# Development and validation of a nomogram for predicting unplanned PICC removal in preterm infants with gestational age <32 weeks

**Authors:** Yuedi Hu, Yu Lang, Leilei Shen, Ling Yan

PMC · DOI: 10.3389/fped.2026.1725396 · Frontiers in Pediatrics · 2026-02-12

## TL;DR

This study creates a tool to predict unplanned removal of PICC lines in preterm infants, using factors like blood cell counts and insertion site to improve NICU care.

## Contribution

A novel nomogram is developed and validated for predicting unplanned PICC removal in preterm infants under 32 weeks gestational age.

## Key findings

- Five independent predictors for PICC-UR were identified: insertion site, WBC, PLT, Fib, and HCA.
- The nomogram demonstrated high accuracy with a C-index of 0.827 (95% CI: 0.740–0.915).
- Internal validation confirmed excellent calibration and clinical utility via decision curve analysis.

## Abstract

To develop and validate a risk prediction model for unplanned removal (UR) of peripherally inserted central catheters (PICC) in preterm infants with gestational age (GA) < 32 Weeks.

This retrospective study analyzed preterm infants with PICC admitted to a neonatal intensive care unit (NICU) (January 2018 to December 2024). Clinical and catheter-related variables were assessed. Multivariable logistic regression identified predictors of PICC-UR, with model performance evaluated by C-index, calibration, and decision curve analysis (internal validation via 1000 bootstraps).

We identified five independent predictors for PICC-UR: insertion site (categorical), white blood cell count (WBC), platelet count (PLT), and fibrinogen (Fib) (all modeled as continuous linear terms), along with hypercholanemia (HCA). These predictors were integrated into a nomogram designed to estimate the individual risk of PICC-UR in preterm infants. The predictive model demonstrated a high accuracy with a C-index of 0.827 [95% confidence interval (CI): 0.740–0.915]. Internal validation confirmed excellent calibration and significant clinical utility based on decision curve analysis.

This validated nomogram, incorporating insertion site, WBC, PLT, Fib and HCA, aids early identification of high-risk infants. It offers actionable insights for optimizing PICC fixation and biochemical monitoring, potentially reducing PICC-UR in NICU.

## Full-text entities

- **Genes:** FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** hepatic impairment (MESH:D008107), inflammation (MESH:D007249), vascular toxicity (MESH:D016491), pain (MESH:D010146), pneumatosis intestinalis (MESH:D011006), infants (MESH:D063766), cancer (MESH:D009369), edema (MESH:D004487), pleural effusions (MESH:D010996), GA (MESH:D016640), tachycardia (MESH:D013610), infiltrates (MESH:D017254), jaundice (MESH:D007565), Neonatal pneumonia (MESH:D011014), hypotension (MESH:D007022), HCA (MESH:C564336), vascular spasm (MESH:D020301), hypofibrinogenemia (MESH:D000347), thrombosis (MESH:D013927), death (MESH:D003643), apnea (MESH:D001049), infection (MESH:D007239), coagulopathy (MESH:D001778), cholestasis (MESH:D002779), venous thrombosis (MESH:D020246), lethargy (MESH:D053609), leukocytosis (MESH:D007964), tachypnea (MESH:D059246), thrombocytosis (MESH:D013922), necrotizing enterocolitis (MESH:D020345), abdominal distension (MESH:D000007), perforation (MESH:D057112), liver dysfunction (MESH:D017093), hyperbilirubinemia (MESH:D006932), Bloodstream Infections (MESH:D018805), PICC (MESH:D056824)
- **Chemicals:** triglycerides (MESH:D014280), D (MESH:D003903), PICC (-), bile acid (MESH:D001647), ursodeoxycholic acid (MESH:D014580), polyurethane (MESH:D011140)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12935902/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935902/full.md

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Source: https://tomesphere.com/paper/PMC12935902