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Inferior vena cava diameters and collapsibility index reveal early volume depletion in a blood donor model

BACKGROUND: Changes of volume status can be readily inferred from variations in diameter of the inferior vena cava (IVC) measured by ultrasound. However the effect of IVC changes following acute blood loss are not fully established. In this study, three different approaches to measuring IVC variable...

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Detalles Bibliográficos
Autores principales: Pasquero, Paolo, Albani, Stefano, Sitia, Elena, Taulaigo, Anna Viola, Borio, Lorenzo, Berchialla, Paola, Castagno, Franco, Porta, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633475/
https://www.ncbi.nlm.nih.gov/pubmed/26537114
http://dx.doi.org/10.1186/s13089-015-0034-4
Descripción
Sumario:BACKGROUND: Changes of volume status can be readily inferred from variations in diameter of the inferior vena cava (IVC) measured by ultrasound. However the effect of IVC changes following acute blood loss are not fully established. In this study, three different approaches to measuring IVC variables were compared in healthy blood donors, as a model of acute volume depletion, in order to establish their relative ability to detect acute blood loss. METHODS: Inspiratory and expiratory IVC diameters were measured before and after blood donation in hepatic long axis, hepatic short axis and renal short axis views using a 2–5 MHz curvilinear probe. All measurements were recorded and examined in real-time and post-processing sessions. RESULTS: All windows performed satisfactorily but the renal window approach was feasible in only 30 out of 47 subjects. After blood donation, IVC diameters decreased in hepatic long axis, hepatic short axis and renal short axis (expiratory: −19.9, −18.0, −26.5 %; CI 95 %: 14.5–24.1; 13.1–22.9; 16.0–35.9, respectively) (inspiratory: −31.1, −31.6, −36.5 %; CI 95 %: 21.3–40.1; 18.8–45.2; 23.4–46.0, respectively), whereas the IVC collapsibility index increased by 21.6, 22.6 and 19.3 % (CI 95 %: 11.6–42.9; 18.5–39.5; 7.7–30.0). IVC diameters appeared to return to pre-donation values within 20 min but this was only detected by the hepatic long axis view. CONCLUSIONS: IVC diameter and collapsibility index variations, as measured in M mode, consistently detect volume changes after blood donation. The longitudinal mid-hepatic approach performed better by allowing a panoramic view, avoiding anatomical aberrancies at fixed points and permitting to identify the best possible perpendicular plane to the IVC. In addition, it was able to detect time-dependent physiological volume replacement. In contrast, in our hands, the renal window could not be visualized consistently well.