Symptomatic Pulmonary Embolus after Catheter Removal in Children with Catheter Related Thrombosis: A Report from the CHAT Consortium

Author(s):  
Julie Jaffray ◽  
Lisa Baumann Kreuziger ◽  
Brian Branchford ◽  
Choo Phei Wee ◽  
E Vincent S Faustino ◽  
...  

Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 36-37
Author(s):  
Lisa Baumann Kreuziger ◽  
Mingen Feng ◽  
Abigail Bartosic ◽  
Pippa Simpson ◽  
Tzu-Fei Wang

Background: The duration of anticoagulation in patients with catheter-related thrombosis (CRT) has not been studied in a systematic fashion and is not standardized in clinical practice. Consensus guidelines have a weak recommendation for anticoagulation for 3 months after catheter removal in patients with upper extremity CRT, but this is mainly extrapolated from treatment of lower extremity deep vein thrombosis. Shorter durations of anticoagulation have been used in practice to balance the risk of bleeding and recurrent thrombosis; however, prospective data are lacking to evaluate the efficacy and safety of this practice. CRT is a frequent complication in the cancer population, who commonly requires central venous catheters for treatment. We proposed a prospective cohort study to determine the incidence of post-thrombotic syndrome (PTS), thrombosis recurrence, and bleeding in cancer patients with CRT treated with one month of anticoagulation after catheter removal. Methods: This is a multi-institutional prospective cohort study in patients with cancer and documented upper extremity CRT. Enrolled patients were treated with a standardized protocol with therapeutic doses of enoxaparin for one month after catheter removal. Patients with platelet count <50 x 109/L, creatinine clearance <30 ml/min, history of thrombosis, or ongoing need for catheters were excluded. Demographics, catheter data, and cancer history were collected at baseline visit when catheter was removed. Incidence of bleeding, recurrent thrombosis, PTS using the modified Villalta scale, and functional limitation using the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire were assessed at months 1, 3, and 6 after catheter removal. A modified Villalta score of 5 or higher was classified as the presence of PTS and a score of 15 or higher as severe PTS. Higher DASH scores indicated worse functional disability. Binomial tests with 95% confidence intervals (CI), Skillings-Mack and Wilcoxon signed ranks tests, and Pearson correlations on log transformed values were done. Unadjusted p-values <0.05 were considered statistically significant. Results: Twenty-seven patients from three institutions were enrolled. Seven (26%) patients discontinued study prior to month 1, with median study duration for those who continued of 176 [interquartile range (IQR): 158-186] days. The etiologies of study discontinuation were change in therapy (n=3, 11%), requiring another catheter (n=2, 7%), bleeding (n=1, 4%), and lost to follow-up (n=1, 4%). Eleven (41%) were female, and 21 (78%) were Caucasian (Table 1). Median age was 59 (IQR: 48-65) years. The most proximal location of the veins involved with the thrombus included veins proximal to subclavian (n=5, 19%), subclavian (n=6, 22%), internal jugular (n=6, 22%), and axillary (n=7, 26%). Patients with hematologic malignancies comprised 70% (n=19) of the cohort. All patients were treated with therapeutic doses of enoxaparin for a median of 32 (IQR: 30-52) days after catheter removal. During the 6-month study duration, the incidence of recurrent thrombosis was 0% (n=0/20, 95% CI: 0%-17%), and that of major hemorrhage was 5% (n=1/20, 95% CI: 0.13%-25%). Number of patients who had at least one PTS occurrence in any visit and either arm was 15% (n=3/20, 95% CI: 3.2%-38%), and no patients had severe PTS. Higher DASH scores were associated with higher PTS scores (Table 2). DASH score differed across all visits [month 1: median 6.16 (IQR: 2.08-19.97), month 3: 1.28 (0-11.67), month 6: 0 (0-10.42), p=0.040]. Pairwise comparisons revealed that no differences in DASH scores were seen between month 1 versus 6 (p=0.44) and month 3 and 6 (p=0.098). In contrast, month 6 had significantly lower and improved DASH score compared to month 1 (p=0.0066). No deaths occurred. Conclusions: Cancer patients with CRT frequently require central venous catheters. Treatment with anticoagulation for one month after catheter removal was associated with a low incidence of PTS, no recurrent thrombosis, and an improvement in functional disability over time in a cohort of 27 patients. The presence of PTS was associated with higher functional disability. Disclosures Baumann Kreuziger: Quercegen pharmaceuticals: Consultancy; CSL Behring: Consultancy.



2008 ◽  
Vol 28 (2) ◽  
pp. 130-133 ◽  
Author(s):  
Wai-Choong Lye


2017 ◽  
Author(s):  
Charles Hall ◽  
Mohamad Hamady ◽  
Taranpal Bansal ◽  
William Oldfield ◽  
Robert Thomas


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Theerawat Chalacheewa ◽  
Vanlapa Arnuntasupakul ◽  
Lisa Sangkum ◽  
Rungrawan Buachai ◽  
Jiravud Chanvitayapongs

Abstract Background Continuous peripheral nerve catheters (CPNCs) have been used for postoperative pain relief. A common problem encountered with CPNCs is pericatheter leakage, which can lead to dressing adhesive failure. Frequent dressing changes increase the risk of catheter dislodgement and infections. Adhesive glue is effective in securing the peripheral nerve catheter and decreasing leakage around the catheter insertion site. This study aimed to evaluate the incidence of pericatheter leakage with fixation using 2-octyl cyanoacrylate glue (Dermabond®) as compared to sterile strips. Methods Thirty patients undergoing unilateral total knee arthroplasty (TKA) with continuous femoral nerve catheter for postoperative analgesia were randomized into the catheter fixation with 2-octyl cyanoacrylate glue (Dermabond®) group or the sterile strip group. The primary outcome was the incidence of pericatheter leakage. Secondary outcomes included the frequent of catheter displacement, the difficulty of catheter removal, pain score and patient satisfaction. Results The incidence of pericatheter leakage at 24 and 48 h was 0% versus 93 and 0% versus 100% in the Dermabond® and sterile strip groups, respectively (P < 0.001). The incidence of displacement at 24 and 48 h was 6.7% versus 93.3 and 6.7% versus 100% in the Dermabond® and sterile strip, respectively (P < 0.001). There was no difference in numeric rating scale, difficulty of catheter removal, or satisfaction scores between groups. Conclusions Catheter fixation with 2-octyl cyanoacrylate glue (Dermabond®) decreased the incidence of pericatheter leakage, as well as catheter displacement, over 48 h as compared to sterile strip fixation. Trial registration This trial was registered on Thai clinical trial registry: TCTR20200228002, registered 24 February 2020- Retrospectively registered.



Author(s):  
Douglas Tran ◽  
Nicole Hays ◽  
Aakash Shah ◽  
Chetan Pasrija ◽  
Rafael S. Cires‐Drouet ◽  
...  


2021 ◽  
Author(s):  
Artur de Oliveira Paludo ◽  
Pedro Glusman Knijnik ◽  
Brasil Silva Neto ◽  
Milton Berger ◽  
Monish Aron ◽  
...  


2021 ◽  
pp. 112972982110087
Author(s):  
Junren Kang ◽  
Wenyan Sun ◽  
Hailong Li ◽  
En ling Ma ◽  
Wei Chen

Background: The Michigan Risk Score (MRS) was the only predicted score for peripherally inserted central venous catheters (PICC) associated upper extremity venous thrombosis (UEVT). Age-adjusted D-dimer increased the efficiency for UEVT. There were no external validations in an independent cohort. Method: A retrospective study of adult patients with PICC insertion was performed. The primary objective was to evaluate the performance of the MRS and age-adjusted D-dimer in estimating risk of PICC-related symptomatic UEVT. The sensitivity, specificity and areas under the receiver operating characteristics (ROC) of MRS and age-adjusted D-dimer were calculated. Results: Two thousand one hundred sixty-three patients were included for a total of 206,132 catheter days. Fifty-six (2.6%) developed PICC-UEVT. The incidences of PICC-UEVT were 4.9% for class I, 7.5% for class II, 2.2% for class III, 0% for class IV of MRS ( p = 0.011). The incidences of PICC-UEVT were 4.5% for D-dimer above the age-adjusted threshold and 1.5% for below the threshold ( p = 0.001). The areas under ROC of MRS and age-adjusted D-dimer were 0.405 (95% confidence interval (CI) 0.303–0.508) and 0.639 (95% CI 0.547–0.731). The sensitivity and specificity of MRS were 0.82 (95% CI, 0.69–0.91), 0.09 (95% CI, 0.08–0.11), respectively. The sensitivity and specificity of age-adjusted D-dimer were 0.64 (95% CI, 0.46–0.79) and 0.64 (95% CI, 0.61–0.66), respectively. Conclusions: MRS and age-adjusted D-dimer have low accuracy to predict PICC-UEVT. Further studies are needed.



2021 ◽  
pp. 219256822110156
Author(s):  
Ehsan Jazini ◽  
Alexandra E. Thomson ◽  
Andre D. Sabet ◽  
Leah Y. Carreon ◽  
Rita Roy ◽  
...  

Study Design: Retrospective observational cohort. Objectives: We sought to evaluate the impact of ESR on in-hospital and 90-day postoperative opioid consumption, length of stay, urinary catheter removal and postoperative ambulation after lumbar fusion for degenerative conditions. Methods: We evaluated patients undergoing lumbar fusion surgery at a single, multi-surgeon center in the transition period prior to (N = 174) and after (N = 116) adoption of ESR, comparing in-hospital and 90-day postoperative opioid consumption. Regression analysis was used to control for confounders. Secondary analysis was preformed to evaluate the association between ESR and length of stay, urinary catheter removal and ambulation after surgery. Results: Mean age study participants was 52.6 years with 62 (47%) females. Demographic characteristics were similar between the Pre-ESR and ESR groups. ESR patients had better 3-month pain scores, ambulated earlier, had urinary catheters removed earlier and decreased in-hospital opioid consumption compared to Pre-ESR patients. There was no difference in 90-day opioid consumption between the 2 groups. Regression analysis showed that ESR was strongly associated with in-hospital opioid consumption, accounting for 30% of the variability in Morphine Milligram Equivalents (MME). In-hospital opioid consumption was also associated with preoperative pain scores, number of surgical levels, and insurance type (private vs government). Pre-op pain sores were associated with 90-day opioid consumption. Secondary analysis showed that ESR was associated with a shorter length of stay and earlier ambulation. Conclusions: This study showed ESR has the potential to improve recovery after lumbar fusion for degenerative conditions with reduced in-hospital opioid consumption and improved postoperative pain scores.



CHEST Journal ◽  
2019 ◽  
Vol 156 (4) ◽  
pp. A824
Author(s):  
Junaid Habibullah ◽  
Viera Lakticova ◽  
Maksim Korotun


Sign in / Sign up

Export Citation Format

Share Document