Every year, a substantial number of children are born with congenital heart disease (CHD), a condition associated with high early mortality rates, particularly in low- and middle-income countries. Timely diagnosis and referral to centers of excellence for either surgical or percutaneous interventions can significantly improve outcomes for these children. However, in our setting, multiple systemic barriers—such as limited access to specialized pediatric cardiac surgery, a lack of awareness, poverty, illiteracy, and delayed referrals—contribute to a persistent gap between the burden of cyanotic congenital heart disease (CCHD) and the availability of adequate diagnostic and therapeutic services. In many regions, pediatric cardiac surgical facilities are entirely absent, and corrective surgeries are often delayed for years or even decades, leading to suboptimal prognoses [1-3]. The present article underscores several underrecognized, yet clinically significant, haematological abnormalities in late-presenting patients with CCHD—factors that can impact surgical outcomes but are frequently overlooked. Traditionally, the poor prognosis in these patients is primarily attributed to the severity of the underlying defect and the delayed presentation. However, this study highlights modifiable and preventable contributors, including coagulation abnormalities and hematologic imbalances, which deserve greater clinical attention [4]. Patients with CCHD are known to be at risk for both thrombotic and hemorrhagic complications. The current study reports prolonged bleeding time, prothrombin time (PT), and activated partial thromboplastin time (APTT), indicating an increased bleeding tendency, particularly during surgery. This finding is of critical importance, as bleeding risks in this population are often overshadowed by the focus on thrombosis. The correction of coagulation abnormalities in the perioperative period must be prioritized to mitigate both thrombotic and hemorrhagic complications. Moreover, platelet deficiencies and defective megakaryocyte maturation—recognized complications in these patients—can further exacerbate bleeding risks, though the study interestingly noted a low incidence of reported bleeding events despite abnormal coagulation profiles [5]. Polycythemia is a hallmark of cyanotic CHD, driven by chronic hypoxia. These patients commonly present with elevated red blood cell counts and hemoglobin levels, which can result in hyperviscosity symptoms and increased thrombotic risk. Of particular note in this study is the observation that, while most patients were polycythemic, a significant subset (12%) were found to have iron deficiency anemia. This finding is clinically relevant, as iron deficiency can exacerbate hypoxia-related symptoms and contribute to adverse perioperative outcomes, especially in surgeries involving significant blood loss. Preoperative identification and correction of iron deficiency may thus serve as an essential component of comprehensive surgical preparation. Ultimately, beyond the need for timely diagnosis and intervention, this study indirectly points toward the importance of primary prevention strategies to reduce the overall burden of CCHD. In this regard, the predictive model recently proposed by Sana Shahid et al., utilizing structural equation modeling to identify at-risk pediatric populations in Pakistan, offers a promising tool for early risk stratification and may potentially lower the incidence of CCHD in resource-limited settings [6]. This article brings to light critical, yet often neglected, aspects of preoperative assessment in children with CCHD. By identifying preventable haematological contributors to poor outcomes, it adds important evidence to the broader discussion on improving care and surgical preparedness for this vulnerable patient population. References Shahid S, Akbar A. Conventional and non-conventional risk factors of cyanotic and acyanotic congenital heart diseases in Children of Southern Punjab, Pakistan. Pakistan Heart J. 2020;53(2):132-6. DOI: 10.47144/phj.v53i2.1698 Ali F, Ladak LA, Usmani AA, Raza HA, Siddiqui MT, Hasan B. Health-related quality of life in postcardiac interventional catheterization patients with congenital heart disease: a mixed-methods study protocol from Pakistan. BMJ Open. 2021;11(12):e052989. 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