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Addressing Patient-Provider Communication Gaps in Vanishing Twin Syndrome: Implications for Patient Care and Clinical Guidelines

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06 June 2025

Posted:

09 June 2025

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Abstract
Introduction: Vanishing twin syndrome (VTS) refers to the in utero demise of one or more fetuses in a multiple pregnancy, often with physical remains persisting throughout gestation or at birth. Despite increased detection via early ultrasound and due to the use of ART, clinical protocols for VTS remain inadequate. This systematic review assesses physical and psychological risks, the current state of patient-provider communication, and international guideline gaps in VTS care. Materials & Methods: A systematic literature review was conducted using key search terms including but not limited to “vanishing twin* syndrome,” “patient-provider communicat*,” and “bereave* care.” Studies were selected based on relevance to patient experiences, international clinical guidelines, and the physical and psychological impacts of vanishing twin syndrome. Results: Patients with vanishing twin syndrome report inconsistent disclosure, inadequate emotional support, and confusion regarding the management of fetal remains. Physical risks to surviving multiples include low birth weight, placental pathology, and neurodevelopmental concerns. Maternal serum screening and cfDNA results are often confounded due to lingering fetal DNA or hormones from the demised fetus(es). These complications are underreported and poorly explained in current research and clinical guidances. Conclusions: Improved vanishing twin syndrome management requires early chorionicity assessment, updated screening protocols, and training on compassionate disclosure. Evidence-based guidelines should account for screening artifacts, placental sequelae, and bereavement care. Future studies must stratify outcomes by gestational age at loss, chorionicity, and ART exposure to clarify risks and optimize care.
Keywords: 
vanishing twin syndrome
;  
patient-provider communication
;  
bereavement support
;  
clinical information
;  
multiple pregnancies
;  
twin pregnancies
;  
fetal loss
;  
miscarriage
Subject: 
Public Health and Healthcare  -   Other
Vanishing twin syndrome (VTS) refers to the phenomenon where a twin or multiple gestation pregnancy is diagnosed via ultrasound, but one or more embryos or fetuses cease to develop during any trimester in gestation (Zamani & Parekh, 2021). However, this definition is controversial, as some researchers define VTS exclusively as a first-trimester event (Landy et al., 1982), whereas others acknowledge that fetal losses meeting similar clinical criteria may also occur later in gestation (Zamani & Parekh, 2021). The literature has also presented the term “vanishing twins syndrome” (where twins is plural) and consequently solely analyzed twin pregnancies where both sacs or embryos disappeared (Sun et al., 2017). In both terms, complete vanishment may be implied misleadingly, and the plural version may further imply falsely that more than one twin vanishes. Batsry and Yinon (2022) implied VTS is exclusively applicable to twin pregnancies and not higher-order multiples, reflecting another layer of complexity with the term. VTS may result in one of the following outcomes, which vary by the stage of development at the time of loss, cause of death, and type of multiples:
1.
Complete Resorption
  • This outcome typically occurs in the first trimester, after embryonic development, when a fetus forms and then demises in utero. The deceased fetus may be completely or partially resorbed into the pregnant individual and/or the surviving co-twin(s). Biological materials such as fetal cells, RNA/DNA, proteins, and hormones may enter the maternal circulation and/or integrate into the co-twin(s) (Zamani & Parekh, 2021). These losses occur slightly later than those involving a blighted ovum.
2.
Retention of Remnants
In some cases, fetal or gestational remnants persist throughout pregnancy and, similar to cases of full resorption, biological material may enter the maternal circulation and/or integrate into the co-twin(s) (Zamani & Parekh, 2021). This includes:
    • Blighted ovum (anembryonic pregnancy): A gestational sac forms without an embryo. Diagnosed typically at 6–7 weeks, it often resorbs by the end of the first trimester but can persist throughout pregnancy in some cases (Chaudhry et al., 2023; Davies et al., 2016; Zamani & Parekh, 2021).
    • Residual embryonic, fetal, and placental remains: Tissues from a demised conceptus may remain visible on ultrasound or at birth and may contribute to cell-free DNA or protein in the maternal bloodstream throughout gestation (Zamani & Parekh, 2021).
3.
Fusion or Integration (Including Mummification)
  • Later gestational losses may result in more complex integration of fetal tissue. For example, fetus papyraceous, which is a rare but severe form of VTS where the deceased fetus becomes mummified and compressed against the uterine wall or membranes. This typically occurs in the second or third trimester and is almost always visible at birth. It poses significant risks to the pregnant individual and surviving multiples (Zamani & Parekh, 2021).
The vanishing twin phenomenon was first described in the medical literature in the 1940s by a German obstetrician, Walter Stoeckel, who noted that the rate of multiple pregnancies was far greater than that of their births (Stoeckel, 1945). However, the term “vanishing twin syndrome” was not first coined until Landy et al. (1982) presented it in a literature review. Since that time, VTS has become more widely recognized due to advancements in ultrasound technology (Zamani & Parekh, 2021). Twinning rates, and subsequent rates of VTS, have increased both with increasing use of assisted reproductive technologies (ART) (i.e., due to multiple embryo transfer or hyperovulation) and due to rising maternal age, yet research on VTS has lagged due to historical underdiagnosis of VTS (Sun et al., 2017; Zamani & Parekh, 2021). The absence of significant literature on the subject has led to inconsistent patient-provider communication, inadequate standardized care protocols, and significant emotional distress for affected families. This systematic review synthesizes existing research on VTS, including its impact on the current state of patient-provider communication, interpretation of prenatal screening results, fetal development, maternal health, and the challenges in standardizing medical protocols.
  • Inadequate Diagnosis of VTS
While some individuals with VTS could be diagnosed postpartum (e.g., fetus papyraceous), VTS patients as a population were, by technological and diagnostic limitations, underrecognized before ultrasound was used widely in obstetric and gynecological medicine in the 1970s-1980s in most developed nations (Abramowicz, 2021; Johnson & Carter, 2017). VTS is frequently underreported, particularly in naturally conceived pregnancies, as most cases “vanish” (i.e., resorb) completely within the first trimester—often before a patient’s first prenatal appointment, which typically occurs between 8 and 13 weeks gestation (Zamani & Parekh, 2021). Even when prenatal care begins early, cases of VTS may still go unrecorded due to inadequate diagnostic terminology and limited provider awareness of the syndrome. For instance, rather than diagnosing a patient with VTS, a provider may instead classify the event as a “blighted ovum,” leading to further misclassification and misunderstanding of VTS’s clinical implications. VTS also serves as a biological and clinical confounder in fetal development research, with evidence suggesting that male VTS survivors may carry biological vulnerabilities that impact infant survival rates (Catalano et al., 2025). This finding suggested that VTS has been an overlooked factor in studies linking fetal size to infant mortality, and suggests that selection against frail male twins in utero may partially explain fluctuations in neonatal mortality rates.
  • Literature Search Strategies
This systematic literature review aims to assess clinical and psychosocial gaps in the diagnosis, management, and communication of VTS. Specifically, the review addresses the following research questions:
  • What are the physical and psychological risks associated with VTS for mothers and surviving multiples?
  • How do healthcare providers communicate with patients regarding VTS, and what barriers exist to effective communication?
  • How do international clinical guidelines vary in their treatment of VTS, and what opportunities exist for global harmonization or improvement?
To explore these questions, we conducted a systematic literature review using key search terms such as "vanishing twin syndrome," "patient-provider communicat*," and "bereave* care." Studies were selected based on their relevance to patient experiences, international clinical guidance, and reported physical and psychological outcomes associated with VTS.*
  • Care, Communication, and Protocols: Emotional Impacts and Physical Risks
In addition to challenges with the terminology used to describe the type of fetal loss, providers often struggle with how to communicate fetal loss effectively in both singleton and multiple pregnancies throughout gestation as well as at birth, leaving patients uninformed and unsupported (Brann et al., 2021; Rankin et al., 2021). Hayton (2010) suggested that many providers may opt not to inform their VTS patients that they have experienced a loss. This article noted that poor communication regarding VTS is often not intentional or done out of malice. Rather, the ways in which experienced physicians define and value life may impact what providers deem medically necessary to inform patients about—especially when at least one healthy embryo remains intact and/or when the loss occurs early on (e.g., before the detection of a viable heartbeat). However, withholding such information may lead to confusion or emotional distress. Parents who remain unaware of a loss may struggle to make sense of their own physical or emotional symptoms, such as unexplained grief, hormonal shifts, or abnormal screening results, thereby increasing anxiety. In contrast, several studies have demonstrated that patients who are better informed tend to experience lower levels of stress and anxiety, likely due to a clearer understanding of their circumstances and care options (Bolejko & Hagell, 2021; Fischbeck et al., 2021). Legg et al. (2015) further indicated that well-informed patients tend to harbor more hope—often in the form of optimism for the healthy development of the surviving twin and confidence in their ability to cope with the pregnancy ahead.
Swanson et al. (2002) found that bereaved mothers of multiples generally reported significantly higher scores on the Perinatal Grief Scale compared to bereaved mothers of singletons, attributing this difference partially to the lack of recognition and validation from others. An additional complication identified by Cubbage (2023) and Morgan (2002) arises from inconsistencies across institutions, states, and countries regarding the classification and management of fetal remains versus medical waste. In the United States, federal regulations define a fetus as "the product of conception from implantation until delivery," with "delivery" meaning complete separation of the fetus from the pregnant individual (45 CFR § 46.202, 2024). Additionally, a "dead fetus" is federally defined as one exhibiting no heartbeat, spontaneous respiratory activity, voluntary muscle movement, or umbilical cord pulsation (45 CFR § 46.202, 2024). However, national and state level laws vary widely concerning handling, testing, and memorialization requirements for fetal remains. For example, Indiana enacted legislation (HEA 1337) requiring that fetal remains from abortions be either buried or cremated, treating them similarly to human remains (Cromer & Bjork-James, 2023). In contrast, New York State law requires a burial permit and disposition of fetal remains only if the spontaneous abortion occurs after 20 weeks of gestation. Prior to this gestational age, there is no legal requirement for the mother to be informed or involved in the disposal process (Nahidi et al., 2021). This approach allows medical facilities to handle fetal remains from earlier gestational losses as medical waste, without imposing additional obligations on healthcare providers or patients. Considering the international complexities, Middlemiss (2021) noted significant inconsistencies in the governance and terminology surrounding fetal remains in England, illustrating tensions between viewing them as pregnancy remains, infant remains, or human corpses. Furthermore, hospitals affiliated with distinct religious traditions (e.g., Catholic versus Adventist) often follow differing ethical guidelines when defining "life," potentially further complicating decisions about disposal or memorialization of fetal tissues. This complexity is especially pronounced in cases of partial fetal resorption associated with VTS, where fetal remains may still be physically attached to the placenta of the surviving multiple(s).
The clinical and developmental outcomes associated with VTS vary in their level of empirical support, with some complications well-established and others remaining controversial or poorly understood. Among the most consistent findings are placental pathologies—including velamentous cord insertion, abnormal placental morphology, and placental weights below the 10th percentile—which are reported across multiple studies and are particularly associated with monochorionic pregnancies (Evron et al., 2015; Batsry & Yinon, 2022). Conversely, associations between VTS and congenital anomalies, such as spina bifida or other fetal malformations, are largely based on limited case reports rather than robust cohort studies. Nevertheless, some studies have reported an increased prevalence of congenital anomalies, including spina bifida and other malformations, in surviving twins following early loss of a conceptus (Pharoah et al., 2009; Shinnick et al., 2017). Additionally, the risk of cerebral palsy has been found to be higher among surviving twins after the intrauterine demise of a co-twin, further suggesting potential developmental vulnerabilities associated with VTS (Pharoah et al., 2002). Reports of fetal malformations such as conjoined twins or partial resorption anomalies remain biologically plausible in early gestation but are rare and difficult to quantify due to limitations in detection and documentation.
Among fetal outcomes, survivors of VTS may be at increased risk for low birth weight and low Apgar scores; however, these findings are difficult to disentangle from baseline risks associated with multifetal gestations, particularly in the context of preterm birth or late gestational loss (Ahmed et al., 2016; Roberts & Toth, 2020; Seong et al., 2020). Other reported complications, such as intrauterine growth restriction (IUGR), gestational diabetes, placental abruption, placental sequelae (e.g., infarcts, hematomas, or fibrosis in the region where the fetus was lost), cervical insufficiency, chronic hypertension, and premature rupture of membranes (PROM), are inconsistently reported and often confounded by chorionicity, timing of loss, or use of ART (Evron et al., 2015; Khalil et al., 2025; Li et al., 2023; Seong et al., 2020). In cases of VTS with a blighted ovum or a vanished multiple with residual membranes where fetal remains fuse with the surviving co-twin(s), their placenta, or persist throughout gestation, there may be a diversion of resources that may elicit risks depicted in Table 1, including but not limited to neurodevelopmental impairment and fetal growth restriction (Nerlich et al., 1992; Park et al., 2012). Vaginal bleeding, while commonly observed in some VTS cases, is a nonspecific symptom that frequently occurs in early pregnancy and may be linked to a variety of unrelated causes, such as implantation, subchorionic hematoma, or early miscarriage. Although some studies report increased rates of bleeding in VTS, it is unclear whether this is a VTS-specific risk or reflective of broader multifetal or ART-related vulnerabilities (Seong et al., 2020; Evron et al., 2015). Therefore, its association with VTS remains controversial and requires further controlled investigation.
Psychologically, mothers experiencing VTS may suffer prolonged emotional distress from the time of loss through the postpartum period, underscoring the need for trauma-informed counseling and emotional support (Cubbage et al., 2025; Harris et al., 2020; Highet et al., 2022; Roberts & Toth, 2020; Weitzner et al., 2023). Similarly, surviving offspring—particularly monozygotic twins—have been linked to increased risk of mood disorders and other emotional or behavioral challenges, although the evidence remains mixed due to variations in methodology and control for confounding variables (Song et al., 2020; Batsry & Yinon, 2022).
Emerging research also highlights that VTS may act as a biological confounder in fetal development Epigenetic (e.g., changes in methylation and histone regulation) consequences of VTS have been proposed and warrant further investigation as they may impact gene expression in the surviving twin. (Császár & Bókkon, 2019; Fjeldstad et al., 2020; Yu et al., 2002). However, these outcomes are likely underreported due to the need for advanced or long-term testing, which is not routinely performed. Epigenetic changes following the loss of a multiple(s) can be considered pathological when they disrupt normal gene expression patterns in the surviving multiple(s), potentially affecting neurodevelopment, stress regulation, or long-term health. Such changes may have multigenerational implications. Moreover, changes may be triggered by intrauterine stress, vascular events, or the absorption of cellular material from the demised twin. As shown in Table 1, future research should aim to distinguish VTS-specific outcomes from those associated with general twin pregnancies while prioritizing long-term follow-up and stratification by gestational timing, chorionicity, and ART exposure.
  • Well-established across studies: Findings consistently reported across multiple, high-quality studies with replication in different populations.
  • Inconsistent results across studies: Evidence varies between studies, likely influenced by sample size, study design, chorionicity, gestational timing of loss, or confounding factors.
  • Rare, likely underreported: Observed primarily in isolated case reports or small cohorts; lacks systematic investigation.
     
  • Theoretical/emerging evidence: Proposed based on biological plausibility, case studies, or preliminary data; not yet validated through large-scale empirical studies.
Although rare, chimerism may result from multiple pregnancies (Monden et al., 2021). It typically arises from the fusion of two genetically distinct zygotes or the resorption of deceased fetal material into a co-developing fetus, processes that are more likely in dizygotic twin gestations. Thus, the likelihood and impact of chimerism vary with chorionicity—being more plausible in dichorionic pregnancies—and, to a lesser extent, amnionicity and gestational timing (Zamani & Parekh, 2021). In contrast, monozygotic twins in monochorionic or monoamniotic configurations share nearly identical genetic material, making chimerism extremely rare in such cases. Chimerism may occasionally be detected during genetic testing, such as chromosomal microarray (CMA) with SNP probes or genome sequencing, though many cases go unnoticed. Most findings are incidental and clinically insignificant unless an abnormal cell line is involved. However, chimerism can affect histocompatibility and genetic testing interpretation and, in rare instances, has resulted in parentage discrepancies due to tissue-specific genetic variation (Yu et al., 2002). Beyond chimerism, fraternal dichorionic/diamniotic (DCDA) twins often present the lowest risks for adverse outcomes compared to multiples that share the same sac and/or placenta (Patrick et al., 2022; Shinnick et al., 2017). This therefore highlights the need for both providers and patients to be better informed about fetal loss and the specific characteristics of multiple types (e.g., chorionicity and amnionicity).
While VTS and conditions such as teratomas, parasitic twins, and fetus-in-fetu are typically understood as distinct entities, some researchers have hypothesized embryologic overlap. Rare case reports suggest that remnants of a resorbed twin in early gestation might contribute to the development of complex masses, including teratomas or malformed parasitic structures (Dhingra et al., 2008; Freire Gameiro et al., 2024). Although teratomas are most often attributed to pluripotent germ cell anomalies, more speculative theories point to early twinning errors or the incorporation of embryonic tissue during resorption as possible contributing factors (Spencer, 2001; McDonald et al., 2020). Fetus in fetu, often considered a severe form of parasitic twinning, has also been proposed to overlap histologically with teratomas due to similar tissue composition and imaging characteristics (Feizi et al., 2020). However, these connections remain theoretical, with most reports lacking molecular evidence of a preceding twin demise. Moreover, if such developmental disruptions occur pre-implantation, they would fall outside the diagnostic scope of VTS, which requires post-implantation evidence of a vanished co-twin (Zamani & Parekh, 2021). Thus, while biologically plausible, a causal link between clinically recognized VTS and parasitic outcomes remains unproven and should be interpreted with caution.
VTS and other types of multiple loss may impact screening results, including maternal serum screening (MSS). MSS measures hormones and proteins (e.g., hCG, PAPP-A, AFP) in maternal blood, which may be abnormally elevated or suppressed due to the presence or loss of a second fetus. In VTS cases, particularly following early loss, trophoblastic tissue from the demised embryo may remain metabolically active, producing hormones like hCG and sustaining limited vascular activity. This residual trophoblastic activity can result in persistently abnormal serum marker levels. Choe et al. (2021) reported that while PAPP-A and AFP levels tend to normalize over time, hCG and inhibin A may remain elevated for more than four weeks after fetal demise, complicating the interpretation of first- and second-trimester screening results. Although nuchal translucency (NT) itself may not be directly altered, its interpretation in conjunction with these serum markers can yield inaccurate risk estimates. For this reason, MSS is generally not recommended in pregnancies affected by VTS due to the high likelihood of false-positive or false-negative results (Choe et al., 2021). Lee et al. (2023) conducted a multicenter prospective cohort study and found that pregnancies complicated by a vanishing twin had significantly altered first- and second-trimester maternal serum marker levels compared to singleton pregnancies, including elevated hCG and inhibin A and decreased PAPP-A, further supporting concerns regarding the interpretation of MSS results in the context of VTS.
Identification of VTS is also critical for interpreting the results of cfDNA screening for the ongoing pregnancy. 50% of all early pregnancy losses may result from chromosomal abnormalities (Essers et al., 2023), and DNA from a demised co-twin may continue to be detected in cfDNA for up to 15 weeks after the loss (Raymond et al., 2024). Therefore, vanishing twins are a common source of false positives in prenatal cfDNA screening (Batsry & Yinon, 2022; van Eekhout et al., 2023). It is recommended that positive prenatal cfDNA screening results be confirmed by diagnostic testing, which involves a cytogenetic assessment of DNA collected from chorionic villus sampling (CVS) or an amniocentesis. Given that VTS impacts the accuracy of cfDNA screening, a history of VTS for the ongoing pregnancy warrants additional discussion with a genetic counselor regarding the likelihood of a true positive upon diagnostic testing. VTS must also be considered when the pregnant individual receives a low-risk prenatal cfDNA result, as other discrepancies can occur, including an incorrect sex call (Bianchi & Chiu, 2018).Prenatal cfDNA screening results may represent the status of the ongoing pregnancy, the co-twin demise, the placenta, a maternal condition, a combination of these factors, or a false positive. As a result, this screening assay cannot diagnose the genetic status of the pregnancy loss. This information may be important for the health of the pregnant individual. For example, some partial hyatidiform moles (PHM; resulting from the fertilization of a normal egg by two or more sperm) and complete hyatidiform moles (CHM; resulting from the fertilization of an a nuclear egg by one or two sperm) cause gestational trophoblastic disease, which rarely for PHM and more frequently for CHM can develop into gestational trophoblastic neoplasia (Gonzalez et al., 2024; Lindor et al., 1992). In these cases, serial testing of human chorionic gonadotropin (HCG) levels after removal of molar tissue from the uterus is important to monitor for risks of transforming into a malignant condition (Gonzalez et al., 2024).
Genetic diagnostic testing of the loss may also be desired for a psychological benefit to parents and to identify if there is a significant risk of recurrence for a given genetic abnormality in future pregnancies (Schilit et al., 2022). Diagnostic testing can be performed on products of conception (POC) after delivery of the ongoing pregnancy, which can often be identified by examination of the placenta by a pathologist. Referral to a genetic counselor is warranted given the complexity of this testing. For example, cytogenetic assessment of the tissue should involve CMA and not karyotype, which requires successful tissue culture from fresh living tissue that would not be available for older deceased remains. If information about triploidy is desired (for example, diandric triploidy, which results in PHM), a CMA should include SNP probes. Results should be interpreted with caution, as they may be confounded by maternal cell contamination and/or the surviving co-twin.
  • Challenges in Establishing Guidelines for VTS
Establishing guidelines that serve pregnancies where there is a loss of one or more fetuses can be challenging, as they would ideally necessitate the involvement of professionals who comprise the complex system of care coordination (Weitzner et al., 2023). For example, guidelines may include the need for nuanced interpretation of serum and prenatal cell-free DNA screening results, as well as patient options or resources for fetal remains disposal or diagnostic genetic testing, memorialization, bereavement, and counseling. This lack of information is likely to be due in part to poor translation of evidence of research from the bench to bedside for both providers and institutions (Abu-Odah et al., 2022). Establishing comprehensive guidelines for pregnancies affected by VTS involves addressing several complex challenges, such as the following:​
  • Underdiagnosis and Limited Literature: VTS is often underdiagnosed, especially in naturally conceived pregnancies, leading to a scarcity of comprehensive studies and literature on the condition. This lack of data hampers the development of evidence-based guidelines.​
  • Perceived Importance by Providers: As previously cited, some healthcare providers may not fully recognize the physical and emotional significance of VTS depicted in Table 1, resulting in inconsistent management approaches and a lack of standardized care protocols.​
  • Composition and Availability of Care Teams: Effective management of VTS requires a multidisciplinary team, including obstetricians, genetic counselors, mental health professionals, and bereavement counselors. However, access to such professionals is not uniform across regions. For instance, the Southern United States has a notably low number of genetic counselors, averaging 0.69 per 100,000 residents, with many concentrated in urban areas. This disparity limits access for patients in rural communities (Villegas & Haga, 2019).​
  • Insurance Coverage and Financial Barriers: Insurance coverage for most genetic services remains inconsistent, leading to potential out-of-pocket expenses for VTS patients (Mansur et al., 2022; National Academies of Sciences, Engineering, and Medicine, 2018).
  • Disparities in Prenatal Genetic Counseling: Research indicates that women who begin prenatal care later in their pregnancies are less likely to receive genetic counseling. This trend disproportionately affects less privileged women, exacerbating existing healthcare disparities (Christopher et al., 2022).
  • Existing Guidelines and Their Limitations
Organizations such as the American College of Obstetricians and Gynecologists (ACOG), the Royal College of Obstetricians and Gynaecologists (RCOG), the International Society for Prenatal Diagnosis (ISPD), the Society for Maternal-Fetal Medicine (SMFM), and the International Society of Ultrasound in Obstetrics and Gynecology (ISUOG) have offered guidance on multiple pregnancies more broadly, but the focus on VTS is variable.
The ISUOG provides comprehensive guidance on early pregnancy ultrasound, with emphasis on the determination of chorionicity and amnionicity. In its 2025 update, ISUOG references the “vanishing twin phenomenon” during chorionicity assessment and acknowledges that earlier gestational losses may still allow for retrospective chorionicity determination (Khalil et al., 2025). However, its guidance does not extend into the clinical implications of VTS, such as placental sequelae (e.g., infarcts, hematomas, fibrosis), or psychosocial care for families affected by early loss in multiple pregnancies.
The ISPD similarly includes detailed protocols for prenatal screening and diagnosis, particularly in multifetal pregnancies, but lacks VTS-specific recommendations for interpreting cfDNA results or managing residual confounding from a demised co-twin. Although ISPD addresses limitations in cfDNA interpretation following fetal demise in general, more targeted guidance for VTS-affected pregnancies is absent.
ACOG addresses VTS primarily in the context of prenatal screening and testing. Specifically, it notes that in multifetal gestations where a fetal demise, vanishing twin, or anomaly is identified in one fetus, there is a significant risk of inaccurate test results if serum-based aneuploidy screening or prenatal cfDNA is used. In such cases, diagnostic testing should be offered (ACOG, 2020). Beyond these considerations, ACOG’s guidelines do not provide detailed recommendations for the broader clinical management of VTS, such as monitoring protocols for the surviving fetus or tailored counseling for affected parents. However, in the absence of formal guidance, expert consensus and case-based practices often include serial ultrasounds to monitor fetal growth and amniotic fluid volume, Doppler studies for assessing blood flow abnormalities (particularly in monochorionic twins), and postnatal placental evaluation (Monni et al., 2021; Weitzner et al., 2023).
SMFM does not offer a dedicated guideline for the management of VTS. However, it does reference VTS in clinical and coding guidance relevant to early pregnancy assessment and prenatal care:
  • First-Trimester Ultrasound Evaluation: SMFM emphasizes the importance of early ultrasound to establish gestational age, confirm viability, determine the number of fetuses, and identify conditions like vanishing twin or empty gestational sac. This is crucial for accurate counseling and understanding fetal risks (SMFM, 2023a).
  • Coding Guidance: SMFM provides coding recommendations for appropriately documenting cases involving a vanishing twin, which is essential for ongoing pregnancy management and insurance coverage (SMFM, 2023b).
The National Institute for Health and Care Excellence (NICE) in the United Kingdom provides comprehensive maternal health guidelines, which include antenatal management of multiple pregnancies through fetal monitoring, counseling support for parents, and screening for complications like Twin-to-Twin Transfusion Syndrome (TTTS), Twin Anemia Polycythemia Sequence (TAPS), selective fetal growth restriction (sFGR), and twin reversed arterial perfusion (TRAP) sequence (NICE 2019; Weitzner et al., 2023). NICE quality standard QS46 recommends determining chorionicity and amnionicity early in pregnancy, between 11 weeks and 2 days to 14 weeks and 1 day or as soon as possible, which has contributed to reducing twin stillbirths; however, individuals experiencing VTS were excluded from related analyses (Khalil et al., 2020; NICE, 2013). Guidelines in France, from the Collège National des Gynécologues et Obstétriciens Français (CNGOF), discuss risks associated with intrauterine fetal demise but do not specifically mention VTS (Vayssière et al., 2011).
Beyond the countries listed above, there are limited clinical guidelines specifically addressing VTS, notably across Africa, Nordic countries, Australia, China, Russia, Latin America, and the International Federation of Gynecology and Obstetrics (FIGO). Despite having the highest twinning rate of any continent and with many cultures (e.g., Yoruba) having customs surrounding the birth and death of twins in pregnancy and postpartum, a number of African nations (Rwanda, Mozambique, and Tanzania) are in need of more detailed guidelines on the management of twin pregnancies (Getchachew et al., 2024; Hanson et al., 2019; Junod, 1996; Monden et al., 2021). One exception is South Africa, which has guidelines on the management of twin pregnancies that mention potential impacts of VTS on prenatal cfDNA screening (Stewart et al., 2024). In Nordic countries (Sweden, Denmark, Norway, Finland, and Iceland), guidelines developed by the Nordic Federation of Societies of Obstetrics and Gynecology (NFOG) broadly address various obstetric scenarios, including twin deliveries, but do not specifically include VTS (NFOG, n.d.).
The Royal Australian and New Zealand College of Obstetricians (RANZCOG) also lacks formal national guidelines explicitly addressing VTS, though general obstetric guidelines address the management of multiple pregnancies (e.g., TTTS) and fetal demise in monochorionic twin pregnancies (RANZCOG, 2021). Despite the lack of guidelines in Australia, major companies like Huggies Australia, for example, provide online information on VTS, noting that while the surviving twin is usually unaffected, there is an increased risk of preterm birth and low birth weight (Huggies Australia, n.d.).
China, despite extensive research on VTS outcomes related to ART, similarly has no established national guidelines specifically for managing VTS (Li et al., 2022; Zhou et al., 2016). Studies have highlighted the association between VTS and adverse perinatal outcomes, such as preterm birth and low birth weight, but these findings have not appeared to translate into formal clinical guidelines (Li et al., 2022). In other Asian countries, such as South Korea, while there are clinical practice guidelines for prenatal aneuploidy screening and diagnostic testing, these do not specifically address VTS. The Korean Society of Maternal-Fetal Medicine (KSMFM) has developed guidelines focusing on maternal serum screening and prenatal cfDNA screening but lacks specific recommendations for managing VTS care (Choe et al., 2021).
In contrast, Canada's national guidelines, provided by the Society of Obstetricians and Gynaecologists of Canada (SOGC), acknowledge VTS explicitly, recognizing associated risks such as fetal structural anomalies, growth restrictions, and preterm birth (Public Health Agency of Canada, 2020; Weitzner et al., 2023). Given the emotional and medical complexities involved with VTS, comprehensive guidelines are needed globally to guide healthcare providers in communication, emotional and psychological care, genetic testing, and medical management following fetal loss. This may include medical management strategies such as enhanced ultrasound surveillance for the surviving fetus, placental pathology evaluation, postpartum follow-up for maternal complications, and referrals to maternal-fetal medicine specialists when warranted. The absence of formal standards can lead to significant psychological impacts such as unresolved grief, anxiety, and depression among affected families, potentially influencing parenting and intergenerational health through mechanisms such as trauma-induced epigenetic modifications (Császár & Bókkon, 2019; Song et al., 2020). Thus, establishing detailed and inclusive VTS-specific guidelines is essential to address these significant public health implications.
  • Recommendations for Future Guidelines
Future iterations of the ISUOG Practice Guidelines, along with those of other professional societies such as ISPD, ACOG, and SMFM, could be enhanced by expanding their guidance on VTS. This is particularly important following early first trimester loss, which remains the most common period for this phenomenon. Given ISUOG’s role as the leading authority on obstetric ultrasound standards and ISPD’s leadership in prenatal genetic diagnostics, both organizations are well-positioned to incorporate VTS-specific clinical implications into updated protocols. Additionally, future guidelines should integrate interdisciplinary approaches to care coordination and ensure that both patients and providers have access to standardized protocols that address bereavement support, medical procedures, and informed decision-making. In the event of a loss of multiples, the system or network of care may become even more intricate than standalone obstetric care. This is especially problematic in health systems where the burden of care is on the patient, as care can be extremely complex to navigate. Addressing these gaps through well-defined and inclusive policies will be essential in improving outcomes for individuals affected by VTS, particularly in cases occurring beyond the first trimester, where adverse outcomes in survivors and mothers have been more frequently reported.
To be effective, future guidelines should be explicit, practical, and applicable across different clinical contexts. Providers need clear protocols that address diagnostic criteria, disclosure practices, timing and interpretation of genetic testing, and bereavement support pathways. While VTS, TTTS, TAPS, sFGR, and TRAP are distinct conditions that warrant equally distinct diagnostic and care criteria, it is important for guidelines and screening protocols to account for how they can be related, as many of these conditions can lead to the loss of one or both twins (SOGC, 2023). These conditions are more likely to occur in monochorionic twins due to vascular connections in the shared placenta (i.e., placental anastomoses) (SOGC, 2023). While guidelines should emphasize the elevated risks in monochorionic twins, they must also ensure that dichorionic twins are not overlooked, as they too carry risks. Both chorionic types warrant appropriately stratified care.
Key questions remain unanswered: Should the pregnancy be managed as a twin or singleton after one fetus demises? What are the implications for maternal health, and to what degree are the surviving fetuses at neurological or hemodynamic risk due to shared placental features? Given that many of the risks associated with VTS, such as neurodevelopmental outcomes or maternal complications, are primarily documented following second- or third-trimester losses, future guidelines should clarify that current care recommendations (e.g., fetal growth monitoring, placental pathology, and mental health referrals) may be especially valuable in such cases. These practices are particularly relevant when the loss occurs later in pregnancy or when fetal remains persist throughout gestation. Evidence is still limited regarding first-trimester losses, especially in naturally conceived pregnancies, highlighting the need for tailored guidance based on timing and clinical context. It is also important to acknowledge that many of the associated risks and conditions are not specific to VTS, but reflect correlations where causality may be difficult to discern due to similarities with typical pregnancy symptoms or overlapping comorbidities.
  • Recommendations for Enhanced Care and Monitoring of Mothers and Surviving Multiples
  • For Mothers:
    • Early and Frequent Prenatal Monitoring: Initiate early prenatal visits to monitor fetal viability, assess chorionicity, and detect potential complications. When feasible, early referral to a maternal-fetal medicine (MFM) specialist is recommended.
    • Chorionicity Disclosure and Patient Education: Inform patients about chorionicity as early as possible. SNP-based cfDNA screening may aid in zygosity determination (Wojas et al., 2022), though results should be interpreted cautiously in VTS cases.
    • Genetic Counseling and Prenatal Screening Adjustments: Consider confirmatory diagnostic testing like amniocentesis or CVS. Interpret prenatal cfDNA, NT, and MSS results carefully and involve genetic counselors to assist in evaluation where necessary based on case circumstances. Alternative strategies such as nuchal translucency in combination with maternal age may be useful (ACOG, 2014). Diagnostic confirmation should be prioritized when indicated (ACOG, 2020).
    • Psychological and Bereavement Support: Offer individualized support including referrals to counseling, charities, and mental health services.
    • Resources for Handling Fetal Remains: Provide resources on funeral homes and legal definitions of remains. Consider POC testing when appropriate. Bereavement resources such as the Butterfly Project have been shown by Boutillier et al. (2023) to be particularly helpful in hospital neonatal intensive care units (NICUs).
    • Nutritional and Lifestyle Guidance: Provide tailored nutritional counseling to support maternal health and fetal development, particularly in ongoing multiple pregnancies affected by VTS. In cases where fetal resorption or placental abnormalities are suspected, nutritional support may help mitigate maternal inflammation or promote optimal growth for the surviving fetus. Emphasis should be placed on protein, folic acid, iron, and micronutrients essential for tissue repair and hematologic stability (Bibbo et al., 2022).
    • Postpartum Monitoring: Screen for delayed or secondary complications in mothers who experience VTS (e.g., hypertension and autoimmune responses). Emotional stress from unresolved grief may also contribute to somatic symptoms and should be monitored in coordination with mental health support services both during pregnancy and postpartum.
  • For Surviving Multiples:
    • NICU Readiness: Ensure access to an appropriate level NICU, especially for preterm or low birth weight infants. The NICU should ideally offer bereavement resources tailored to families experiencing the loss of a multiple (e.g., the Butterfly Project).
    • Developmental Assessments: Screen early for behavioral and cognitive issues. Monitor for congenital malformations more commonly seen after later gestational losses.
    • Routine Physical Checks: Include screening for low Apgar scores and anomalies potentially linked to vascular compromise.
    • Mental Health Monitoring: Conduct long-term psychological evaluations, particularly in monozygotic survivors.
    • Genetic Testing: Consider in rare cases of suspected chimerism.
    • Parental Education and Support: Educate parents on possible developmental or emotional impacts.
    • Multidisciplinary Care Approach: Encourage coordination among neonatologists, geneticists, psychologists, and pediatricians.
  • Rethinking the Term “Vanishing Twin Syndrome” and Exploring Additional Terminology for Survivors
The term “vanishing twin syndrome” is widely recognized, but it is medically imprecise and potentially harmful. The label suggests a process that is both final and uneventful, which may not reflect the clinical or emotional reality for patients. Instances where VTS is referred to as the “vanishing twin phenomenon” further undermines its recognition as a diagnosable obstetric event (Hayton, 2010). This vague characterization fails to convey the clinical and emotional gravity of the condition and negatively affects diagnostic accuracy, care planning, and empathetic patient communication.
Moreover, the use of the term twin (singular) or twins (plural) narrows the perceived scope of the condition, despite the fact that VTS can occur in pregnancies involving triplets or higher-order multiples. The current terminology excludes these cases by default, limiting understanding and perpetuating gaps in clinical documentation and support. In cases where fetal remains are not fully resorbed or expelled, and thus do not “vanish,” what has occurred is often a form of missed abortion (Alves et al., 2023). Future research should explore how frequently terms like “missed abortion” or “blighted ovum” are used in clinical settings to describe VTS, and how such language may influence outcomes and follow-up care.
Recognizing VTS as a miscarriage at the clinical level, whether it manifests as a blighted ovum, resorbed fetal tissue, or fetus papyraceous, aligns more accurately with existing diagnostic criteria such as “missed abortion” or “early pregnancy loss.” Framing VTS within the broader spectrum of miscarriage may improve empathy and clinical transparency, facilitate appropriate documentation, and expand access to psychosocial and bereavement support. Terminology that minimizes or oversimplifies fetal loss can shape how healthcare professionals communicate with patients, how patients interpret their experiences, and how systems prioritize care and policy development (Brann et al., 2020). Patients navigating this form of loss may be left with little clarity and even less support if the language used implies that the event was minor or self-resolving (Cubbage et al., 2025). As a result of these lingual complexities and inadequacies, existing terminology may contribute to a limited understanding of the condition’s full range and impact, affecting both patient and provider decision-making. Alternative terms such as “spontaneous co-twin demise” (in cases of twins), “intrauterine fetal demise of one twin [or triplet, etc.],” “[single/twin/triplet] fetal death in the [X] trimester,” or “intrauterine demise in a multiple gestation” offer more accurate clinical descriptions (Cleary-Goldman & D'Alton, 2004; Mackie et al., 2019; Stefanescu et al., 2021). “Vanishing” may imply an erasure or insignificance of the lost embryo, fetus, or empty gestational sac. "Vanishing twin syndrome" has been critiqued for sounding clinical, impersonal, and dismissive (Hayton, 2010). The term implies that the loss is simple or uneventful, which is often not the case emotionally or physically (Cubbage et al., 2025; Hayton, 2010).
One term proposed in the literature for the survivors of multifetal loss that has not been frequently used includes “womb twin,” which centers on the lived experience of the surviving twin, recognizing the enduring emotional and psychological impact of the prenatal loss (Hayton, 2010). “Womb twin” may also be appropriate to describe the survivors and hosts of conjoined and parasitic twins, respectively. Moreover, “womb twin” validates that a co-twin once existed and may continue to influence the survivor’s identity, health, and well-being. These alternative terms are less ambiguous and better reflect the biological, emotional, and psychological complexities most often involved with VTS, as well as other types of multifetal loss, for both pregnant individuals and survivors.
  • Conclusion
Exploring the experiences of VTS patients and improving patient care in cases of embryonic, fetal, and infant death of multiples is a multifaceted endeavor. Despite existing gaps in both academic literature and policy guidelines regarding VTS, there is a clear need for effective, evidence-based management protocols. Moving forward, addressing these gaps requires further research not only on parental VTS experiences but also on the physical and psychological trajectories of surviving VTS children. Future studies should strive to understand the informational needs, emotional and physical support requirements, and long-term outcomes of affected families. A critical component of improving care involves re-evaluating the classification of VTS within clinical and institutional frameworks. Reclassifying VTS as a form of miscarriage—particularly in cases of early embryonic or fetal loss—would align diagnostic language with patient experiences, reduce documentation inconsistencies, and enable access to bereavement resources that are otherwise unavailable. Including this reclassification in clinical guidelines could validate the grief of affected families and encourage providers to offer appropriate support. Efforts should also focus on translating research findings into comprehensive patient-centered care models. Collaboration among patient advocates, healthcare providers, researchers, and policymakers is essential for developing standards that reflect the complexity of VTS and its impact on families. Strategies for assessing intervention quality may include well-powered studies that use robust statistical analyses to evaluate outcomes, enabling evidence-based changes to care protocols.
To advance clinical practice and policy development, future research must address issues of reproducibility and generalizability. Many reported associations—such as low birth weight, placental abnormalities, and psychological sequelae—have not been consistently replicated, likely due to heterogeneity in study design, cohort selection, and confounding factors like chorionicity, amnionicity, and assisted reproductive technology (ART) use. Well-powered, prospective cohort studies are needed to disentangle outcomes specifically attributable to VTS from those associated with multifetal gestation more broadly. Incorporating stratification by gestational age at loss (e.g., first vs. later trimesters), chorionicity (e.g., monochorionic vs. dichorionic), and ART exposure into study design will enhance comparability across populations. Moreover, establishing multicenter registries to systematically document VTS diagnoses, prenatal screening results, fetal remains management, and long-term outcomes will improve data standardization and clinical benchmarking. The integration of biological samples—such as placental tissue, maternal serum, and cfDNA—into these registries can further support molecular investigations, including potential epigenetic markers or other biomarkers of VTS-related complications.

Acknowledgements

Caitlin Lee, Brigham and Women’s Hospital and Massachusetts College of Pharmacy and Health Sciences. During the preparation of this work, N.C. used ChatGPT 4.0 and 4.5 in order to reorganize and summarize sections of writing and format references. After using this tool, the author reviewed and edited the content as needed and takes full responsibility for the content of the publication.

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Table 1. Risks Linked to Vanishing Twin Syndrome: Strength of Evidence and Confounders Across Studies.
Table 1. Risks Linked to Vanishing Twin Syndrome: Strength of Evidence and Confounders Across Studies.
Risk Status in Literature Gestational Dependency Primary Citations Potential Confounders
Placental pathologies (e.g., small placentas, infarcts) Well-established across studies Across all gestational ages Batsry & Yinon, 2022; Evron et al., 2015; Khalil et al., 2025 Chorionicity, vascular events (e.g., TTTS), chromosomal aneuploidies, SARS-CoV-2 and other pathogens
Maternal psychological distress Well-established across studies Not gestation-specific; linked to diagnostic experience Cubbage et al., 2025; Highet et al., 2022; Richards et al., 2015 Healthcare interaction, cultural stigma
Intrauterine Growth Restriction (IUGR) Inconsistent results across studies More likely in second- and third-trimester losses Evron et al., 2015; Seong et al., 2020 Chorionicity, timing of demise
Vaginal bleeding Inconsistent results across studies Often in first trimester or with late loss Evron et al., 2015; Seong et al., 2020 Common in early pregnancy, nonspecific symptom
Placental abruption Inconsistent results across studies Mid-to-late gestation Seong et al., 2020 Vascular etiology, placental trauma
Cervical insufficiency Inconsistent results across studies Later gestation Seong et al., 2020 Infection, uterine anomalies
Hypertension Inconsistent results across studies Later gestation Li et al., 2023; Seong et al., 2020 ART use, pre-existing maternal conditions
Premature Rupture of Membranes (PROM) Inconsistent results across studies Typically third trimester Seong et al., 2020 Infection, chorionicity
Low birth weight Inconsistent results across studies More likely if demise occurs after 12–14 weeks Ahmed et al., 2016; Seong et al., 2020 ART, chorionicity, gestational age at loss
Low Apgar scores Inconsistent results across studies More likely with late fetal demise Roberts & Toth, 2020; Seong et al., 2020 Gestational age at loss, co-occurring pathologies
Fetal malformations (e.g., spina bifida) Inconsistent results across studies Possibly embryonic period (<8–10 weeks) Pharoah et al., 2002; Pharoah et al., 2009; Shinnick et al., 2017; Lee et al., 2023 Folate status, teratogens
Long-term stress, mood disorders in survivors Inconsistent results across studies All stages Batsry & Yinon, 2022; Song et al., 2020 Chorionicity, psychological history, zygosity
Chimerism in survivors Rare, possibly underreported More likely with early placental fusion (incl. fused DZ placentas) Fjeldstad et al., 2020; Yu et al., 2002 Testing limitations, twin DNA admixture
Epigenetic effects (e.g., methylation changes) in survivors Theoretical/emerging evidence Inter-/multi-generational relevance suggested Császár & Bókkon, 2019 Baseline variability, maternal exposures
Neurodevelopmental impairment in survivors Well-established in monochorionic twin losses; unclear in early VTS Most significant in second- to third-trimester losses in monochorionic twins Griffiths et al., 2015; Khalil et al., 2025 Chorionicity, timing of demise
Legend. Status in Literature:.
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Copyright: This open access article is published under a Creative Commons CC BY 4.0 license, which permit the free download, distribution, and reuse, provided that the author and preprint are cited in any reuse.
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