Placental vascular anastomoses are extremely rare in dichorionic twins, but almost ubiquitous in monochorionic twins. These vascular anastomoses allow antenatal inter-twin blood transfusion and may lead to severe complications such as twin–twin transfusion syndrome (TTTS) or twin anemia–polycythemia sequence (TAPS). However, in most monochorionic twins, inter-twin blood transfusion between the two fetuses is ‘balanced’ and the pregnancy evolves without complications until birth. During birth, acute shifts of blood through the vascular anastomoses may also occur and lead to large Hb differences between the two neonates (Lopriore et al., 2005; Reference Lopriore, Holtkamp, Sueters, Middeldorp, Walther and Oepkes2014). A few small studies in uncomplicated monochorionic twins reported significantly higher Hb levels in second-born twins compared to first-borns, suggesting a possible role for intrapartum placento-fetal transfusion (Faxelius et al., Reference Faxelius, Raye, Gutberlet, Swanstrom, Tsiantos, Dolanski and Stahlman1977; Klebe & Ingomar, Reference Klebe and Ingomar1972; Lopriore et al., 2005). However, these studies are limited by small sample sizes, hampering the interpretation of the results and the evaluation of possible risk factors.
The aim of this study was to evaluate the Hb differences at birth in a large cohort of uncomplicated monochorionic twins and determine the effect of birth order, mode of delivery, and time-interval to delivery between twin 1 and twin 2.
Methods
All consecutive monochorionic twins delivered at our tertiary care center between May 2002 and October 2015 were included in this retrospective study. We excluded monochorionic twins affected by TTTS, TAPS, twin reversed arterial perfusion sequence (TRAP) or single or double fetal demise. Similarly, when the first twin was delivered vaginally and the co-twin through secondary CS, the twin pair was also excluded. We defined TTTS according to the Eurofoetus criteria, with a cut-off at a deepest vertical pocket of amniotic fluid in the donor at ≤2 cm and in the recipient of ≥8 cm within the first 20 weeks of gestation or ≥10 cm after gestational week 20 (Senat et al., Reference Senat, Deprest, Boulvain, Paupe, Winer and Ville2004). The definition of TAPS was based on the presence of inter-twin Hb difference >8 g/dL and at least one of the following criteria: reticulocyte count ratio >1.7 or placenta injection with colored dye showing only minuscule anastomoses (diameter <1 mm; Slaghekke et al., Reference Slaghekke, Kist, Oepkes, Pasman, Middeldorp, Klumper and Lopriore2010).
Hb levels were routinely assessed at birth from umbilical cord blood or venous blood directly from the neonate when umbilical cord blood could not be used. Since Hb levels are subject to significant change in the first few hours after birth, and in particular in cases with acute large shifts due to intra-partum blood transfusion, we also recorded Hb levels on day 2 (Lopriore et al., 2005). The following perinatal data was collected: gestational age at birth, mode of delivery (CS or vaginal delivery), and time interval between delivery of the first twin and the second twin (in minutes). We were not able to record the timing of cord clamping as this is not routinely registered in deliveries occurring at our center. Local guidelines recommend cord clamping at 60–90 s, but this varies in practice.
The following neonatal data were collected: gender, birth weight, birth weight discordance, occurrence of polycythemia, treatment with partial exchange transfusion or red blood cell transfusion in the first 2 days of life, and neonatal mortality. Birth weight discordance was calculated by dividing the difference in birth weight between twins by the birth weight of the larger twin. Polycythemia was defined as a venous hematocrit level >65%. Neonatal mortality was defined as death within 28 days after birth. Acute peripartum TTTS was defined as an Hb difference of at least 8 g/dL at birth, without signs of TAPS or chronic TTTS (Lopriore et al., Reference Lopriore, Holtkamp, Sueters, Middeldorp, Walther and Oepkes2014). In case of polycythemia, partial exchange transfusion was performed when venous hematocrit >70% in asymptomatic patients or hematocrit >65% in symptomatic patients (Rosenkrantz, Reference Rosenkrantz2003).
The primary outcome of the study was inter-twin Hb differences at birth and day 2. Data were analyzed in association with birth order, mode of delivery, and time interval between delivery of twin 1 and twin 2.
The hospital's Research Ethics Committee approved the study (protocol number: P15.325).
Statistics
Data are reported as means and standard deviations (SD) or as medians and interquartile ranges (IQR), as appropriate. Continuous values within twin pairs were analyzed using the paired t test. Paired nominal data were analyzed using the McNemar test. Unpaired continuous data were analyzed using the Mann–Whitney Test. For comparing unpaired nominal data, the chi-square test was used. The Spearman correlation coefficient was used to study the relationship between time interval at birth between the first-born twin and the second-born twin and Hb levels. A p value <.05 was considered to be statistically significant. SPSS version 20 was used for performing the analysis (SPSS, Inc., Chicago, Illinois, USA).
Results
A total of 290 monochorionic twin pairs were analyzed in this retrospective study, including 171 (59%) twin pairs delivered vaginally and 119 (41%) pairs born through CS. Baseline characteristics of the population are shown in Table 1.
aValue given as mean ± SD or median (IQR).
At birth, paired Hb samples were available in 143 (84%) twin pairs in the vaginal delivery group and 115 (97%) twin pairs in the CS group. On day 2, paired Hb samples were available in 89 (52%) vaginally born twin pairs and 67 (56%) in the CS group. Hb levels in relation to birth order and mode of delivery are presented in Table 2. Mean Hb levels at birth were significantly higher in second-born twins when delivered vaginally, but no differences were detected between twin 1 and 2 when delivered through CS. Inter-twin Hb differences were significantly larger in twins delivered vaginally compared to CS, 1.9 (IQR: 0.6–3.9) g/dL versus 1.1 (IQR: 0.4–3.1) g/dL (p = .02).
aValue given as mean ± SD or median (IQR); bHb levels at birth were available in 143 twin pairs delivered vaginally and in 115 twin pairs delivered through CS. cHb levels on day 2 were available in 91 twin pairs delivered vaginally and in 64 twin pairs delivered through CS. Hb = hemoglobin, CS = cesarean section.
On day 2, inter-twin Hb differences increased and became more evident in twins born vaginally. Second-born twins had a higher Hb level in 70% (100/143) of cases at birth and 80% (74/93) on day 2 after vaginal birth. In the CS group, second-born twins had a higher Hb level in 62% (70/113) of cases at birth and 54% (35/65) of cases on day 2.
The median time interval between the birth of twin 1 and twin 2 by means of vaginal delivery was 9 (IQR: 5–16) minutes. The median delivery time interval in the twins born through CS was 2 (IQR: 1–2) minutes. In both groups, no association between prolonged inter-twin delivery time interval and Hb level differences were found. We found no association between delivery time interval and Hb levels at birth or day 2 in second-born twins after vaginal delivery, as shown in Figure 1.
The rate of polycythemia was significantly higher in second-born twins compared to first-borns after vaginally delivery, 12% (20/166) versus 1% (2/166) (p < .01). No difference was detected in the CS group, 1% (1/119) versus 0% (0/199; p = .99).
Acute peripartum TTTS (Hb difference >8 g/dL at birth) occurred in 5.2% pregnancies (9/166) and was detected only in twin pairs after vaginal delivery. Second-born twins were always the recipient twins in case of acute peripartum TTTS. Further details on the clinical characteristics are listed in Table 3.
aIn first two days after birth. CS = cesarean section.
Discussion
This study showed that Hb differences at birth are a common finding in monochorionic twins born vaginally, even in the absence of TTTS or TAPS. We found that Hb differences are only present after vaginal delivery but not after CS, highlighting an important effect of mode of delivery. In addition, Hb levels are usually higher in second-born twins suggesting an important role of birth order. Our data suggest that inter-twin blood shifts may occur during vaginal delivery particularly towards the second twin.
Our findings confirm observations from a few small studies (Faxelius et al., Reference Faxelius, Raye, Gutberlet, Swanstrom, Tsiantos, Dolanski and Stahlman1977; Galea et al., Reference Galea, Scott and Goel1982; Klebe & Ingomar, Reference Klebe and Ingomar1972; Lopriore et al., 2005), although they differ from the findings of Bhide et al. (Reference Bhide, Prefumo, Sairam, Cobian-Sanchez and Thilaganathan2006). While they found a trend towards a lower Hb level in a group of 20 second-born monochorionic twins, the small sample size may have hampered their conclusions (Bhide et al., Reference Bhide, Prefumo, Sairam, Cobian-Sanchez and Thilaganathan2006). In a previous, similar study from our research group, we found no association between mode of delivery and Hb differences (Lopriore et al., 2005). Again, the small study groups (28 twin pairs delivered vaginally and 17 pairs delivered through CS) prevented accurate statistical analyses. The large sample size in our present study reduces the risks of bias and may allow unraveling of the complex mechanisms that regulate inter-twin blood shifts during delivery. The other important strength of this study is that we were able to collect data for Hb levels at birth as well as on day 2. In general, Hb levels in neonates (whether singletons or twins) increase in the first few hours after birth. The initial short-term increase is due to hemoconcentration as plasma moves towards the extravascular space to compensate for the placental transfusion and increase in circulating red cell volume at the time of delivery. After several hours, Hb levels in neonates gradually decreases (Brans et al., Reference Brans, Shannon and Ramamurthy1981; Gairdner et al., Reference Gairdner, Marks, Roscoe and Brettell1958). In addition, in case of acute shifts of blood, initial Hb level measurements are known to be unreliable. When acute blood loss occurs, Hb levels initially remain stable due to vasoconstriction (Drucker et al., Reference Drucker, Chadwick and Gann1981). Hb levels reflecting the true blood loss can only be clearly detected after several hours, due to a compensatory mechanism of equilibration termed hemodilution. Hemodilution is a gradual increase in intravascular volume and plasma volume that takes place to compensate for acute blood loss (Saito et al., Reference Saito, Shimazu, Miyamoto, Maemura and Satake2013). Conversely, when an infant receives an acute transfusion of blood, the expected rise in Hb levels is only seen after several hours once equilibration between the intravascular and extravascular spaces is achieved. This is why we chose in this study to record Hb levels at birth as well as on day 2.
Inter-twin Hb differences in monochorionic twins are known to be mediated through the invariable presence of placental vascular anastomoses connecting the two fetal circulations. Inter-twin Hb differences may already be present during pregnancy and can be associated with several disorders such as TAPS or TTTS. Inter-twin Hb differences may also occur during delivery in uncomplicated monochorionic twins. The exact pathophysiologic mechanism leading to inter-twin blood transfusion during delivery is not well known. Some authors suggested that uterine contractions or changes in fetal positioning may lead to inter-twin blood pressure differences and exacerbated inter-twin blood transfusion through the vascular anastomoses (Lehndorff, Reference Lehndorff1961; Sherer et al., Reference Sherer, Sinkin, Metlay and Woods1992; Wenstrom et al., Reference Wenstrom, Tessen, Zlatnik and Sipes1992). However, evidence for this hypothesis is lacking. Various other alternatives may explain the inter-twin Hb differences. In this study, we found a similar decrease in Hb levels (0.3–0.4 g/dL) between birth and day 2 in both first- and second-born twins delivered through CS. In contrast, in twins born vaginally, the decrease in Hb level in first-born twins is more prominent (1.3 g/dL) and is associated with a concomitant increase in Hb levels in second-born twins. The increase in Hb levels in second-born twins suggests that twin 2 may receive more blood during vaginal delivery. One hypothesis is that this increase in Hb level in twin 2 may result from blood transfusion from twin 1 to twin 2 during delivery (which could explain the significant decrease in Hb level in twin 1). Alternatively, the increase in Hb level in twin 2 may result from transfusion of blood from both placental shares into the circulation of the second twin (placento-fetal transfusion) through the patent vascular anastomoses (Lopriore & Oepkes, Reference Lopriore and Oepkes2008; Lopriore et al., 2005). A third hypothesis is that the increase in Hb levels in second-born twins could be related to the time interval between delivery of twin 1 and twin 2. Theoretically, prolonged time interval until delivery of twin 2 could be associated with increased placento-fetal transfusion towards twin 2 and explain the higher Hb levels in second born twins. However, our data do not support this theory since we found no association between prolonged delivery time interval and Hb levels in twin 2. Last, a fourth hypothesis is that the large Hb differences between twin 1 and twin 2 could be related to the timing of cord clamping. As shown in various studies, Hb levels at birth are strongly related with the timing of cord clamping. Late cord clamping (>30 s after birth) leads to higher Hb levels due to increased placento-fetal transfusion compared to early cord clamping (McDonald et al., Reference McDonald, Middleton, Dowswell and Morris2013; Mercer, Reference Mercer2001; Rabe et al., Reference Rabe, Diaz-Rossello, Duley and Dowswell2012). Unfortunately, the timing of cord clamping was not recorded at our center and may vary between caregivers. Although it is tempting to assume that the time taken to clamp each cord was not different during delivery of each twin pair, it is possible that a difference could have occurred. Obstetricians may theoretically be tempted to clamp the cord of the first-born twin more quickly to focus their attention towards the sometimes more complicated delivery of the second twin. The significant drop in Hb level in twin 1 may be the result of relatively very early cord clamping resulting in reduced placento-fetal transfusion towards twin 1.
Although our study was not designed to assess the impact of timing of cord clamping, our data may have implications concerning the timing of cord clamping. Since second-born twins delivered vaginally have increased Hb levels and are more often at risk of polycythemia, delayed cord clamping may not be advisable in second-born twins. In contrast, since first-born twins have a significant decrease in Hb levels, early cord clamping should be avoided in first-born twins. Evidently, these suggestions must be tested in appropriately designed studies to evaluate the benefits of different cord-clamping strategies in this particular subgroup of monochorionic twins delivered vaginally.
Although our study is the largest study so far to analyze Hb levels in uncomplicated monochorionic twins, care should be taken when interpreting due to the retrospective nature of the study. Another limitation of our study is that Hb levels on day 2 were only measured in 53% of the included neonates and that timing of cord clamping was not recorded. Both findings are inherent to the retrospective nature of the study and should be taken into account when designing a prospective study in the future.
In conclusion, twins born second generally have higher Hb levels at birth and on day 2 when delivered vaginally, but no inter-twin Hb differences were detected after CS. Whether Hb differences result primarily from increase in Hb levels in twin 2 due to placento-fetal transfusion, decrease in Hb levels in twin 1 due to early cord clamping, or inter-twin blood shifts from twin 1 to twin 2 during delivery is not clear. Targeted studies to evaluate the optimal timing of cord clamping in monochorionic twins delivered vaginally are obviously required. Further studies are also necessary to determine the association between Hb differences in monochorionic twins and the number, type, and size of placental vascular anastomoses. These studies may improve our understanding of the pathophysiological mechanisms leading to blood shifts in monochorionic twins at birth.