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Phage–Antibiotic Combination Therapy against Recurrent Pseudomonas Septicaemia in a Patient with an Arterial Stent

  • Ulla Elina Otava
  • , Laura Tervo
  • , Riikka Havela
  • , Liisa Vuotari
  • , Matti Ylänne
  • , Annette Asplund
  • , Sheetal Patpatia
  • , Saija Kiljunen*
  • *Tämän työn vastaava kirjoittaja

Tutkimustuotos: ArtikkeliTieteellinenvertaisarvioitu

11 Sitaatiot (Scopus)
28 Lataukset (Pure)

Abstrakti

Background: Intravascular stent infections are often associated with high risks of morbidity and mortality. We report here a case of a patient with an arterial stent and recurrent Pseudomonas septicaemias successfully treated with phage–meropenem combination therapy. Methods: A 75-year-old female with arteriosclerosis and comorbidities went through a femoropopliteal bypass with prosthesis in the right inguinal area. After the bypass, she developed a recurring Pseudomonas aeruginosa infection and also neutropenia during different antibiotics. A rapidly growing pseudoaneurysm in the right inguinal area led to an emergency intra-arterial stent placement during blood stream infection, later suspected to host a P. aeruginosa biofilm. Removing the stent was deemed precarious, and phage therapy was considered as a compassionate treatment option. A three-phage cocktail infecting the P. aeruginosa strain was prepared and administered intravenously together with meropenem for two weeks, after which, a ten-month follow-up was carried out. Results: No adverse reactions occurred during the phage therapy treatment, while infection markers were normalized. In addition, recovery was seen in a PET-CT scan. During the 10-month follow-up, no further P. aeruginosa septicaemias occurred. Conclusions: Phage–meropenem combination therapy was thus found safe and effective in the treatment of recurrent Pseudomonas septicaemia in a patient with an arterial stent.

AlkuperäiskieliEnglanti
Artikkeli916
JulkaisuAntibiotics
Vuosikerta13
Numero10
DOI - pysyväislinkit
TilaJulkaistu - lokak. 2024
OKM-julkaisutyyppiA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä

Rahoitus

This work was supported by the Jane & Aatos Erkko foundation (to Mikael Skurnik) and the Research Council of Finland (grant number 336519 to S.K. and PROFI7 to the University of Helsinki). Open access funding provided by University of Helsinki.

RahoittajatRahoittajan numero
Jane ja Aatos Erkon Säätiö
Helsingin yliopisto
Research Council of Finland336519
Research Council of Finland

    YK:n kestävän kehityksen tavoitteet

    Tämä tuotos edistää seuraavia kestävän kehityksen tavoitteita:

    1. SDG 3 – Hyvä terveys ja hyvinvointi
      SDG 3 – Hyvä terveys ja hyvinvointi

    Julkaisufoorumi-taso

    • Jufo-taso 1

    !!ASJC Scopus subject areas

    • Microbiology
    • Biochemistry
    • Yleinen farmakologia, toksikologia ja farmasia
    • Microbiology (medical)
    • Infectious Diseases
    • Pharmacology (medical)

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