Eradication of methicillin-resistant Staphylococcus aureus with an antiseptic soap and nasal mupirocin among colonized patients – an open uncontrolled clinical trial
© Kampf and Kramer; licensee BioMed Central Ltd. 2004
Received: 11 February 2004
Accepted: 03 June 2004
Published: 03 June 2004
Aim of the study was to determine the clinical efficacy of a new antiseptic liquid soap (Stellisept® scrub), based on the combination of undecylenamidopropyltrimonium methosulphate (4%) and phenoxyethanol (2%), for eradication of MRSA among colonized patients who do not receive antibiotic therapy.
Over two years 50 MRSA patients in 6 hospitals were observed. Treatment was defined as the daily application of Stellisept scrub for the antiseptic body and hair wash (at least 60 s) in combination with nasal mupirocin. A treatment cycle was a minimum of 5 days treatment. Screening was carried out at least 48 h after the treatment cycle was finished, with 24 h between each of the requested three or more samplings, which included the nasopharynx, groin, axilla, perineum and other MRSA-positive skin areas.
Fifteen cases were retrospectively excluded (lack of outcome documentation, concomitant antibiotic therapy, open wounds). All 35 patients had colonization with MRSA before antiseptic treatment on the skin, in the groin (80%), the axilla (25.7%), the perineum (20%) or other skin areas (14.3%). Colonization at more than one skin sites was found in 34.3%. Nasal colonization was found in 21 of 28 patients (75%), 7 patients were without nasal screening prior to the antiseptic treatment. After one treatment cycle MRSA was eradicated in 25 patients (71.4%), after a second cycle the total eradication rate was 91.4%, after a third cycle the rate increased to 94.2%. No patient discontinued the antiseptic treatment due to dermal intolerance of the product.
Progressive eradication of MRSA carriage was observed with the antiseptic soap and mupirocin. The eradication rate was not biased by concomitant antibiotic treatment, screening during treatment or lack of evidence for colonization in contrast to other studies with other preparations.
Methicillin-resistant Staphylococcus aureus (MRSA) continues to be a global problem in infection control. For many years it has been a major cause for nosocomial infections in many countries [1, 2]. The proportion of methicillin resistance among clinical isolates of S. aureus is still increasing. In southern European countries, the proportion may be as high as 55% [3, 4]. MRSA now even becomes an increasing problem in the community [5, 6]. Transmission of MRSA in community has been shown to be as high as 60% . Family members who are living with MRSA carriers are in danger of MRSA transmission . Dermal colonization with MRSA may be persistent, especially in the groin . That is why attempts are often undertaken to treat colonized MRSA patients . Antibiotics were shown to be effective in uncontrolled and controlled trials with eradication rates between 53% and 85% [10–12]. But antibiotics are considered to be inappropriate for patients who are only colonized and not infected with MRSA . One reason is their potential to cause adverse effects, especially allergy, which can not be justified for patients who do not have an infection. More important is the risk of emergence of vancomycin-resistance in S. aureus . Topical antiseptic measures, however, are normally employed . The nasal cavity is usually treated with mupirocin or with tolerable antiseptics . Dermal colonization is eradicated with antiseptic liquid soaps  Only few studies have addressed the question of MRSA eradication among colonized patients with liquid soaps in combination with nasal treatment. All of them are uncontrolled trials and most of them have different types of biases.
Aim of our study was to determine the efficacy of the antiseptic soap Stellisept scrub in combination with mupirocin for eradication of MRSA among colonized patients with evidence of dermal colonization (no selection bias), without concomitant antibiotic therapy (no treatment bias) and with regular screening investigations (no outcome bias).
An open clinical trial was chosen as a study design.
Determination of MRSA carriage
The MRSA carrier status was determined before and after treatment of the patients. Swabs were taken at least from the following body sites: nasopharynx, axilla, groin and perineum. Any patient with at least one MRSA positive skin site was regarded as a patient with evidence for dermal colonization irrespective of the nasal colonization status.
All swabs were processed on the same day. Briefly, swabs were plated directly on blood agar, oxacillin resistance screening agar base (Oxoid, UK), and dextrose broth for enrichment. After incubation of plates and broth at 37°C for 18 to 24 h, colonies resembling S. aureus were identified and tested for oxacillin resistance. This was done in two steps: disk diffusion with a 5 μg oxacillin disk on Mueller-Hinton agar (incubation at 30°C for 18 – 24 h) and agar screening on Mueller-Hinton agar supplemented with 6 mg/ml oxacillin and 4% saline (Oxa Screen Test Agar, bioMérieux, France; incubation at 35°C for 24 h). Isolates growing within 14 mm around the oxacillin disk and growing on the MRSA screening plates were regarded as oxacillin resistant.
Treatment of patients
Definition of treatment and treatment cycle: Treatment was defined as the daily application of Stellisept scrub for the antiseptic body and hair wash (at least 60 s) in combination with nasal mupirocin. A treatment cycle was defined as a minimum of 5 days treatment.
Treatment of the nasal cavity
The nasal cavity was treated with mupirocin which was applied twice per day as recommended by the manufacturer (Turixin®, GlaxoSmithKline, Munich, Germany).
Treatment of the skin
The skin and hair was treated once a day with the antiseptic liquid soap (Stellisept scrub, Bode Chemie GmbH & Co., Hamburg, Germany) which is based on two active ingredients: 4% (w/w) undecylenamidopropyltrimonium methosulphate and 2% (w/w) phenoxyethanol. The minimum duration of antiseptic skin treatment was 60 s. This application time is derived from in vitro data on the activity of the product against various epidemic MRSA strains and various clinical MRSA isolates .
For body washing the skin was moistened with tap water and the liquid soap applied without dilution. Mobile patients washed themselves under supervision of a healthcare worker. Immobile patients were washed by healthcare workers. After the 60 s application residual soap had to be rinsed or washed off with tap water. Linen and clothes were changed during the antiseptic treatment and the surrounding surfaces treated with a surface disinfectant .
Patient selection and data
Six hospitals participated in the study. The local infection control nurse of a hospital was responsible for data collection. Patients were included
if there was evidence for dermal colonization with MRSA irrespective of the colonized body site (minimum screening of axilla, groin and perineum) and
if they did not receive antibiotics at the beginning of the treatment and
if they had no signs of a clinical infection and
if compliance with the treatment could be expected for the anticipated duration of hospital stay.
Patients were excluded
if antibiotics were given during the treatment or during the surveillance culture interval or
antiseptic treatment was initiated for treatment of colonized or infected wounds and
if patients were discharged before screening cultures could be obtained after treatment.
The following data were collected for each patient: gender, hospital, MRSA positive body sites before and after the antiseptic treatment (nasopharynx, axilla, groin, perineum, other body sites) and additional information if relevant for the outcome assessment. The microbiological method in each hospital for identification of MRSA from initial and follow-up swabs was not evaluated for its sensitivity and specificity since it has become routine in German laboratories.
Post treatment screening
Post treatment screening was done according to the German recommendation on MRSA patients issued by the Robert-Koch Institut . A minimum wash-out period of 48 h was required between the last treatment and the first set of screening swabs. Screening swabs had to be taken for three consecutive days and at least from the following sampling sites: nasopharynx, axilla, groin and perineum. Additional body sites were included if they were found to be MRSA positive before antiseptic treatment.
Number of patients per hospital and the type of unit of all included patients.
Intensive care unit
Frequency of MRSA detection at different body sites among 35 patients undergoing antiseptic body wash and nasal antiseptic therapy for eradication of MRSA; colonization of multiple skin sites possible.
Localisation of MRSA colonization
Before treatment (n = 35)
After treatment cycle 1 (n = 35)
After treatment cycle 2 (n = 8)
After treatment cycle 3 (n = 1)
Any skin site
▪ Upper leg
After one cycle of antiseptic body wash and concomitant nasal antisepsis with mupirocin, 25 of the 35 patients were found to be MRSA free (71.4%; Table 2). The mean duration of treatment was 6.7 ± 2.5 days. Successful eradication of MRSA was confirmed with three negative consecutive series of swabs in 16 patients (64%). Two consecutive series of swabs were negative in five patients (20%) and one series of swabs was negative in four patients (16%) which was explained by early discharge of the patient. Treatment failures after the first cycle were due to persistent colonization of the same skin area (5 of 10), colonization of another skin area (4 of 10) and persistent colonization of the nasopharynx (1 of 10). Of the remaining 10 patients, two were not treated any further due to discharge and 8 underwent a second treatment cycle with seven of them being MRSA negative afterwards (total of 91.4% being MRSA negative). The mean duration of treatment in the second cycle was 6.4 ± 2.1 days. In order to confirm successful eradication of MRSA after the second cycle, three consecutive series of swabs were negative in six patients (85.7%) and two consecutive series of swabs were negative in one patient (14.3%). The one patient remained colonized on the same skin area without nasal carriage and underwent a third treatment cycle resulting in dermal MRSA eradication (total of 94.2% being MRSA negative; Table 2). Three series of consecutive swabs were negative to confirm successful eradication of MRSA.
No patient had to discontinue the antiseptic body wash due to dermal intolerance or uncomfortable perception of the product.
Summary of clinical trials on eradication of MRSA including the colonization status before treatment, the main outcome and type of bias.
Preparation for skin antisepsis
Number of patients and colonization status (n)
Duration of treatment cycle
Overall rate of MRSA eradication
Type(s) of bias
Skin colonized: 5
Nose colonized: 5
25 days (mean)
Skin colonized: 10
Nose colonized: 18
5 days (mean)
• Early first swab (< 48 h)
• Follow-up < 7 days (n = 9)
• Selection bias (18 patients without dermal colonization)
Skin colonized: 37
Nose colonized: 57
5 days (mean)
25% (with mupirocin) 18% without mupirocin
Skin colonized: 10
Nose colonized: 8
5 – 7 days (range)
Treatment bias (all 12 patients received various antibiotics at the same time)
Triclosan soap and foam
Skin colonized: unknown
Nose colonized: unknown
4.2 days (mean)
• Selection bias (no evidence of initial dermal colonization)
• Treatment bias (concomitant antibiotic treatment to an unknown number of patients)
• Outcome bias (cultures were mainly obtained during antiseptic treatment)
Skin colonized: unknown
Nose colonized: unknown
5 days (mean)
Treatment bias (all patients received also vancomycin 250 mg every 6 h)
Trimethoprim-sulphamethoxazole (160 mg/800 mg twice daily) and rifampin (600 mg once daily) (25)
Skin colonized: unknown
Nose colonized: unknown
2 – 9 days (range)
Treatment bias: No antiseptic treatment for the skin was included
In our study, we found an eradication rate after one treatment cycle of 71.4% which is comparable to antibiotic treatment [10, 18]. After two treatment cycles, the rate was 91.4% and came up to 94.2% after a third treatment cycle. With no other antiseptic soap we were able to find comparable data which are not confounded by a lack of evidence for initial MRSA colonization, concomitant antibiotic therapy or screening cultures during antiseptic treatment.
One limitation of our study is the lack of a control. We can not exclude that washing with plain soap and water or doing nothing would not have had a similar effect regarding the eradication of MRSA, although it is very unlikely based the persistence of MRSA colonization in the groin . It would have been much more interesting to compare Stellisept scrub with either a non-medicated soap (negative control) or another antiseptic soap (e.g. based on chlorhexidine). But the use of non-medicated liquid soap would have been acting against the German recommendation for MRSA patients (antiseptic soaps or liquid preparations should be used for treatment of the skin) . The use of medicated soap, however, would have been an interesting option, ideally in a double-blind randomized design. But chlorhexidine as the most common active agent for this type of treatment has been described in recent studies with artificial contamination of fingers with MRSA to have no advantage compared with non-medicated liquid soap [19, 20]. It was therefore not considered to be suitable as a positive control . That is why an open uncontrolled design was chosen.
Another limitation is the rather short follow-up of 5 days after termination of the treatment (2 days wash-out and 3 days screening cultures). Most patients stayed as long in their hospital as it was necessary to complete the screening cultures. The main reason for even shorter follow-up is discharge of the patient from a hospital. Continuation of hospital stay with the only aim to complete screening cultures was not possible in our study. Follow-up was unknown in some studies [22, 23], shorter in others  or longer [10, 18], but in some studies not for all patients [8, 25].
Treatment failures after the first cycle were mainly observed at the same or another skin site. The surrounding may also contribute to re-colonization of a patient. It was shown in one of our cases to originate from an electric shaver which was not disinfected at all. MRSA may survive on inanimate surfaces and cotton for more than 90 days . Even making the bed leads to a large increase of MRSA in the air for 15 minutes . Careful disinfection of these possible sources and changing linen after the antiseptic treatment is therefore crucial to ensure prevention of re-colonization as recommended in the German guideline on MRSA patients .
Identification of MRSA was not carried out for all screening swabs in one laboratory but with the same test method. Differences in the sensitivity and specificity have been described [28–30] which may have an impact on the identification of a MRSA patient. But it is unlikely to have an impact on the result of the antiseptic treatment because the method would have been the same before and after treatment of the same patient. That is why it was justified not to carry out the identification of MRSA in one specific laboratory especially because recent data indicate that determination of phenotypic resistance may largely underestimate the genotypic resistance in MRSA .
Another finding is the good dermal tolerance of the antiseptic soap. All 35 patients tolerated repetitive use of the preparation very well, even more than one treatment cycle. Another preparation (Octenisept) has been described to lead to skin redness in 4 of 28 patients resulting in termination of the treatment . The excellent dermal tolerance of Stellisept scrub on intact and scarified skin has been described before .
Stellisept scrub in combination with nasal mupirocin was found to effectively and progressively eradicate MRSA from colonized patients. Antiseptic treatment may have to be repeated.
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