2018
DOI: 10.1016/j.anaerobe.2018.01.009
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Periprosthetic joint infection caused by anaerobes. Retrospective analysis reveals no need for prolonged cultivation time if sensitive supplemented growth media are used

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Cited by 22 publications
(16 citation statements)
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“…Waites et al demonstrated that the ingredients of commercial blood culture media are not suitable for multiplying M. hominis, confirming our negative results from incubated joint fluid (Waites and Canupp, 2001). We therefore investigated the amount of Mycoplasma hominis in LT broth, a nutritionally high-complex medium that we had evaluated for better and faster growth of anaerobes (Rieber et al, 2018). Using quantitative real-time PCR, a high bacterial concentration was detected (Table 1).…”
Section: Discussionsupporting
confidence: 71%
See 1 more Smart Citation
“…Waites et al demonstrated that the ingredients of commercial blood culture media are not suitable for multiplying M. hominis, confirming our negative results from incubated joint fluid (Waites and Canupp, 2001). We therefore investigated the amount of Mycoplasma hominis in LT broth, a nutritionally high-complex medium that we had evaluated for better and faster growth of anaerobes (Rieber et al, 2018). Using quantitative real-time PCR, a high bacterial concentration was detected (Table 1).…”
Section: Discussionsupporting
confidence: 71%
“…Aerobe and anaerobe culture on diverse agar plates remained sterile after 14 days of incubation. We have published detailed information about culture conditions for PJI elsewhere (Rieber et al, 2018). All specimens were cultured in the routinely used modified semifluid thioglycollate broth (LT) containing ox liver digest supplemented with horse serum and hemin (SIFIN, Berlin, Germany), and after seven days of incubation they all showed unevenly distributed turbidity due to agar content.…”
Section: Case Reportmentioning
confidence: 99%
“…The optimal BCB incubation time is a matter of debate [29]. Commonly, most BCBs with samples obtained from sterile sites are incubated for five days [30].…”
Section: Discussionmentioning
confidence: 99%
“…While current guidelines do not provide any advice on the duration of empirical treatment, they do recommend bacterial cultivation time up to 14 days [2,3]. Keeping the cultures two weeks is sufficient to recover almost all of the bacteria conventionally involved in PJI, including anaerobes [12,17]. The isolation of C. acnes remains a difficult topic in implant-associated infections, but it seems that in proven PJI due to this bacteria, cultures are positive in 5 to 7 days, whereas they are positive later in cases of plate contamination [18,19].…”
Section: Discussionmentioning
confidence: 99%