Late Vascular Occlusion of Central Lines in Pediatric Malignancies

PEDIATRICS ◽  
1998 ◽  
Vol 101 (2) ◽  
pp. e7-e7 ◽  
Author(s):  
J. A. Wilimas ◽  
M. Hudson ◽  
B. Rao ◽  
X. Luo ◽  
L. Lott ◽  
...  
Keyword(s):  
Vascular Occlusion ◽  
Central Lines ◽  
Pediatric Malignancies

scholarly journals Use of Topical Nitroglycerine in the Neonatal Population Following Peripheral Tissue Ischaemia: Case Report and Updates about Safety Concerns

2021 ◽  
pp. 1-3
Author(s):  
Lama Charafeddine ◽  
Mariam Anka ◽  
Therese Saad ◽  
Christelle Tayeh ◽  
Lama Charafeddine
Keyword(s):  
Neonatal Intensive Care ◽  
Unusual Case ◽  
Tissue Injury ◽  
Vascular Occlusion ◽  
Peripheral Tissue ◽  
Efficacy And Safety ◽  
Central Lines ◽  
Critically Ill Neonates ◽  
Local Warming ◽  
Neonatal Population

Neonatal thrombosis is a well-described morbidity occurring in the neonatal intensive care unit. Critically ill neonates are most vulnerable to developing thrombosis with serious complications. Fingers and toes ischaemia secondary to vascular occlusion following central lines insertion remains an uncommon occurrence. The therapeutic approach for peripheral tissue injury using local warming, anticoagulants, thrombolytics or topical hyaluronidase showed limited benefits and potential side effects. Here we report an unusual case of finger ischaemia treated successfully using topical nitroglycerine. This complements previous reports confirming the efficacy and safety of this drug and highlighting its potential benefit in neonates.

Effect of resistance training with vascular occlusion in the upper limbs

2020 ◽  
Vol 179 (4) ◽  
Author(s):  
João F. Barbieri ◽  
Mateus F. Camilo de Lima ◽  
Isabela Imbriani Ferreira ◽  
João P. Gomes ◽  
Shirko Ahmadi
Keyword(s):  
Resistance Training ◽  
Vascular Occlusion ◽  
Upper Limbs

TRAIL-Based Therapeutic Approaches for the Treatment of Pediatric Malignancies

2013 ◽  
Vol 20 (17) ◽  
pp. 2254-2271 ◽  
Author(s):  
C. Gasparini ◽  
L. Vecchi Brumatti ◽  
L. Monasta ◽  
G. Zauli
Keyword(s):  
Therapeutic Approaches ◽  
Pediatric Malignancies

Amniotic Fluid Embolism: Moving Diagnosis Through the Time. From the Mechanical Pulmonary Vascular Occlusion Until An Immuno - Inflammatory Pathogenesis?

2014 ◽  
Vol 14 (14) ◽  
pp. 1179-1188 ◽  
Author(s):  
Emanuela Turillazzi ◽  
Maria Neri ◽  
Stefania Bello ◽  
Irene Riezzo ◽  
Vittorio Fineschi
Keyword(s):  
Amniotic Fluid ◽  
Vascular Occlusion ◽  
Amniotic Fluid Embolism

Molecular Link between Intravascular Hemolysis and Vascular Occlusion in Sickle Cell Disease

2012 ◽  
Vol 10 (6) ◽  
pp. 756-761 ◽  
Author(s):  
Zhou Zhou ◽  
Donald L. Yee ◽  
Prasenjit Guchhait
Keyword(s):  
Sickle Cell Disease ◽  
Sickle Cell ◽  
Vascular Occlusion ◽  
Cell Disease ◽  
Intravascular Hemolysis

Methods of vascular occlusion for liver resections

2007 ◽  
Author(s):  
KS Gurusamy ◽  
Y Kumar ◽  
BR Davidson
Keyword(s):  
Vascular Occlusion ◽  
Liver Resections

scholarly journals Combination of Alcohol and EVOH as a New Embolic Agent: Midterm Tissue and Inflammatory Effects in a Swine Model

2020 ◽  
Vol 2020 ◽  
pp. 1-8
Author(s):  
Jean-François Hak ◽  
Farouk Tradi ◽  
Mickael Bobot ◽  
Pauline Brige ◽  
Paul Habert ◽  
...  
Keyword(s):  
Vascular Occlusion ◽  
Embolic Agent ◽  
Swine Model ◽  
Blood Alcohol ◽  
Alcohol Content ◽  
Ethylene Vinyl Alcohol ◽  
Blood Alcohol Content ◽  
Tubular Necrosis ◽  
Group 2 ◽  
Group 1

Objective. To evaluate the vascular occlusion and midterm tissue toxicity properties of a combination of ethylene-vinyl alcohol (EVOH) (Squid 18®) (75%) and alcohol (25%)—Alco-Squid 18—in a swine model. Materials and Methods. Alco-Squid 18 (75% Squid 18® mixed with 25% alcohol) (AS18) was compared to embolization with 96% alcohol alone and to embolization with Squid 18® (S18®) alone. An arteriovenous malformation (AVM) model was created in group 1 (n = 2). Each AVM model was then embolized with AS18 or S18® alone with evaluation of a ratio between the volume of embolic agent divided by the volume of the AVM (evaluated by CT). For group 2 (n = 5), each agent was tested on three different kidneys (upper pole kidney artery). Pre- and postinterventional CTs, angiographies, blood alcohol content dosages, and histological studies (3 months postintervention) were performed. Results. AS18 has better distal distribution than S18® alone, both in the kidneys (mean capsule-S18® distance: 3.9 mm (±0.23) and mean capsule-AS18 distance: 2.3 mm (±0.11) ( p = 0.029 ) and in the AVM model. Histological exploration found a higher rate of tubular necrosis with AS18 compared with S18® alone and alcohol alone (3.78 ± 0.44 compared to 2.33 ± 1.22 p   =  0 . 012 and 1.22 ± 0.67 p   < 0   . 0001 ). The blood alcohol content was negligible in all cases. Conclusion. AS18 can suggest a better distal sclerotic and embolic character as compared with S18® alone without systemic toxicity.

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