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. 2010 Jul 3;38(5):363–371. doi: 10.1007/s15010-010-0038-8

Table 3.

Publications describing long-term MRSA persistence

Author Study design Investigated cohort Number of investigated patients Observation period; follow-up
(months)
Principal topic Decolonisation therapy Effect of decolonisation therapy MRSA persistence dependent on anatomical site Clearance of MRSA
(days)
Significant effect of age
(years)
Comments: strengths and flaws of the publication
Scanvic et al. [15] Prospective cohort study HreAdma 78 10 (until Oct. 1998)

Colonisation and infection,

Persistence of MRSA

Not applied n.m. n.m. Percentile 50: 255 n.m.

Only re-admitted patients >3 months after previous hospital stay, were included.

No fixed timetable for control

Marschall and Muhlemann [13] Retrospective cohort study HreAdm 116 16.2 (until Dec. 2004)

Colonisation and infection,

Persistence of MRSA

Nasally applied mupirocin, washing (4%) and gargling (0.1%) with chlorhexidine MRSA loss: HR 2.22, 95% CI 1.36–3.64; p < 0.01 n.m. Percentile 60: 225 Yes

Part of patients with decolonisation 31%.

MRSA status “negative” was defined with 2 screenings with negative results

Vriens et al. [16] Retrospective cohort study HreAdm, OutPat 135

By month 24,

Median years 1.2

(Jan. 1991–Jan. 2001)

Colonisation and infection,

Persistence of MRSA

Nasally applied mupirocin, washing with chlorhexidine; for gastro-intestinal carriage systemic antibiotic therapy No data available n.m. Percentile 50: 320 n.m.

Fixed time points month 6, 12, 18, 24.

Intermittent carriers 9 (7%)

Wendt et al. [25]

Prospective randomised,

Placebo controlled double- blinded clinical trial

Study patients

56 study group,

58 placebo group

30 days (Jan. 2001–April 2004) Colonisation of skin, nares and throat Nasally applied mupirocin, washing (4%) with chlorhexidine No significant difference No n.m. n.m. Only 30 days of controlled follow-up
Harbarth et al. [23]

Prospective randomised,

Placebo controlled double- blinded clinical trial

Study patients, only non-infected

51 study group,

51 placebo group

25 (until Sept. 1997) Colonisation of skin, nares and urinary tract Nasally applied mupirocin (study group), all: 4% chlorhexidine soap for daily baths or showers No deco-lonisation-group: HR 1.55; 95% CI 0.97–2.47; p < 0.066 MRSA persistence for ≥2 bodysites: HR 1.8; 95% CI 1.1–2.9; p < 0.01 n.m. no Course of MRSA loss over a short period of 30 days after decolonisation
Buehlmann et al. [22] Prospective cohort study All MRSA-positive patients 62 36 (Jan. 2002–April 2007)

Colonisation and infection,

Persistence of MRSA

Nasally applied mupirocin, daily chlorhexidine mouth rinse and body wash for 5 days; oral vancomycin for intestinal and cotrimoxazole for urinary tract colonisation 87% of all patients after one up to 10 decolonisation cycles; 65% received peroral antibiotic treatment MRSA loss: rate after 1 decolonisation for patients with 1 body site 76.9% and 38.7% for such with multiple sites (p < 0.004) n.m. n.m.

Only repeated decolonisation courses and the use of peroral antibiotic treatment was effective for decolonisation in many cases

Ten recolonisations were typed by molecular methods, revealing eight with the same strain, one with another and one remained unknown. No time-dependent analysis and no cox-regression analysis were performed

Robicsek et al. [14] Retrospective cohort study HreAdm 648 14 (until Dec. 2007)

Colonisation or infection,

Persistence of MRSA

Nasally applied mupirocin 4% washing with chlorhexidine No significant difference in MRSA persistence found MRSA persistence for pressure ulcera: OR 2.31, 95% CI 1.28–4.19; p < 0.006 Percentile 50%: 360 No significant differences found

Course of MRSA persistence over up to 4 years; no interval data available.

Only re-admissions were considered

Present study Retrospective cohort study including all MRSA- positive patients in a university hospital HreAdm

1032

(1005)

By month 42,

Median days 44

(Jan. 2002–Nov. 2005)

Colonisation or infection,

Persistence of MRSA

Nasally applied mupirocin and daily whole body washes with octenidin for 5 days MRSA loss after decolonisation therapy during the first hospital stay for all patients: OR 2.58 95% CI 1.59- 4.21; p < 0.01 MRSA persistence for multiple bodysites: HR 2.18, 95% CI 1.52 – 3.15; p < 0.01 Percentile 50: 566a No significant differences found

Investigation of a cohort over a long time-interval.

Investigation of MRSA colonisation of different anatomical sites.

No information about the MRSA status between hospital admissions

n.m. not mentioned, HRe Adm hospital re-admission, OutPat outpatient observation of MRSA patients after discharge, OR odds ratio

aOverestimate, as no interval data have been obtained