Therapeutic plasma exchange in acute liver failure.
J Clin Apher
; 34(5): 589-597, 2019 Oct.
Article
em En
| MEDLINE
| ID: mdl-31348553
ABSTRACT
BACKGROUND:
Multi-organ dysfunction in acute liver failure (ALF) has been attributed to a systemic inflammatory response directly triggered by the injured liver. High-volume therapeutic plasma exchange (HV-TPE) has been demonstrated in a large randomized controlled trial to improve survival. Here, we investigated if a more cost-/ resource effective low-volume (LV) TPE strategy might have comparable beneficial effects.METHODS:
This retrospective study evaluated the effect of LV-TPE on remote organ failure, hemodynamical and biochemical parameters as well as on survival in patients with ALF. Twenty patients treated with LV-TPE in addition to standard medical therapy (SMT) were identified and 11 matched to a historical ALF cohort treated with SMT only. Clinical and biochemical parameters were recorded at admission to the intensive care unit and the following 7 days after LV-TPE.RESULTS:
Mean arterial pressure increased following first LV-TPE treatments (d0 68 [61-75] mm Hg vs d7 88 [79-98] mm Hg, P = .003) and norepinephrine dose was reduced (d0 0.264 [0.051-0.906] µg/kg/min vs d3 0 [0-0.024] µg/kg/min, P = .016). Multi-organ dysfunction was significantly diminished following LV-TPE (CLIF-SOFA d0 17 [13-20] vs d7 7 [3-11], P = .001). Thirty-day in-hospital survival was 65% in the LV-TPE cohort and 50% in the SMT cohort (Hazard-ratio for TPE 0.637; 95% CI 0.238-1.706, P = .369).CONCLUSIONS:
Patients treated with LV-TPE showed improved surrogate parameters comparable with the effects reported with HV-TPE. These data need to be interpreted with caution due to their retrospective character. Future controlled studies are highly desirable.Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Contexto em Saúde:
6_ODS3_enfermedades_notrasmisibles
Base de dados:
MEDLINE
Assunto principal:
Troca Plasmática
/
Falência Hepática Aguda
Tipo de estudo:
Etiology_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limite:
Humans
Idioma:
En
Revista:
J Clin Apher
Ano de publicação:
2019
Tipo de documento:
Article