Monochorionic Twins: Ultrasound Monitoring Schedule According to ISUOG 2025
What Changes with Monochorionicity
Monochorionic twins are not just two pregnancies in one uterus, but a single placental hemodynamic system with vascular anastomoses. Therefore, the standard monitoring interval for dichorionic twins is insufficient here: complications can develop between scheduled screenings. In the updated document ISUOG 2025 Updated Practice Guidelines: role of ultrasound in twin pregnancy, the basic principle is formulated practically: first, accurately determine chorionicity, then manage the monochorionic pregnancy with a biweekly ultrasound schedule for early detection of TTTS, TAPS, and selective growth restriction.
Start: Determine Chorionicity Before 14 Weeks
The optimal window for determining chorionicity is 11+0–13+6 weeks. The physician should document the number of gestational sacs, amnions, placental masses, the thickness of the intertwin membrane, and ultrasound signs at its attachment to the placenta. The lambda sign is typical for dichorionicity, while the T-sign is indicative of monochorionicity. If chorionicity is unclear after the first trimester, it is safer to manage the pregnancy as monochorionic until proven otherwise, as the cost of missing TTTS or TAPS is higher than the cost of more frequent monitoring.
Basic Ultrasound Monitoring Schedule for MCDA
For uncomplicated monochorionic diamniotic twins, ISUOG recommends starting specialized ultrasound monitoring at 16 weeks and repeating it every 2 weeks. This interval is primarily chosen for the early detection of twin-to-twin transfusion syndrome, which usually manifests in the second trimester and requires rapid referral to a fetal therapy center.
| Gestational Age | Action | Objective |
|---|---|---|
| 11+0–13+6 weeks | Confirm viability, date the pregnancy, determine chorionicity and amnionicity | Establish the correct monitoring pathway |
| From 16 weeks | Ultrasound every 2 weeks | Screening for TTTS and early signs of discordant development |
| Around 18–22 weeks | Detailed anatomy of each fetus; cardiac assessment at the center's level of expertise | Exclusion of structural anomalies, more common in twins |
| From 20 weeks | Growth, amniotic fluid, Doppler; for monochorionic twins — MCA-PSV assessment for TAPS | Detection of IUGR, TAPS, and hemodynamic decompensation |
| Until delivery | Continue biweekly visits, more frequently if complications arise | Do not miss rapid changes in the condition of one or both fetuses |
Minimum Protocol for Each Visit
In the report, it is advisable to separately describe fetus A and fetus B, using a consistent method of identification: position, side of the uterus, relation to the internal os, gender if possible, placental and umbilical cord features. At each biweekly visit for MCDA, assess the heartbeats of both fetuses, the maximum vertical pocket of amniotic fluid in each amnion, bladder filling, biometry and estimated weight, growth discordance, and Doppler indices according to the clinical situation. For TAPS screening after 20 weeks, the peak systolic velocity in the middle cerebral artery of both fetuses is crucial.
Key ISUOG Thresholds for Practice
| Situation | Ultrasound Criterion | Practical Significance |
|---|---|---|
| TTTS: oligohydramnios in donor | DVP <2 cm | One of the mandatory signs of the syndrome |
| TTTS: polyhydramnios in recipient | DVP ≥8 cm before 20 weeks; DVP ≥10 cm after 20 weeks | In combination with DVP <2 cm in the other fetus, requires urgent expert evaluation |
| Weight discordance | ≥25% | Marker of high risk of adverse outcome and reason for increased monitoring |
| Discordance calculation | (EFW larger − EFW smaller) / EFW larger × 100% | The formula should be consistent in all reports |
| Antenatal TAPS | MCA-PSV in donor >1.5 MoM and in recipient <1.0 MoM; alternatively, intertwin difference in MCA-PSV >0.5 MoM | Suspicion of chronic intertwin transfusion without the typical poly-/oligohydramnios sequence |
TTTS: How Not to Miss It
Twin-to-twin transfusion syndrome in MCDA is diagnosed not by size difference, but by a combination of pronounced amniotic fluid imbalance: one fetus with DVP <2 cm, the other with polyhydramnios according to gestational threshold. Additionally, assess the donor's bladder, Doppler abnormalities, hydrops, and fetal viability. These signs correspond to Quintero's clinical staging: from stage I with a visible donor bladder to stage V with the death of one or both fetuses. If TTTS is suspected at gestational ages potentially suitable for fetoscopic laser coagulation of anastomoses, the report should directly recommend urgent referral to a fetal medicine center.
Selective Growth Restriction: What to Include in the Report
In monochorionic twins, selective IUGR is associated not only with placental insufficiency but also with unequal placental territory distribution and anastomoses. ISUOG uses EFW discordance ≥25% as an important risk threshold. The protocol should specify the centile of EFW and abdominal circumference of each fetus, the degree of discordance, fluid volume, and Doppler. For monochorionic selective IUGR, classification by blood flow in the umbilical artery of the smaller fetus is crucial: type I — positive end-diastolic flow, type II — persistently absent or reversed, type III — intermittently absent or reversed. Types II and III require expert monitoring due to a higher risk of sudden deterioration.
TAPS: Why MCA-PSV is Needed
Twin anemia-polycythemia sequence can occur spontaneously or after TTTS treatment. Unlike TTTS, TAPS may not have the classic polyhydramnios/oligohydramnios pair, so a single DVP measurement is insufficient. Screening is based on comparing MCA-PSV in both fetuses: increased in the presumed anemic fetus and decreased in the polycythemic fetus. Threshold criteria are MCA-PSV >1.5 MoM in the donor and <1.0 MoM in the recipient or an intertwin difference >0.5 MoM. It is important to report MoM, not just absolute velocity, as the indicator depends on gestational age.
Monochorionic Monoamniotic Twins
MCMA is a separate high-risk group. There is no intertwin membrane here, so TTTS criteria based on separate amniotic pockets are not applicable, but the risk of cord entanglement and sudden events is higher. Ultrasound should confirm the absence of a membrane, exclude conjoined twins, assess anatomy, growth, and Doppler of each fetus. The frequency of monitoring and timing of delivery are determined by a center experienced in managing MCMA; however, ISUOG principles remain the same: early accurate diagnosis of amnionicity, regular monitoring of both fetuses, and a low threshold for referral to a specialized center.
Practical Referral Template
The ultrasound diagnostician should not only describe the findings but also indicate the risk. The wording can be brief: MCDA, gestational age, both fetuses alive, DVP right/left, bladders visualized or not, EFW and discordance, UA/MCA-PSV as indicated, no signs of TTTS/TAPS or suspicion present. If DVP <2 cm in one fetus and polyhydramnios in the other, MCA-PSV pattern of TAPS, EFW discordance ≥25%, pathological blood flow in the umbilical artery of the smaller fetus, or the death of one fetus, the report should conclude with a recommendation for urgent consultation with a fetal medicine specialist.
Frequently asked questions
From what gestational age should ultrasounds be performed every 2 weeks for MCDA?
From 16 weeks. Before this, it is important to determine chorionicity at 11+0–13+6 weeks and correctly route the pregnancy.
What are the minimum TTTS signs to look for at each visit?
The maximum vertical pocket in each amnion and the bladders of both fetuses. Diagnostically significant is the combination of DVP <2 cm in one fetus and polyhydramnios in the other.
When should MCA-PSV be added for monochorionic twins?
From 20 weeks for TAPS screening, especially after laser treatment of TTTS or in cases of unexplained discordance in fetal condition.