A composite splenomegaly and platelet score for thrombosis risk in myeloproliferative neoplasms in Saudi Arabia

Thrombosis is a major complication of myeloproliferative neoplasms (MPNs) and a leading contributor to morbidity and mortality, yet risk prediction data from the Middle East remain scarce, and the prevalence of silent asymptomatic thrombosis has not been well characterized. We conducted a two-center retrospective-prospective cohort study of 83 patients with Philadelphia chromosome-negative MPNs at King Faisal Specialist Hospital and Research Centre (KFSHRC), Jeddah ( n = 69) and Medina ( n = 14), Saudi Arabia (2015–2025), using 2022 WHO classification criteria. Across the full cohort, thrombosis occurred in 24 patients (28.9%), predominantly in the splanchnic/abdominal venous system (29.2%). Separately, as a prospective screening component, 45 consenting patients without previously known thrombosis underwent single-visit, comprehensive Doppler ultrasonography of the upper limbs, lower limbs, and abdominal vasculature to detect silent thrombosis. Thrombosis rates were virtually identical across both branches (Jeddah 29.0%, Medina 28.6%, p = 1.000). Splenomegaly was significantly more prevalent in thrombotic patients (70.8% [95% CI 50.8–85.1%] vs. 42.4% [95% CI 30.6–55.1%], p = 0.035). Baseline diagnostic platelet counts were paradoxically lower in the thrombosis group (median 393 vs. 682 × 10⁹/L, p = 0.020), driven by splenic sequestration - patients with splenomegaly had markedly lower baseline platelets than those without (412.5 vs. 800.0 × 10⁹/L, p = 0.005). A novel 2-variable composite score (splenomegaly + baseline PLT < 500 × 10⁹/L) produced a significant thrombosis gradient of 12.9, 33.3, and 45.5% across low, intermediate, and high-risk tiers ( p = 0.029; AUC 0.677 [95% CI 0.572–0.800]; bootstrap-corrected AUC 0.670). Established risk scores (r-IPSET-T, MIPSS-PV) demonstrated exploratory risk stratification. Systematic Prospective Doppler screening detected no new silent thrombosis (0%; 95% CI 0.0–7.9%), though larger studies are needed to definitively exclude low rates of silent thrombosis.

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Journal
Scientific Reports
Published
2026-08-03
DOI
https://doi.org/10.1038/s41598-026-64129-z
Primary Topic
Myeloproliferative Neoplasms: Diagnosis and Treatment
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article
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article

A composite splenomegaly and platelet score for thrombosis risk in myeloproliferative neoplasms in Saudi Arabia

Rania Jaha, Noha Eisa, Naif I. AlJohani, Abdulaziz Khiyami et al.
Scientific Reports
Myeloproliferative Neoplasms: Diagnosis and Treatment
article

A composite splenomegaly and platelet score for thrombosis risk in myeloproliferative neoplasms in Saudi Arabia

Rania Jaha, Noha Eisa, Naif I. AlJohani, Abdulaziz Khiyami, Dalal Aldhafeeri, Nouran Alhashimi, Mohammed Almakadi, Badr Aljoaid, Ali Alahmadi
article en

Abstract

Thrombosis is a major complication of myeloproliferative neoplasms (MPNs) and a leading contributor to morbidity and mortality, yet risk prediction data from the Middle East remain scarce, and the prevalence of silent asymptomatic thrombosis has not been well characterized. We conducted a two-center retrospective-prospective cohort study of 83 patients with Philadelphia chromosome-negative MPNs at King Faisal Specialist Hospital and Research Centre (KFSHRC), Jeddah ( n = 69) and Medina ( n = 14), Saudi Arabia (2015–2025), using 2022 WHO classification criteria. Across the full cohort, thrombosis occurred in 24 patients (28.9%), predominantly in the splanchnic/abdominal venous system (29.2%). Separately, as a prospective screening component, 45 consenting patients without previously known thrombosis underwent single-visit, comprehensive Doppler ultrasonography of the upper limbs, lower limbs, and abdominal vasculature to detect silent thrombosis. Thrombosis rates were virtually identical across both branches (Jeddah 29.0%, Medina 28.6%, p = 1.000). Splenomegaly was significantly more prevalent in thrombotic patients (70.8% [95% CI 50.8–85.1%] vs. 42.4% [95% CI 30.6–55.1%], p = 0.035). Baseline diagnostic platelet counts were paradoxically lower in the thrombosis group (median 393 vs. 682 × 10⁹/L, p = 0.020), driven by splenic sequestration - patients with splenomegaly had markedly lower baseline platelets than those without (412.5 vs. 800.0 × 10⁹/L, p = 0.005). A novel 2-variable composite score (splenomegaly + baseline PLT < 500 × 10⁹/L) produced a significant thrombosis gradient of 12.9, 33.3, and 45.5% across low, intermediate, and high-risk tiers ( p = 0.029; AUC 0.677 [95% CI 0.572–0.800]; bootstrap-corrected AUC 0.670). Established risk scores (r-IPSET-T, MIPSS-PV) demonstrated exploratory risk stratification. Systematic Prospective Doppler screening detected no new silent thrombosis (0%; 95% CI 0.0–7.9%), though larger studies are needed to definitively exclude low rates of silent thrombosis.

Scientific Reports
Mansoura University (EG), King's College London (GB), King Faisal Specialist Hospital & Research Centre (SA)
Good health and well-being
Openalex Percentile: Top 9%
Myeloproliferative Neoplasms: Diagnosis and Treatment
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