Page last updated: 2024-10-18

dalteparin and Systemic Inflammatory Response Syndrome

dalteparin has been researched along with Systemic Inflammatory Response Syndrome in 4 studies

Dalteparin: A low-molecular-weight fragment of heparin, prepared by nitrous acid depolymerization of porcine mucosal heparin. The mean molecular weight is 4000-6000 daltons. It is used therapeutically as an antithrombotic agent. (From Merck Index, 11th ed)

Systemic Inflammatory Response Syndrome: A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever

Research Excerpts

ExcerptRelevanceReference
"Dalteparin-treated patients received a commencement bolus of 20 units/kg and a maintenance infusion at 10 units/kg/hr."2.69A controlled trial of low-molecular-weight heparin (dalteparin) versus unfractionated heparin as anticoagulant during continuous venovenous hemodialysis with filtration. ( Cumming, AR; Gallagher, L; O'Brien, JL; Reeves, JH; Santamaria, JD, 1999)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's3 (75.00)2.80

Authors

AuthorsStudies
Keskin, H1
Keskin, F1
Yildirim, E1
Saritas, S1
Polat, G1
Colak, A1
Laloglu, F1
Guler, MA1
Ozay, M1
Alp, H1
Sochet, AA1
Morrison, JM1
Jaffray, J1
Godiwala, N1
Wilson, HP1
Thornburg, CD1
Bhat, RV1
Zia, A1
Lawrence, C1
Kudchadkar, SR1
Hamblin, F1
Russell, CJ1
Streiff, MB1
Spyropoulos, AC1
Amankwah, EK1
Goldenberg, NA1
Anastas, DC1
Farias, A1
Runyon, J1
Laufer, M1
Sendi, P1
Totapally, B1
Sachdeva, R1
Reeves, JH1
Cumming, AR1
Gallagher, L1
O'Brien, JL1
Santamaria, JD1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
COVID-19 Anticoagulation in Children - Thromboprophlaxis (COVAC-TP) Trial[NCT04354155]Phase 240 participants (Actual)Interventional2020-06-02Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Efficacy of In-hospital Thromboprophylaxis as Measured by Number of Participants With Confirmed HA-VTE

To investigate, on a preliminary basis, the efficacy of in-hospital thromboprophylaxis with twice-daily enoxaparin in children hospitalized with COVID-19, as measured by number of participants with confirmed HA-VTE. (NCT04354155)
Timeframe: Day 30

InterventionParticipants (Count of Participants)
Thromboprophylaxis2

Safety of In-hospital Thromboprophylaxis as Assessed by Number of Participants With ISTH-defined Clinically-relevant Bleeding Events During Hospitalization

"The safety of in-hospital thromboprophylaxis with twice-daily low-dose enoxaparin thromboprophylaxis will be measured by cumulative incidence (number of participants) of ISTH-defined clinically-relevant bleeding events during hospitalization. Clinically relevant bleeding episodes may include any of the following:~fatal bleeding;~clinically overt bleeding associated with a decline in hemoglobin of ≥2g/dL in a 24h period;~retroperitoneal, pulmonary, or central nervous system bleeding;~bleeding requiring surgical intervention in an operating suite;~bleeding for which a blood product is administered (blood product administration not directly attributable to the patient's underlying condition);~bleeding that requires medical or surgical intervention to restore hemostasis, other than in an operating suite." (NCT04354155)
Timeframe: Day 30

InterventionParticipants (Count of Participants)
Thromboprophylaxis0

Median Twice-daily Enoxaparin Dose Required to Achieve 4-hour Post-dose Anti-factor Xa Between 0.20-0.49 U/mL

The median twice-daily enoxaparin dose, as measured in mg/kg, required to achieve a 4-hour post-dose anti-factor Xa level of 0.20-0.49 anti-Xa U/mL in children hospitalized with COVID-19, and to compare dose-requirements by age group (<12 and those >12 years of age). (NCT04354155)
Timeframe: 4 hours post initial dose

Interventionmg/kg (Median)
Children 12 years or olderChildren less than 12 years
Thromboprophylaxis0.50.52

Trials

2 trials available for dalteparin and Systemic Inflammatory Response Syndrome

ArticleYear
Enoxaparin Thromboprophylaxis in Children Hospitalized for COVID-19: A Phase 2 Trial.
    Pediatrics, 2022, 07-01, Volume: 150, Issue:1

    Topics: Anticoagulants; Child; COVID-19; Enoxaparin; Hemorrhage; Humans; Prospective Studies; Systemic Infla

2022
A controlled trial of low-molecular-weight heparin (dalteparin) versus unfractionated heparin as anticoagulant during continuous venovenous hemodialysis with filtration.
    Critical care medicine, 1999, Volume: 27, Issue:10

    Topics: Acute Kidney Injury; Adult; Anticoagulants; Cost-Benefit Analysis; Dalteparin; Hemofiltration; Hemog

1999

Other Studies

2 other studies available for dalteparin and Systemic Inflammatory Response Syndrome

ArticleYear
Case of Venous Thromboembolia Under Enoxaparin Prophylaxis After Recovering From Acute Ischemic Stroke in Consequence of COVID-19-Related MIS-C.
    The Pediatric infectious disease journal, 2022, 05-01, Volume: 41, Issue:5

    Topics: Anticoagulants; Brain Ischemia; COVID-19; Enoxaparin; Humans; Ischemic Stroke; Systemic Inflammatory

2022
Massive Pulmonary Embolism in an Adolescent With Multisystem Inflammatory Syndrome Due to COVID-19.
    Clinical pediatrics, 2021, Volume: 60, Issue:8

    Topics: Adolescent; Computed Tomography Angiography; COVID-19; Enoxaparin; Female; Fibrinolytic Agents; Huma

2021