocol was approved by the institutional review boards (IRBs) of the Operating Organization of the Japan Obstetric Compensation System for Cerebral Palsy (JOCSC; No.26–01, Aug. 5th, 2014). Since the waiver for informed consent was provided by the IRB, written informed consent was not obtained from the patients. However, patients were provided with the announcement of the implementation of a “case–control study for cerebral palsy and prevention of its recurrence.” (Additional file 3) Although the analysis was retrospective, data for the anonymized JOCSC database were collected in a normal clinical setting and the confidentiality of the patients involved was protected. All patient records and information were anonymized and de-identified before the analysis.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hasegawa, J., Nakao, M., Ikeda, T. et al. Fetal heart rate evolution patterns in cerebral palsy associated with umbilical cord complications: a nationwide study. BMC Pregnancy Childbirth 22, 177 (2022). https://doi.org/10.1186/s12884-022-04508-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12884-022-04508-2

BMC Pregnancy and Childbirth

ISSN: 1471-2393

Contact us