Multimodal Monitoring of Hemodynamics in Neonates With Extremely Low Gestational Age: A Randomized Clinical Trial
- georgschmoelzer
- Jun 8
- 3 min read
Introduction
The first 72 hours of life represent a critical window for extremely low gestational age (ELGA) neonates. During this transitional period, immature cardiac and circulatory systems adapt—sometimes precariously—to life outside the womb. Yet, how clinicians evaluate and manage transitional circulation in these high-risk infants varies widely between neonatal intensive care units (NICUs). This variation raises a pressing question: can we improve outcomes by standardizing and enhancing monitoring during this vulnerable phase?
A recent randomized clinical trial conducted in Canada sought to answer that question by investigating whether a multimodal hemodynamic monitoring approach could improve outcomes in ELGA neonates by reducing a composite marker of cardio-respiratory-renal stress known as the VVR score.
Why This Study Matters
ELGA neonates (born at 23–28 weeks’ gestation) face high risks of complications like intraventricular hemorrhage (IVH), bronchopulmonary dysplasia (BPD), and renal dysfunction. Standard clinical monitoring may not fully capture early signs of hemodynamic instability, potentially delaying interventions. This trial explored whether a targeted, multimodal approach—using early echocardiography and cerebral near-infrared spectroscopy (NIRS)—could better guide hemodynamic decisions and improve multi-organ outcomes.
Study Design and Approach
The 2-arm, unmasked randomized trial included 132 neonates born between 23.0 and 28.6 weeks’ gestation. Infants were randomized to either:
Multimodal monitoring group: Received early targeted echocardiography (TnECHO) at 18–24 and 66–72 hours and continuous cerebral NIRS for 72 hours. Clinical teams also followed a study-specific hemodynamic guideline incorporating both physiologic and biochemical data.
Standard care group: Received hemodynamic evaluation based on routine clinical-biochemical parameters without advanced monitoring tools.
The primary outcome was the VVR score at day 7—a composite index reflecting the degree of inotropic support, ventilatory burden, and renal impairment. Higher VVR scores indicate worse overall cardiorespiratory-kidney health.
Key Findings
The mean VVR score at 7 days was not significantly different between groups (16.5 in the multimodal group vs 18.9 in the standard group; P = .45).
However, peak VVR scores >53—representing extreme physiologic compromise—were only observed in the standard care group (P = .005).
Infants with these high VVR scores had dramatically higher odds of:
Death or severe IVH (OR 12.37, P = .001)
BPD (100% incidence in those with peak VVR >53)
Overall incidence of BPD was significantly lower in the multimodal group (41.3% vs 59.0%, P = .04).
Multivariate analysis identified high VVR score, late-onset sepsis, and late PDA treatment as key predictors of BPD.
Interpretation and Implications
Although the primary endpoint—mean VVR score at 7 days—was not reduced with multimodal monitoring, the approach appeared to prevent extreme deterioration and was associated with reduced BPD incidence, a critical long-term outcome.
These findings suggest that integrating tools like early echocardiography and cerebral NIRS can help clinicians detect early warning signs of hemodynamic instability and tailor interventions more effectively. The study also highlights the VVR score as a useful composite metric linking organ dysfunction to long-term morbidity.
Takeaway: More Than Just Numbers
This trial underscores a subtle but important insight: multimodal monitoring may not dramatically shift average outcomes but can reduce extreme ones—those that often result in the most devastating consequences. By avoiding severe cardio-respiratory-renal decompensation in the early days of life, we may prevent cascading complications and improve long-term health in ELGA neonates.
The next step? Larger trials and perhaps adaptive designs that integrate dynamic response to early monitoring findings. Ultimately, more personalized and physiologically-informed care could redefine what’s possible for our most fragile patients.

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