Vitamin D for prevention of sternotomy healing complications: REINFORCE-D trial
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, randomizované kontrolované studie
Grantová podpora
Ig 168602
Ministerstvo Zdravotnictví Ceské Republiky (CZ)
IG 168 601
Ministerstvo Zdravotnictví Ceské Republiky
SVV 260 263
Univerzita Karlova v Praze (CZ)
PubMed
33308291
PubMed Central
PMC7731517
DOI
10.1186/s13063-020-04920-z
PII: 10.1186/s13063-020-04920-z
Knihovny.cz E-zdroje
- Klíčová slova
- Cardiac surgery, Cholecalciferol, Healing complications, Randomized clinical trial, Sternotomy, Trial design, Vitamin D,
- MeSH
- hojení ran MeSH
- kardiochirurgické výkony * škodlivé účinky MeSH
- lidé MeSH
- pooperační komplikace etiologie prevence a kontrola MeSH
- sternotomie * škodlivé účinky MeSH
- vitamin D škodlivé účinky MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- vitamin D MeSH
BACKGROUND: Most cardiac surgery patients undergo median sternotomy during open heart surgery. Sternotomy healing is an arduous, very complex, and multifactorial process dependent on many independent factors affecting the sternum and the surrounding soft tissues. Complication rates for median sternotomy range from 0.5 to 5%; however, mortality rates from complications are very variable at 7-80%. Low calcidiol concentration below 80 nmol/L results in calcium absorptive impairment and carries a risk of bone loss, which is considered as a risk factor in the sternotomy healing process. The primary objective of this clinical trial is to compare the incidence of all postoperative sternotomy healing complications in two parallel patient groups administered cholecalciferol or placebo. The secondary objectives are focused on general patient recovery process: sternal bone healing grade at the end of the trial, length of hospitalization, number of days spent in the ICU, number of days spent on mechanical lung ventilation, and number of hospital readmissions for sternotomy complications. METHODS: This clinical trial is conducted as monocentric, randomized, double-blind, placebo-controlled, with planned enrollment of 600 patients over 4 years, approximately 300 in the placebo arm and 300 in the treatment arm. Males and females from 18 to 95 years of age who fulfill the indication criteria for undergoing cardiac surgery with median sternotomy can be included in this clinical trial, if they meet the eligibility criteria. DISCUSSION: REINFORCE-D is the first monocentric trial dividing patients into groups based on serum calcidiol levels, and with dosing based on serum calcidiol levels. This trial may help to open up a wider range of postoperative healing issues. TRIAL REGISTRATION: EU Clinical Trials Register, EUDRA CT No: 2016-002606-39 . Registered on September 8, 2016.
Department of Cardiac Surgery Na Homolce Hospital Prague Czech Republic
Department of Clinical Pharmacy Na Homolce Hospital Prague Czech Republic
Department of Medical Physics Na Homolce Hospital Prague Czech Republic
Department of Pharmacology 2nd Faculty of Medicine Charles University Prague Czech Republic
Department of Radiology Na Homolce Hospital Prague Czech Republic
Hospital Pharmacy Na Homolce Hospital Prague Czech Republic
Institute of Pharmacology 1st Faculty of Medicine Charles University Prague Czech Republic
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