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https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4507
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DC Field | Value | Language |
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dc.contributor.author | Ullman, Amanda | en |
dc.contributor.author | Byrnes, J. | en |
dc.contributor.author | Keogh, S. | en |
dc.contributor.author | Kleidon, T | en |
dc.contributor.author | Paterson, R. S. | en |
dc.contributor.author | Cattanach, P. | en |
dc.contributor.author | Gibson, V. | en |
dc.contributor.author | Takashima, M. | en |
dc.contributor.author | Bradford, N. | en |
dc.contributor.author | Cooke, M. | en |
dc.contributor.author | Rickard, C. M. | en |
dc.contributor.author | Paton, A. | en |
dc.contributor.author | Roy, J. | en |
dc.contributor.author | Walker, R. | en |
dc.contributor.author | Edwards, R. | en |
dc.date.accessioned | 2022-11-07T23:53:29Z | - |
dc.date.available | 2022-11-07T23:53:29Z | - |
dc.date.issued | 2022 | en |
dc.identifier.citation | , 2022 | en |
dc.identifier.other | RIS | en |
dc.identifier.uri | http://dora.health.qld.gov.au/qldresearchjspui/handle/1/4507 | - |
dc.description.abstract | BACKGROUND: Central venous access devices (CVADs) are integral to cancer care provision. Despite the high prevalence of CVAD complications in children with cancer, preventative strategies are understudied. OBJECTIVE: The aim of this study was to assess study feasibility, occlusive events, thrombolytic use, adverse events, and direct costs of catheter lock solutions. METHODS: A single-center, parallel-group, pilot randomized controlled trial was undertaken at a tertiary-referral pediatric hospital in Australia. Children 18 years or younger with an oncological or malignant hematological condition and a CVAD were eligible. Participants were 1:1 randomized to (1) normal or (2) heparinized (10-100 U/mL; CVAD-type dependent) saline lock solutions. RESULTS: Of 217 children assessed for eligibility, 61 were recruited and randomized to normal (n = 30; 3850 CVAD days) or heparinized (n = 31; 4036 CVAD days) saline. Eligibility (52%) and recruitment (54%) feasibility targets were not met. Protocol adherence was high (95% assessments), with no attrition. Parent/clinician satisfaction of interventions was high (median, 10/10 clinicians/parents). Complete CVAD occlusion occurred in heparin only (n = 2, 6.7% CVADs; incidence rate [IR], 0.49/1000 CVAD days [0.06-1.78]). Central venous access device partial occlusion was detected in 23.3% of CVADs in heparin (n = 7; IR, 2.73/1000 CVAD days [1.36-4.87]) and 13.8% of CVADs in normal saline (n = 4; IR, 2.59/1000 CVAD days [1.24-4.77]). Thrombolytic agents were used in 16.7% heparin (5 CVADs) and 3.5% normal saline (1 CVAD). Adverse events did not differ between groups. CONCLUSION: Multisite randomized controlled trials examining CVAD locks are safe, but strategies and resources to increase recruitment and eligibility are required. IMPLICATIONS FOR PRACTICE: Both routine CVAD lock solutions seem safe but may not prevent all forms of CVAD-associated harm.L6372028832022-02-15 <br /> | en |
dc.language.iso | en | en |
dc.relation.ispartof | Cancer nursing | en |
dc.title | Routine Catheter Lock Solutions in Pediatric Cancer Care: A Pilot Randomized Controlled Trial of Heparin vs Saline | en |
dc.type | Article | en |
dc.identifier.doi | 10.1097/NCC.0000000000001053 | en |
dc.subject.keywords | catheter | en |
dc.subject.keywords | articleAustralia | en |
dc.subject.keywords | feasibility study | en |
dc.subject.keywords | female | en |
dc.subject.keywords | human | en |
dc.subject.keywords | human experiment | en |
dc.subject.keywords | incidence | en |
dc.subject.keywords | major clinical study | en |
dc.subject.keywords | male | en |
dc.subject.keywords | malignant neoplasm | en |
dc.subject.keywords | multicenter study | en |
dc.subject.keywords | occlusion | en |
dc.subject.keywords | child | en |
dc.subject.keywords | patient referral | en |
dc.subject.keywords | pediatric hospital | en |
dc.subject.keywords | protocol compliance | en |
dc.subject.keywords | randomized controlled trial | en |
dc.subject.keywords | satisfaction | en |
dc.subject.keywords | fibrinolytic agent | en |
dc.subject.keywords | heparin | en |
dc.subject.keywords | sodium chloride | en |
dc.subject.keywords | eligibility | en |
dc.subject.keywords | parallel design | en |
dc.subject.keywords | clinical assessment | en |
dc.subject.keywords | clinical trial | en |
dc.subject.keywords | controlled study | en |
dc.relation.url | https://www.embase.com/search/results?subaction=viewrecord&id=L637202883&from=exporthttp://dx.doi.org/10.1097/NCC.0000000000001053 | | en |
dc.identifier.risid | 2212 | en |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairetype | Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
Appears in Sites: | Children's Health Queensland Publications Queensland Health Publications |
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