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Systemic thioridazine in combination with dicloxacillin against early aortic graft infections caused by Staphylococcus aureus in a porcine model: In vivo results do not reproduce the in vitro synergistic activity.
Stenger, Michael; Behr-Rasmussen, Carsten; Klein, Kasper; Grønnemose, Rasmus B; Andersen, Thomas Emil; Klitgaard, Janne K; Kolmos, Hans Jørn; Lindholt, Jes S.
Affiliation
  • Stenger M; Research Unit of Clinical Microbiology, University of Southern Denmark, Odense, Denmark.
  • Behr-Rasmussen C; Department of Cardiothoracic and Vascular Surgery, Odense University Hospital, Odense, Denmark.
  • Klein K; Department of Vascular Surgery, Viborg Hospital, Viborg, Denmark.
  • Grønnemose RB; Research Unit of Clinical Microbiology, University of Southern Denmark, Odense, Denmark.
  • Andersen TE; Research Unit of Clinical Microbiology, University of Southern Denmark, Odense, Denmark.
  • Klitgaard JK; Research Unit of Clinical Microbiology, University of Southern Denmark, Odense, Denmark.
  • Kolmos HJ; Research Unit of Clinical Microbiology, University of Southern Denmark, Odense, Denmark.
  • Lindholt JS; Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.
PLoS One ; 12(3): e0173362, 2017.
Article in En | MEDLINE | ID: mdl-28278183
ABSTRACT

INTRODUCTION:

Conservative treatment solutions against aortic prosthetic vascular graft infection (APVGI) for inoperable patients are limited. The combination of antibiotics with antibacterial helper compounds, such as the neuroleptic drug thioridazine (TDZ), should be explored.

AIM:

To investigate the efficacy of conservative systemic treatment with dicloxacillin (DCX) in combination with TDZ (DCX+TDZ), compared to DCX alone, against early APVGI caused by methicillin-sensitive Staphylococcus aureus (MSSA) in a porcine model.

METHODS:

The synergism of DCX+TDZ against MSSA was initially assessed in vitro by viability assay. Thereafter, thirty-two pigs had polyester grafts implanted in the infrarenal aorta, followed by inoculation with 106 CFU of MSSA, and were randomly administered oral systemic treatment with either 1) DCX or 2) DCX+TDZ. Treatment was initiated one week postoperatively and continued for a further 21 days. Weight, temperature, and blood samples were collected at predefined intervals. By termination, bacterial quantities from the graft surface, graft material, and perigraft tissue were obtained.

RESULTS:

Despite in vitro synergism, the porcine experiment revealed no statistical differences for bacteriological endpoints between the two treatment groups, and none of the treatments eradicated the APVGI. Accordingly, the mixed model analyses of weight, temperature, and blood samples revealed no statistical differences.

CONCLUSION:

Conservative systemic treatment with DCX+TDZ did not reproduce in vitro results against APVGI caused by MSSA in this porcine model. However, unexpected severe adverse effects related to the planned dose of TDZ required a considerable reduction to the administered dose of TDZ, which may have compromised the results.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Staphylococcal Infections / Staphylococcus aureus / Thioridazine / Dicloxacillin / Vascular Grafting Type of study: Prognostic_studies Limits: Animals Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Document type: Article Affiliation country: Dinamarca

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Staphylococcal Infections / Staphylococcus aureus / Thioridazine / Dicloxacillin / Vascular Grafting Type of study: Prognostic_studies Limits: Animals Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Document type: Article Affiliation country: Dinamarca