- Research article
- Open Access
Successful eradication of newly acquired MRSA in six of seven patients with cystic fibrosis applying a short-term local and systemic antibiotic scheme
BMC Pulmonary Medicine volume 18, Article number: 20 (2018)
In individuals with cystic fibrosis (CF), colonization with methicillin-resistant Staphylococcus aureus (MRSA) was reported to be associated with a deterioration of pulmonary disease as reflected by an accelerated decline in lung function. Thus, an early eradication of MRSA could be beneficial in these patients. Here, we report on an intensified MRSA eradication protocol.
Since 2012 a protocol for the eradication of newly acquired MRSA has been used in our CF Clinic, combining oral rifampicin and fusidic acid, inhaled vancomycin, nasal mupirocin, local antiseptic treatment and hygienic directives all of which are applied for only 7 days during an inpatient hospital stay.
Since 2012 seven patients (3 male, 4 female; age range 4 to 30 years) newly acquired MRSA. In 6 of the 7 patients (86%) successful eradication of MRSA was achieved upon first treatment using the protocol described above. In one patient a second course of treatment was performed which, however, also failed to eliminate the colonizing MRSA.
Our protocol led to an eradication rate of 86%. The impact of each individual component of the protocol remains to be determined.
The prevalence of methicillin-resistant Staphylococcus aureus (MRSA) colonization in patients with cystic fibrosis (CF) has increased over the past years. The carrier rate significantly varies between regions, ranging from 3,4% in some CF populations in the United Kingdom  as high as 30% in the United States [2,3,4,5]. The chronic colonization with MRSA seems to be associated with a worsening of the pulmonary disease, with an accelerated decline in lung function and/or a prolonged recovery period after clinical exacerbations [1,2,3, 6, 7]. Several protocols for an early eradication of MRSA have been reported to prevent negative consequences that might result from chronic MRSA colonization [1, 2, 8]. To the best of our knowledge, studies systematically comparing these protocols are lacking in the literature, as recently also highlighted by a Cochrane review [1, 9, 10]. The aim of this retrospective study was to evaluate the efficacy of our protocol which consists of oral rifampicin and fusidic acid, inhaled vancomycin, nasal mupirocin, and hygienic directives over 7 days. This protocol has been used in our CF center since 2012.
In 2012 we established a standardized eradication protocol for newly colonized patients with CF. This protocol consists of oral rifampicin (7.5–10 mg/kg, maximum 300 mg twice daily) and oral fusidic acid (15 mg/kg maximum 500 mg three times daily). The combination of these two antibiotics seems to be effective against MRSA in CF patients [1, 8, 11]. In addition, an inhalation therapy with vancomycin (4 mg/kg, maximum 250 mg, dissolved in 4 ml sodium chloride 0,9% twice daily) is applied. None of the MRSA strains isolated from the CF patients was resistant to the above-mentioned antibiotics. Supplementary hygienic measurements including the application of mupirocin ointment and the use of disinfectants were performed as stated in Table 1. All these measures were performed under inpatient hospital conditions and contact precautions over 7 days; the inhalation therapy was supervised by a trained physiotherapist. Before starting the treatment, every family member and the pets living in the same household were also tested for MRSA. These test remained negative in each of our patients.
Since 2012 seven patients (3 male, 4 female) were newly colonized with MRSA and all were treated according to the above-mentioned protocol. The age of the patients ranged from 4 to 30 years, with a median age of 15 years. Prior to the start of the treatment each patient or its parents or legal guardian, if the patient was under 18 years old, gave oral informed consent to undergo this therapy scheme. None of the patients who were offered eradication refused to undergo the treatment, and all patients completed the treatment. New colonization with MRSA was defined by one positive culture for MRSA using either sputum analysis or an oropharyngeal swab. The cultures were performed as part of our routine monitoring, which in our CF center is carried out at least every 3 months. One patient acquired MRSA again 9 months after the first successful eradication and therefore underwent eradication for a second time. The age of the patients ranged from 4 to 30 years, with a median age of 15 years. The MRSA was either detected in sputum cultures (4 patients) or in deep oropharyngeal swabs (3 patients). Clinical data of the patients such as age, sex, and FEV1 determined at the time of MRSA detection are summarized in Table 2.
Bacterial cultures of sputum and/or of oropharyngeal swabs were obtained on day 4, 5 and 6 after the eradication attempt. If all the tests remained negative for MRSA, a successful eradication was assumed. The patients were then followed up every 3 months. In addition to the microbiological analyses a lung function test was performed if the patient was able to do it. The entire lung function tests were executed in a Master-ScreenTM Body plethysmograph (Jaeger) by a specially trained nurse.
Successful eradication was achieved in 6 of 7 patients (86%). In one patient the first eradication attempt was unsuccessful and was repeated using the same protocol, which, however, also failed. In another patient MRSA was detected again after 9 months, but was again successfully eradicated. As the MRSA isolates were not subjected to molecular typing, we cannot tell whether the patient had a recurrent colonization with the same MRSA strain or whether he acquired a new MRSA strain.
Due to the retrospective design of our study, the follow-up period of the patients varied between 7 and 38 months (median 16 months) (see Table 3 for more details).
One of the patients (number 6) that successfully underwent the MRSA eradication protocol, was too young to perform a standard lung function test. In the other patients the rate of change in FEV1% predicted varied between a decline of 8.49 per year (patient with a co-colonization with Burkholderia cepacia) and an improvement of 0.86 points. The absolute change in FEV1% predicted between the time of initial MRSA detection and the end of the follow up period is shown in Fig. 1. The details of changes in FEV1% predicted per year are shown in Table 3.
The impact of a chronic colonization with MRSA in individuals with cystic fibrosis is still a matter of debate. Some studies documented a worsening of pulmonary disease and accelerated loss of lung function in CF patients colonized with MRSA [1,2,3, 6, 7]. On the other hand, some studies suggest that acquisition of MRSA is not associated with an accelerated loss of lung function . Although a positive effect on pulmonary disease and lung function parameters is not proven yet, there are other issues that have to be considered. Because of the contact precautions, which are necessary for patients with chronic MRSA colonization, they are often unable to receive important therapeutic measures which are part of the routine treatment for CF patients in Germany: In particular the outpatient physiotherapy, which is performed once a week by a specially trained physiotherapist and the rehabilitations are frequently withheld from the patients. This might be different in other countries, but in our opinion this is an important reason to eradicate MRSA. Several CF centers therefore aim at an early eradication of MRSA immediately after its first detection. The protocols used for the eradication attempts are difficult to compare as they differ in terms of the type, administration route and duration of antibiotic therapy. The success rate of eradication observed with our protocol (86%) compares well to other published schemes, in which the success rates ranged from 55% (Solis et al.)  to 94% (Macfarlane et al.) . However, the published studies are not directly comparable, as there are many differences especially with respect to the applied antibiotics, the duration of the therapy, and the follow-up period (see Table 4 for more details). A notable advantage of our eradication protocol is its short duration of 7 days. This might not only lead to a better compliance of the patients, but should also have a positive impact with respect to side effects and the development of antibiotic resistance. The fact that the eradication scheme was performed in an inpatient hospital setting is likely to be an important factor for the high success rate, because adherence to the therapy and especially the implementation of the local measures will be higher under direct supervision than at home. In our opinion eradication according to this protocol at home would lead to a significantly lower success rate. However, as there was no control group who underwent the eradication protocol at home, this remains to be formally demonstrated. In Germany, the inpatient hospital stays are covered by the health insurances. Therefore, we have to admit that this protocol may not be feasible in other countries. Our protocol consists of three parts (local measures, oral rifampicin and fusidic acid and inhaled vancomycin). Unfortunately, we are unable to make a statement on the impact of each individual measurement on the overall success of our protocol. In particular the value of the inhaled vancomycin remains unclear. However, treatment periods longer than 7 days are probably not more successful, as we observed comparable clearance rates. In summary our protocol was well tolerated an accepted by the patients and provided an effective way to eradicate MRSA. The fact that none of the patients who have been offered the eradication procedure refused to undergo the treatment or interrupted the protocol emphasizes the compliance of the patients and the acceptance of the procedure.
Major limitations of our study are the low number of cases and the retrospective design. In addition, we used different specimens (sputum and/or deep oropharyngeal swab) to detect MRSA. This was necessary because some patients were unable to produce sputum. Previous publications suggested that cultures of oropharyngeal swabs are not reliable to predict the presence of bacterial pathogens in the lower airways of cystic fibrosis patients [14, 15]. However, given the fact that we collected three independent specimens for culture after MRSA eradication and that the patients remained negative for a median period of 16 months, we believe that the risk of a false negative result is minimal. Moreover, the heterogeneity of the patients with respect to age, sex and coinfection or co-colonization with other bacteria such as Pseudomonas aeruginosa and Burkholderia cepacia made it impossible to demonstrate a positive clinical effect of MRSA eradication in our patients. Furthermore, we were unable to compare our results to a control group of patients that were not offered eradication. A recent publication showed a spontaneous elimination of MRSA of only 26% of the affected patients . In our opinion this emphasizes the importance of MRSA eradication, which, in our opinion will be beneficial for the patients in the long run.
As mentioned above and confirmed recently by the Cochrane Collaboration [9, 10], a comparison of all published eradication schemes is not possible. Further and prospective studies comparing several eradication protocols for MRSA would be useful.
Our short term antibiotic protocol led to the eradication of newly acquired MRSA at a rate of 86%, which compares well to other published schemes. The impact of each individual component of the protocol remains to be determined.
Forced expiratory volume in one second
Methicillin-resistant Staphylococcus aureus
Methicillin-susceptible Staphylococcus aureus
Hall H, Gadhok R, Alshafi K, Bilton D, Simmonds NJ. Eradication of respiratory tract MRSA at a large adult cystic fibrosis centre. Respir Med. 2015;109(3):357–63. https://doi.org/10.1016/j.rmed.2015.01.013.
Chmiel JF, Aksamit TR, Chotirmall SH, Dasenbrook EC, Elborn JS, LiPuma JJ, et al. Antibiotic management of lung infections in cystic fibrosis. I. The microbiome, methicillin-resistant Staphylococcus Aureus, gram-negative bacteria, and multiple infections. Ann Am Thorac Soc. 2014;11(7):1120–9. https://doi.org/10.1513/AnnalsATS.201402-050AS.
Dasenbrook EC. Update on methicillin-resistant Staphylococcus Aureus in cystic fibrosis. Curr Opin Pulm Med. 2011;17(6):437–41. https://doi.org/10.1097/MCP.0b013e32834b95ed.
Harik NS, Com G, Tang X, Melguizo Castro M, Stemper ME, Carroll JL. Clinical characteristics and epidemiology of methicillin-resistant Staphylococcus Aureus (MRSA) in children with cystic fibrosis from a center with a high MRSA prevalence. Am J Infect Control. 2016;44(4):409–15. https://doi.org/10.1016/j.ajic.2015.10.015.
Salsgiver EL, Fink AK, Knapp EA, LiPuma JJ, Olivier KN, Marshall BC, et al. Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis. Chest. 2016;149(2):390–400. https://doi.org/10.1378/chest.15-0676.
Dasenbrook EC, Merlo CA, Diener-West M, Lechtzin N, Boyle MP. Persistent methicillin-resistant Staphylococcus Aureus and rate of FEV1 decline in cystic fibrosis. Am J Respir Crit Care Med. 2008;178(8):814–21. https://doi.org/10.1164/rccm.200802-327OC.
Ren CL, Morgan WJ, Konstan MW, Schechter MS, Wagener JS, Fisher KA, et al. Presence of methicillin resistant Staphylococcus Aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung function. Pediatr Pulmonol. 2007;42(6):513–8.
Macfarlane M, Leavy A, McCaughan J, Fair R, Reid AJ. Successful decolonization of methicillin-resistant Staphylococcus Aureus in paediatric patients with cystic fibrosis (CF) using a three-step protocol. J Hosp Infect. 2007;65(3):231–6.
Lo DK, Hurley MN, Muhlebach MS, Smyth AR. Interventions for the eradication of meticillin-resistant Staphylococcus Aureus (MRSA) in people with cystic fibrosis. Cochrane Database Syst Rev. 2015;2:CD009650. https://doi.org/10.1002/14651858.CD009650.pub3.
Goss CH, Muhlebach MS. Review: Staphylococcus Aureus and MRSA in cystic fibrosis. J Cyst Fibros. 2011;10(5):298–306. https://doi.org/10.1016/j.jcf.2011.06.002.
Garske LA, Kidd TJ, Gan R, Bunting JP, Franks CA, Coulter C, et al. Rifampicin and sodium fusidate reduces the frequency of methicillin-resistant Staphylococcus Aureus (MRSA) isolation in adults with cystic fibrosis and chronic MRSA infection. J Hosp Infect. 2004;56:208–14.
Sawicki GS, Rasouliyan L, Pasta DJ, Regelmann WE, Wagener JS, Waltz DA, et al. The impact of incident methicillin resistant Staphylococcus Aureus detection on pulmonary function in cystic fibrosis. Pediatr Pulmonol. 2008;43(11):1117–23. https://doi.org/10.1002/ppul.20914.
Solis A, Brown D, Hughes J, Van Saene HK, Heaf DP. Methicillin-resistant Staphylococcus Aureus in children with cystic fibrosis: an eradication protocol. Pediatr Pulmonol. 2003;36(3):189–95.
Kabra SK, Alok A, Kapil A, Aggarwal G, Kabra M, Lodha R, et al. Can throat swab after physiotherapy replace sputum for identification of microbial pathogens in children with cystic fibrosis? Indian J Pediatr. 2004;71(1):21–3.
Ramsey BW, Wentz KR, Smith AL, Richardson M, Williams-Warren J, Hedges DL, et al. Predictive value of oropharyngeal cultures for identifying lower airway bacteria in cystic fibrosis patients. Am Rev Respir Dis. 1991;144(2):331–7.
Muhlebach MS, Beckett V, Popowitch E, Miller MB, Baines A, Mayer-Hamblett M, et al. Microbiological efficacy of early MRSA treatment in cystic fibrosis in a randomised controlled trial. Thorax. 2017;72(4):318–26. https://doi.org/10.1136/thoraxjnl-2016-208949.
Kappler M, Nagel F, Feilcke M, Kroner C, Pawlita I, Naehrig S, et al. Eradication of methicillin resistant Staphylococcus Aureus detected for the first time in cystic fibrosis: a single center observational study. Pediatr Pulmonol. 2016; https://doi.org/10.1002/ppul.23519.
We would like to thank our physiotherapist team for the teaching and supervision of vancomycin inhalation and Mrs. Ines Yawa for performing the lung function test.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The ethics committee of the Friedrich Alexander Universität (FAU) Erlangen Nürnberg did not have any ethical or legal concerns about the retrospective analysis of the data reported in this manuscript.
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The authors declare that they have no competing interests.
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Kiefer, A., Bogdan, C. & Melichar, V.O. Successful eradication of newly acquired MRSA in six of seven patients with cystic fibrosis applying a short-term local and systemic antibiotic scheme. BMC Pulm Med 18, 20 (2018). https://doi.org/10.1186/s12890-018-0588-6
- Cystic fibrosis
- Methicillin- resistant Staphylococcus aureus (MRSA)