Table 1

Characteristics of patients and of UE-DVT per group

VariableG1 (n = 23)G2 neonates (n = 25)G2 non-neonates (n = 110)P value
Age, median (25th, 75th percentile) 16 y (15, 17 y) 15 d (12, 23 d) 3.7 y (3.2 mo, 10.7 y) <.001* 
Follow-up time, median (25th, 75th percentile) 1.6 y (1.0, 2.1) 3.7 y (2.0, 6.3) 3.0 y (1.7, 4.9) <.001* 
Sex ratio (male:female) 0.8 1.5 1.2 .50 
BMI median (25th, 75th percentile) weight-for-length percentiles 64 (42, 79) −15 (<3-50) 65 (26, 86) 25 (<3-50) .99* 
Underlying conditions   <.001 
 None 23 (100%)  
 Postsurgical 20 (80%) 43 (38%)  
 CHD 15 (60%) 23 (21%)  
 Prematurity 4 (16%) 25 (23%)  
 Cancer 34 (31%)  
 IBD 10 (9%)  
Thrombophilia#    — 
 FVL homozygous 1 (4%) 1 (1%)  
 FVL heterozygous 5 (22%) 5 (6%)  
 PTG heterozygous 1 (4%) 3 (4%)  
 AT deficiency 1 (1%)  
 PS deficiency 1 (1%)  
 APS 1 (4%) 2 (2%)  
 Elevated factor VIII 1 (4%) 7 (8%)  
 Elevated Lp(a) 1 (4%)  
Causes of DVT    <.001 
 Line-related 25 (56% CVL, 44% PICC) 101 (59% PICC, 22% CVL, 15% ports, 4% other)  
 Effort/idiopathic 23 (100%)  
 Mass 6 (5%)  
 Other 3 (3%)  
Symptoms of acute DVT 23 (100%) 3 (12%) 55 (50%) <.001 
Imaging modality for DVT 5 (23%)   — 
 US  24 (96%) 95 (86%)  
 Venogram — 1 (4%) 3 (3%)  
 S+venogram 5 (23%) — 7 (6%)  
 US+MRV 2 (9%) — —  
 US+CT — — 5 (5%)  
 US+MRV+venogram 11 (45%) — —  
Therapeutic modality for DVT    <.001 
 Anticoagulant therapy 15 (65%) 25 (100%) 92 (83%)  
 Anticoagulant prophylaxis 3 (3%)  
 Thrombolysis 8 (35%)§ 2 (2%)  
 No treatment 13 (12%)  
VariableG1 (n = 23)G2 neonates (n = 25)G2 non-neonates (n = 110)P value
Age, median (25th, 75th percentile) 16 y (15, 17 y) 15 d (12, 23 d) 3.7 y (3.2 mo, 10.7 y) <.001* 
Follow-up time, median (25th, 75th percentile) 1.6 y (1.0, 2.1) 3.7 y (2.0, 6.3) 3.0 y (1.7, 4.9) <.001* 
Sex ratio (male:female) 0.8 1.5 1.2 .50 
BMI median (25th, 75th percentile) weight-for-length percentiles 64 (42, 79) −15 (<3-50) 65 (26, 86) 25 (<3-50) .99* 
Underlying conditions   <.001 
 None 23 (100%)  
 Postsurgical 20 (80%) 43 (38%)  
 CHD 15 (60%) 23 (21%)  
 Prematurity 4 (16%) 25 (23%)  
 Cancer 34 (31%)  
 IBD 10 (9%)  
Thrombophilia#    — 
 FVL homozygous 1 (4%) 1 (1%)  
 FVL heterozygous 5 (22%) 5 (6%)  
 PTG heterozygous 1 (4%) 3 (4%)  
 AT deficiency 1 (1%)  
 PS deficiency 1 (1%)  
 APS 1 (4%) 2 (2%)  
 Elevated factor VIII 1 (4%) 7 (8%)  
 Elevated Lp(a) 1 (4%)  
Causes of DVT    <.001 
 Line-related 25 (56% CVL, 44% PICC) 101 (59% PICC, 22% CVL, 15% ports, 4% other)  
 Effort/idiopathic 23 (100%)  
 Mass 6 (5%)  
 Other 3 (3%)  
Symptoms of acute DVT 23 (100%) 3 (12%) 55 (50%) <.001 
Imaging modality for DVT 5 (23%)   — 
 US  24 (96%) 95 (86%)  
 Venogram — 1 (4%) 3 (3%)  
 S+venogram 5 (23%) — 7 (6%)  
 US+MRV 2 (9%) — —  
 US+CT — — 5 (5%)  
 US+MRV+venogram 11 (45%) — —  
Therapeutic modality for DVT    <.001 
 Anticoagulant therapy 15 (65%) 25 (100%) 92 (83%)  
 Anticoagulant prophylaxis 3 (3%)  
 Thrombolysis 8 (35%)§ 2 (2%)  
 No treatment 13 (12%)  

APS, antiphospholipid syndrome; AT, antithrombin; CHD, congenital heart disease; CT, computed tomography; G1, primary UE-DVT group; G2, secondary UE-DVT group; IBD, inflammatory bowel disease; Lp(a), lipoprotein (a); MRV, magnetic resonance venogram; PICC, peripherally inserted central catheter; PS, protein S; US, Doppler ultrasound.

*

Mann-Whitney-Wilcoxon.

χ2.

Fisher exact test.

§

Local pharmaco-mechanical thrombolysis.

Systemic thrombolysis.

#

Patients tested for thrombophilia were n = 23 of 23 for G1, 16 of 25 for G2 neonates, and 84 of 110 for G2 non-neonates.

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