What available evidence is there for the usage of MRSA nasal PCR for infections outside of the respiratory tract?

Comment by InpharmD Researcher

The evidence behind the usage of MRSA nasal PCR for infections outside of the respiratory tract is primarily retrospective and varies by infection type. In skin and soft tissue infections, particularly in high-prevalence areas, a negative swab does not reliably exclude MRSA; however, it may support de-escalation in cases of nonpurulent cellulitis or diabetic foot infections. For intra-abdominal and urinary tract infections, where MRSA is rarely a causative pathogen, screening generally offers limited utility, though in healthcare-associated cases, its high negative predictive value (NPV) may help guide therapy. Among immunocompromised patients, such as those post-transplant or with leukemia, limited data suggest MRSA screening may aid decision-making in select situations. In critically ill patients or those with suspected bloodstream infections, MRSA nasal PCR should not be used alone to guide therapy. Please refer to Tables 1-11 for studies evaluating the use of MRSA nasal PCR across various non-respiratory tract infections.

Background

Methicillin-resistant Staphylococcus aureus (MRSA) nasal screening has demonstrated effectiveness in reducing the duration of vancomycin therapy for lower respiratory tract infections; however, its applicability to other types of infections remains unclear. Due to this uncertainty, a 2018 literature review aimed to evaluate the utility of MRSA nasal screening beyond lower respiratory tract infections. Regarding nonspecific (any source) infections, a retrospective review of 273 patients assessed MRSA nasal screening alongside blood, wound, or respiratory cultures within 48 hours of hospital admission, showing sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of 58.3%, 93.9%, 30.4%, and 98.0%, respectively. In another retrospective study of 11,882 intensive care unit patients, only 0.22% of those with negative MRSA nasal swab results developed clinically significant MRSA infections, resulting in a high NPV of 99.4%. Notably, it was estimated that 7,364 days of vancomycin therapy could have been avoided if vancomycin had been discontinued in patients with negative swab results. [1]

For bloodstream infections, a retrospective review of patients with S. aureus bacteremia (N= 409) found that MRSA swab results obtained within the previous 30 days had NPV greater than 95% and 90% if the proportion of MRSA bloodstream isolates was less than 19.3% and 33.5%, respectively. Another retrospective cohort study of MRSA screening in patients with S. aureus bacteremia (N= 799) showed a sensitivity of 56%, specificity of 98%, PPV of 88%, and NPV of 91%. Although it was concluded that a negative MRSA nasal screening was not accurate enough to rule out MRSA bacteremia, it was suggested that a positive MRSA nasal swab should prompt consideration for initiation of anti-MRSA therapy. Subgroup analyses of larger studies also showed varying performance of MRSA nasal screening in predicting MRSA bloodstream infections, indicating inconsistencies in effectiveness. The authors suggest that empiric vancomycin may be necessary regardless of nasal screening, especially if there's a risk of bloodstream infection from other methicillin-resistant gram-positive bacteria. A positive MRSA nasal screen might prompt consideration for anti-MRSA therapy in high-risk patients, despite typically low PPVs. While routine incorporation of MRSA nasal screening in managing S. aureus bacteremia seems unlikely, it could be useful in stable patients without risk factors for methicillin-resistant pathogens. [1]

Notably, guidelines recommend empiric vancomycin for patients with healthcare-associated intra-abdominal infections known to be colonized with MRSA or at risk due to prior treatment failure and significant antibiotic exposure, while advising against empiric anti-MRSA therapy for patients with community-acquired intra-abdominal infections. Limited evidence exists on the performance of MRSA nasal screening in predicting intra-abdominal infections, with studies reporting varying sensitivities and specificities. Despite this, MRSA nasal screening results provide additional data to consider when deciding to initiate or de-escalate anti-MRSA therapy, potentially leading to improved patient outcomes and cost savings. The implementation of universal MRSA nasal screening prior to major gastrointestinal surgery could potentially prevent surgical site infections and yield significant cost savings. [1]

Regarding skin and soft tissue infections (SSTI) and bone and joint infections, retrospective studies have shown varying performances of MRSA nasal screening. For SSTI, one study reported a sensitivity of 60.0%, a specificity of 71.8%, a PPV of 6.6%, and an NPV of 98.1%. Conversely, in diabetic foot infections, MRSA nasal screening demonstrated a sensitivity of 41%, specificity of 90%, PPV of 67%, and NPV of 80%. Additionally, a retrospective evaluation of MRSA screening in 102 patients with prosthetic joint infections secondary to Staphylococcus spp. reported overall poor performance, with neither sensitivity nor NPV exceeding 80%. However, the prevalence of MRSA infection in this study was high (37%) compared to other evaluated studies. These findings suggest challenges in predicting MRSA infection, particularly in contexts with high MRSA prevalence. Importantly, the authors emphasize that prospective data on using MRSA nasal screening for de-escalation of empiric therapy in SSTI are currently lacking. [1]

At the time of this review's publication, no independent studies assessed the efficacy of MRSA nasal screening for predicting MRSA urinary tract infections (UTI). However, two large retrospective reviews conducted subgroup analyses for UTI patients, reporting sensitivities ranging from 71.0% to 77%, specificities from 79.3% to 87%, PPV from 11% to 13.3%, and NPV exceeding 98%. Although MRSA nasal screening shows promise as a tool for guiding empiric antibiotic selection and de-escalation in UTIs, MRSA is uncommon in urinary pathogens, with a prevalence of less than 5%, and empiric anti-MRSA therapy is rarely warranted in this context. As for central nervous system infections, the performance of MRSA nasal screening remains unexplored, raising concerns about its safety in guiding antibiotic selection for high-risk meningitis patients. Overall, the authors suggest that MRSA nasal screening serves as a valuable antimicrobial stewardship tool, extending its potential applications beyond lower respiratory tract infections. Negative MRSA nasal screening in appropriately selected patients can prevent unnecessary initiation or guide discontinuation of anti-MRSA therapy. However, further investigation of MRSA nasal screening's clinical utility for non-respiratory tract infections is warranted as its usage becomes more widespread. [1]

Similarly, another review article published in 2022 discusses the role of MRSA nasal swabs in guiding empiric antibiotic therapy for various infections. The predictive value of MRSA nasal screening varies by clinical syndrome and patient population. For skin and soft tissue infections, especially purulent infections in areas with high MRSA prevalence, a negative nasal swab does not reliably rule out MRSA, and empiric anti-MRSA therapy remains appropriate. However, in hospitalized patients with diabetic foot infections or nonpurulent cellulitis, a negative swab may support de-escalation of MRSA-targeted therapy. For intra-abdominal infections, MRSA is an uncommon pathogen in community-acquired cases, and screening is generally not indicated. In health care–associated cases, the high NPV of a nasal swab may help avoid or de-escalate anti-MRSA therapy. Similarly, for urinary tract infections, where MRSA is rarely implicated, MRSA screening offers limited benefit. Among immunocompromised patients, such as those with leukemia or post-transplant, data are limited, but high NPVs suggest a possible role for MRSA screening in de-escalating therapy in selected situations. Importantly, in critically ill patients with septic shock or suspected bloodstream infections, empiric antibiotic decisions should not rely on MRSA nasal screening results alone. Overall, MRSA nasal screening is best used to rule out MRSA infection due to its high NPV across various clinical scenarios, while a positive swab should not be used alone to justify anti-MRSA therapy. [2]

A 2018 systematic review and meta-analysis further investigated the potential role of MRSA colonization in determining the need for empiric coverage. A total of 29 studies were included, with 24,225 patients. Results revealed that in infectious cases where the pathogen was either not known or included organisms other than Staphylococcus aureus, pooled specificities for bacteremia, lower respiratory tract infections, and skin and soft tissue infections (SSTI) were greater than 85%. For SSTIs specifically, sensitivity was 54.0% (95% confidence interval [CI] 37.7 to 69.4) and specificity was 92.9% (95% CI 90.7 to 94.5). In most instances where the prevalence of MRSA as a causative organism is <15%, the negative NPV of a negative MRSA colonization swab was found to be > 90%. [3]

Lastly, a 2023 single-center, before-and-after study examined vancomycin overuse between May 2020 and June 2021, aiming to investigate the effectiveness of MRSA nasal screenings for de-escalating vancomycin therapy in patients suspected of MRSA infections. The study included adult patients with suspected MRSA infections such as pneumonia, intra-abdominal infections, bacteremia, and skin infections, while excluding urinary tract infections. Each patient undergoing the intervention was swabbed in the nares prior to vancomycin administration. Vancomycin therapy days were measured before and after the intervention including the number of swabs collected after the implementation of the intervention. The intervention led to a significant increase in the use of vancomycin nares swabs (28/150 vs. 48/100, p= 0.040) immediately pre/post-intervention, and a notable decrease in vancomycin usage days per 1,000 patient days by 2.34% per month (p= 0.0039) over a two-year period post-intervention, demonstrating the efficacy of MRSA nasal screenings in reducing unnecessary vancomycin therapy in various types of infections outside the respiratory tract. [4]

References:

[1] Carr AL, Daley MJ, Givens Merkel K, Rose DT. Clinical Utility of Methicillin-Resistant Staphylococcus aureus Nasal Screening for Antimicrobial Stewardship: A Review of Current Literature. Pharmacotherapy. 2018;38(12):1216-1228. doi:10.1002/phar.2188
[2] Liu C, Holubar M. Should a MRSA Nasal Swab Guide Empiric Antibiotic Treatment?. NEJM Evid. 2022;1(12):EVIDccon2200124. doi:10.1056/EVIDccon2200124
[3] Butler-Laporte G, De L'Étoile-Morel S, Cheng MP, McDonald EG, Lee TC. MRSA colonization status as a predictor of clinical infection: A systematic review and meta-analysis. J Infect. 2018;77(6):489-495. doi:10.1016/j.jinf.2018.08.004
[4] Gentges J, El-Kouri N, Rahman T, Mushtaq N, Hudson E, Scheck D. Use of nares swab to de-escalate vancomycin for patients with suspected methicillin-resistant Staphylococcus aureus. Antimicrob Steward Healthc Epidemiol. 2023;3(1):e167. Published 2023 Oct 9. doi:10.1017/ash.2023.444

Literature Review

A search of the published medical literature revealed 11 studies investigating the researchable question:

What available evidence is there for the usage of MRSA nasal PCR for infections outside of the respiratory tract?

Level of evidence

C - Multiple studies with limitations or conflicting results  Read more→



Please see Tables 1-11 for your response.


Clinical utility of methicillin-resistant Staphylococcus aureus nasal polymerase chain reaction (PCR) assays beyond respiratory infections
Design

Retrospective cohort study

N= 1,989

Objective To determine the clinical utility of MRSA nasal PCR assays beyond respiratory indications by estimating its predictive value for clinical cultures from blood, bone, and soft-tissue infections
Study Groups All patients (N= 1,989)
Inclusion Criteria Patients aged ≥18 years who had a MRSA nasal PCR during a hospital admission and had a clinical culture obtained within 3 days of the MRSA PCR order date
Exclusion Criteria Patients with multiple hospital encounters within the study period were only evaluated for the first encounter, with both MRSA nasal PCR and clinical culture data available
Methods MRSA nasal PCR was performed using GeneXpert GX-XVI and DX System version 4.8 software. Clinical cultures included blood, soft-tissue, deep podiatric wound, bone, joint aspirate, or synovial fluid cultures. Data were collected via manual review of electronic medical records.
Duration March 1, 2019, to February 29, 2020
Outcome Measures Specificity and negative predictive value of MRSA nasal PCR for blood, bone, and soft-tissue cultures
Baseline Characteristics Characteristic All patients (N= 1,989)
Male 54.6%
Median age, years (IQR) 66 (54-77)
Diabetes mellitus 659 (33.1%)
Renal replacement therapy 75 (3.8%)
Results Endpoint Any Clinical Culture, % (95% CI) Blood Cultures, % (95% CI) Bone and Soft-Tissue Cultures, % (95% CI)
Prevalence 12.3% (10.9–13.8) 12.3% (10.9–13.8) 12.9% (8.2–18.8)
Sensitivity 67.5% (50.9–81.4) 81.8% (59.7–94.8) 55.0% (31.5–76.9)
Specificity 88.8% (87.3–90.2) 88.5% (86.9–89.8) 92.7% (87.3–96.3)
Positive Predictive Value (PPV) 11.0% (7.4–15.6) 7.5% (4.5–11.6) 50.0% (28.2–71.8)
Negative Predictive Value (NPV) 99.3% (98.7–99.6) 99.8% (99.4–99.9) 92.7% (87.3–96.3)
Adverse Events Not applicable
Study Author Conclusions A negative MRSA nasal swab obtained within 3 days of a culture has a high negative predictive value for MRSA infections in blood, bone, and soft tissues, supporting the use of MRSA nasal PCR assays to guide antibiotic de-escalation beyond pneumonia. 
InpharmD Researcher Critique The study's retrospective design and smaller sample size for bone and soft-tissue cultures may limit the generalizability of the findings. The study did not account for the time discrepancies between MRSA nasal PCR order and collection, which could affect the results. Additionally, the study focused on microbiological findings without clinical outcome data. 
References:

Noeldner HM, Bliek ZJ, Jones NE, et al. Clinical utility of methicillin-resistant Staphylococcus aureus nasal polymerase chain reaction (PCR) assays beyond respiratory infections. Antimicrob Steward Healthc Epidemiol. 2022;2(1):e108. Published 2022 Jun 30. doi:10.1017/ash.2022.256

 

Utility of MRSA nares PCR for non-respiratory cultures in critically ill patients: an observational evaluation
Design

Single-center, retrospective, cohort evaluation

N= 200

Objective

To evaluate the clinical utility of MRSA nares PCR in non-respiratory cultures in critically ill patients

Study Groups

All patients (n= 200)

Inclusion Criteria

Admitted to Critical Care Medicine with a positive culture collected/obtained 48h prior to, or within seven days after, a MRSA nares PCR

Exclusion Criteria

Indeterminate MRSA PCR result, receipt of nasal decolonisation within two weeks prior to PCR, treatment with anti-MRSA antibiotic(s) for at least 48h or anytime within seven days prior to culture collection, or a history of empyema, necrotising lung infection, or cystic fibrosis

Methods

Retrospective cohort evaluation of critically ill patients admitted and discharged between 1/1/2019 and 8/31/2022. MRSA nares PCR results were used in combination with microbiology reports of ICU patients with positive blood, urine, and/or wound cultures. Cultures were documented as deep, superficial, or tissue. Outcomes evaluated were NPV, PPV, sensitivity, and specificity of MRSA nares PCR.

Duration

January 2019 to August 2022

Outcome Measures

NPV, PPV, sensitivity, and specificity of MRSA nares PCR

Baseline Characteristics   All patients (n= 200)

Age, years 

61 ± 16

Diabetes

88 (44%)

Receiving COVID-19 treatment

71 (36%)

Chronic obstructive pulmonary disease

29 (15%)

Immunocompromised

9 (5%)

Patients with >1 culture

53 (27%)

Reason for admission

Respiratory

Infectious diseases

Other

Cardiovascular

Neurological

Gastrointestinal/genitourinary

 

103 (52%)

36 (18%)

22 (11%)

16 (8%)

16 (8%)

7 (4%)

Source*

Blood

Urine

Wound

Deep 

Tissue 

Superficial

 

124 (48%)

87 (34%)

48 (18%)

41 (86%)

4 (8%)

3 (6%)

*Patients may have more than one culture

Results

Culture Type

NPV (95% CI) PPV (95% CI) Sensitivity (95% CI) Specificity (95% CI)

All cultures (n= 259)

98.6 (96.3 to 99.5)  22.2 (15.7 to 30.5)  76.9 (46.2-95)  85.8 (80.8 to 89.9)

Blood (n= 124)

97.1 (92.7 to 98.8) 31.8 (20 to 46.5) 70 (34.8 to 93.3) 86.8 (79.2 to 92.4)

Urine (n= 87)

100 (94.9 to 100) - - 80.5 (70.6 to 88.2)

Wound (n= 48)

100 (91.6 to 100) 50 (25.1 to 74.9) 100 (29.2 to 100) 93.3 (81.7 to 98.6)
Adverse Events

Not applicable

Study Author Conclusions

A negative MRSA nares PCR may be used to withhold initiation or allow for timely de-escalation of anti-MRSA antibiotics in critically ill patients if clinically applicable

Critique

The study provides valuable insights into the utility of MRSA nares PCR in critically ill patients, demonstrating high NPV for non-respiratory cultures. However, the study is limited by its retrospective design, small sample size for wound cultures, and the low prevalence of MRSA, which may affect the generalizability of the findings. Additionally, the study did not include culture-negative patients, which could have influenced the NPV and PPV results. Further prospective studies are needed to confirm these findings and determine the optimal timing for MRSA nares PCR in relation to culture obtainment.

References:

Rodriguez A, Rich RL, Semanco M. Utility of MRSA nares PCR for non-respiratory cultures in critically ill patients: an observational evaluation. Infect Dis (Lond). 2025;57(4):361-365. doi:10.1080/23744235.2024.2438822

 

Evaluation of the Negative Predictive Value (NPV) of Methicillin-Resistant Staphylococcus aureus (MRSA) Nasal Swab Screening in the Medical Intensive Care Units (MICU) and Its Effect on Antibiotic Duration

Design

Retrospective, single-center study

N= 338 patients

Objective

To investigate the negative predictive values (NPVs) of methicillin-resistant Staphylococcus aureus (MRSA) nasal swabs in the medical intensive care units (MICU) and evaluate the impact of MRSA nasal swab screening on the treatment duration of empirical glycopeptide therapy (teicoplanin or vancomycin)

Study Groups

With MRSA nasal screening (n= 277)

Without MRSA nasal screening (n= 61)

Inclusion Criteria

Age ≥ 20 years-old; receiving glycopeptide therapy in the ICU (only those who had MRSA nasal screening within 7 days before or 2 days after they started receiving glycopeptide therapy were included)

Exclusion Criteria

Treated with glycopeptide therapy for over 2 days before MICU admission; died during glycopeptide therapy; had other indications for glycopeptide therapy

Methods

The NPV of MRSA nasal swabs for MRSA infection was calculated, and their influence on empirical glycopeptide treatment duration was analyzed. Positive MRSA culture result was defined as the specimen from blood, urine, sputum and catheter of a patient revealed MRSA within 7 days after nasal screening. 

Duration

January 1, 2019, to December 31, 2019

Outcome Measures

Sensitivity, specificity, positive predictive value (PPV), and NPV of the MRSA nasal swabs; treatment duration of empirical glycopeptide therapy

Baseline Characteristics

 

Without Screening

(n=32)

With Screening

(n=122)

All Patients

(n=154)

Age, year

65.3±13.1

64.6±14.9

64.7±14.5

Male

20 (62.5%) 86 (70.5%) 106 (68.8%)

APACHE II score

23.5±9.7 24.6±7.7 24.4±8.2

MRSA carrier

N/A 2 (1.6%) --

Prior culture isolation of MRSA in the last 90 days

1 (3.1%) 4 (3.3%) 5 (3.2%)

Receipt of parenteral antibiotics in the last 90 days

31 (96.9) 107 (87.7%) 138 (89.6%)

Recent hospitalization > 2 days in the last 90 days

31 (96.9%) 103 (84.4%) 134 (87.0%)

APACHE II= Acute Physiology and Chronic Health Evaluation II score

Results

NPV, PPV, Sensitivity and Specificity of MRSA Nasal Screening by Types of Infections

 

Pt, n PPV, % NPV, % Sensitivity % Specificity %

Whole screening cohort

277 71.4 98.4 78.9 97.7

Types of infections

Pneumonia

170 80.0 98.1 80.0 98.1

Bloodstream infection

18 75.0 100.0 100.0 93.3

Sepsis

50 33.3 97.9 50.0 95.8

Intra-abdominal infection

28 100.0 100.0

Skin and soft tissue infection

18 50.0 93.8 50.0 93.8

Urinary tract infection

5 0.0 100.0 80.0

Head and neck infection

10 100.0 100.0 100.0 100.0

Patients with or without MRSA Nasal Screening in Medical Intensive Care Units

 

Without Screening

(n=32) 

With Screening

(n=122) 

All Patients

(n=154)

 

p-value

Treatment days

4.4±3.0

4.2±2.8

4.3±2.8

0.577

Adverse Events

Adverse Events: N/A

Study Author Conclusions

The MRSA nasal swabs have high NPV for MRSA infection in critically ill patients. However, it has no impact on the empirical glycopeptide treatment duration. The value of MRSA nasal swabs should be advocated to optimize antibiotic therapy.

InpharmD Researcher Critique

This study shows that nasal swabs were not only applicable to respiratory tract specimens but also had extremely high NPVs in the bacterial culture results of specimens in other sites (eg, blood, catheters, and urinary catheters). However, this study has inherent limitations, including its retrospective single-center design. Additionally, the NPV of the study may not be generalizable to other ICUs with different MRSA prevalence rates. Moreover, the judgment of MRSA infection in this study was based on the diagnosis of clinicians and the culture results. Since the MRSA colonization and infection were not truly distinguished, the true subsequent MRSA infection rate may be even lower.



References:

Tai CH, Liu WL, Pan SC, Ku SC, Lin FJ, Wu CC. Evaluation of the Negative Predictive Value of Methicillin-Resistant Staphylococcus aureus Nasal Swab Screening in the Medical Intensive Care Units and Its Effect on Antibiotic Duration. Infect Drug Resist. 2022;15:1259-1266. Published 2022 Mar 24. doi:10.2147/IDR.S351832

 

Nasal-Swab Results for Methicillin-Resistant Staphylococcus aureus and Associated Infections

Design

Retrospective chart review

N= 273

Objective

To describe the diagnostic characteristics of nasal-swab screening in predicting methicillin-resistant staphylococcus aureus (MRSA) infections in hospitalized patients receiving empiric treatment with intravenous (IV) vancomycin

Study Groups

Study cohort (n= 273)

Inclusion criteria

Age ≥ 18 years, initiated on empiric IV vancomycin within 48 hours of admission, documented MRSA nasal swab, culture of samples from at least one of the following sites, drawn within 48 hours of admission: blood, sputum, wound, bronchoalveolar lavage (BAL), and/or endotracheal tube

Exclusion criteria

Bacterial culture collected after first vancomycin dose, long-term dialysis therapy

Methods

Data was compiled via a retrospective chart review at a tertiary care center in Canada.

Outcome Measures

Culture results, swab sensitivity and specificity

Baseline Characteristics

 

Study cohort (n=273)

Age, years

55.8 ± 17.7

Male

176 (64.5%)

History of recent admission within three months

73 (26.7%)

Culture

Blood

Wound

Sputum

BAL

 

266 (79.6%)

36 (10.8%)

9 (2.7%)

1 (0.3%)

Results

 

MRSA culture result   
Nasal swab result

Positive

Negative Total
Positive

7

16 23
Negative

5

245 250
Total

12

261 273
 

% Sensitivity (95% CI)

% Specificity (95% CI) Positive predictive value (95% CI) Negative predictive value (95% CI)
All cultures

58.3 (28.6-83.5)

93.9 (90.0–96.3) 30.4 (14.1-53.0) 98 (95.1-99.3)

CI, confidence interval

Study Author Conclusions

Given the high specificity of this rapid method, clinicians should ensure that patients who are receiving empiric treatment for MRSA infection and who have a positive result on nasal-swab screening continue to receive MRSA coverage until culture results are available. The high negative predictive value and positive likelihood ratio for nasal-swab screening in a low-prevalence setting suggest that a negative result significantly reduces the probability of MRSA infection.

InPharmD Researcher Critique

Being a retrospective chart review, some confounding factors would not have been accounted for in this study, such as quality and consistency of nasal swabs and patients who may have received MRSA treatment outside of the study site. 

References:

Rioux J, Edwards J, Bresee L, et al. Nasal-Swab Results for Methicillin-Resistant Staphylococcus aureus and Associated Infections. Can J Hosp Pharm. 2017;70(2):107-112. doi:10.4212/cjhp.v70i2.1642

Clinical Utility of Negative Methicillin-Resistant Staphylococcus Aureus (MRSA) Nasal Surveillance Swabs in Skin and Skin Structure Infections

Design

Retrospective, cohort analysis

N= 473

Objective

To determine the clinical utility of MRSA swabs for identifying MRSA-associated skin and skin structure infections (SSSIs) and the potential effects on antimicrobial stewardship efforts

Study Groups

MRSA-positive nasal swab (n= 156)

MRSA-negative nasal swab (n= 317)

Inclusion Criteria

MRSA nasal swab test performed during the visit and had a primary diagnosis of a SSSI

Exclusion Criteria

Readmission during the time period evaluated, duplicate encounters, <18 years of age at the time of admission, both a positive and a negative MRSA nasal swab result during the same admission

Methods

Data on baseline characteristics, culture data, and antibiotic data were retrospectively collected via electronic medical records.

Duration

Between July 1, 2014, and June 30, 2020

Outcome Measures

Primary: duration of vancomycin therapy

Secondary: positive predictive value, negative predictive value, sensitivity, specificity

Baseline Characteristics

 

MRSA-positive nasal swab (n= 156)

MRSA-negative nasal swab (n= 317)

 

Age, years (range)

59 (45 to 71)

58 (47 to 69)

 

Male

88 (56.4)

180 (56.8)

 

Weight, kg (range)

78 (68 to 100)

86 (68 to 105)

 

Height, cm (range)

173 (163 to 180)

170 (163 to 180)

 

Race

White

Black

Other

 

112 (71.8%)

43 (27.6%)

1 (0.6%)

 

200 (63.1%)

103 (32.5%)

14 (4.4%)

 

SSSI location

Face

Head

Trunk

Upper extremities

Lower extremities

Multiple sites

Unspecified

 

12 (7.7%)

2 (1.3%)

36 (23.1%)

25 (16.0%)

44 (28.2%)

2 (1.3%)

35 (22.4%)

 

11 (3.5%)

1 (0.3%)

66 (20.8%)

53 (16.7%)

103 (32.5%)

6 (1.9%)

77 (24.3%)

 

Cultures collected

65 (41.7%)

158 (49.8%)

 

MRSA organism Isolated

35 (22.4%)

8 (2.5%)

 

Prior anti-MRSA therapy in 3 mo

24 (15.4%)

72 (22.7%)

 

Total duration of all antibiotic therapy, days

6 (4 to 12)

7 (4 to 12)

 

Length of stay, days

10 (4 to 19)

8 (4 to 17)

 

Results

Endpoint

MRSA-positive nasal swab (n= 156)

MRSA-negative nasal swab (n= 317)

p-value

Vancomycin utilization outcomes (IQR)

Duration of vancomycin therapy, days

Doses of vancomycin administered

Number of vancomycin levels collected

 

4 (3 to 6)

6 (3 to 10)

2 (1 to 4)

 

3 (2 to 5)

5 (3 to 8)

2 (1 to 3)

 

0.01

0.03

0.43

Prognostic test statistics, % (95% CI)

Sensitivity

Specificity

Negative predictive value

Positive predictive value

 

81.4 (66.1 to 91.1)

71.9 (67.3 to 76.0)

97.5 (94.9 to 98.8)

22.4 (16.3 to 29.9)

Interquartile range, IQR; confidence interval, CI

Adverse Events

N/A

Study Author Conclusions

Patients with a negative MRSA nasal swab received approximately one day less of vancomycin, which represented a decrease in drug administered. The negative predictive value for SSSIs is promising, showing potential for the role of MRSA nasal swabs in de-escalating therapy.

InpharmD Researcher Critique

Limitations include the retrospective nature, small sample size, lack of culture data, and inability to account for any anti-MRSA therapies given completely outpatient or solely in the emergency department. Despite a statistically significant difference in the primary outcome, its clinical implications are uncertain. Furthermore, the primary outcome of duration was solely based on vancomycin and did not account for other anti-MRSA therapies that patients may have been switched to (e.g., linezolid, doxycycline, or sulfamethoxazole/trimethoprim).

References:

Burgoon R, Weeda E, Mediwala KN, et al. Clinical utility of negative methicillin-resistant Staphylococcus aureus (MRSA) nasal surveillance swabs in skin and skin structure infections [published online ahead of print, 2021 Dec 25]. Am J Infect Control. 2021;S0196-6553(21)00846-4. doi:10.1016/j.ajic.2021.12.005

 

Determining the Utility of Methicillin-Resistant Staphylococcus Aureus Nares Screening in Antimicrobial Stewardship

Design

Retrospective cohort study

N= 561,325 clinical cultures (245,833 unique patients)

Objective

To determine the negative predictive value (NPV) of Methicillin-Resistant Staphylococcus Aureus (MRSA) screening in the determinization of subsequent positive clinical culture for MRSA

Study Groups

Whole cohort (N= 561,325)

Inclusion Criteria

All VA patients; aged ≥18 years; were tested for MRSA colonization via the nares upon admission or transfer to a VA inpatient facility

Exclusion Criteria

Discharge nares results; rectal swabs for vancomycin-resistant Enterococci; autopsy results; cultures with disparate results (e.g., a blood culture with a comment labeled as an abscess); cases where the collection sample type was missing

Methods

Data from patients with MRSA nares screening upon admission or transfer were retrospectively collected from the VA Corporate Data Warehouse (based on VA medical centers nationwide). Subsequent clinical cultures within 7 days of the nares swab were evaluated for presence of MRSA. 

Duration

From January 1, 2007 to January 1, 2018

Outcome Measures

Sensitivity, specificity, positive predictive values (PPVs), NPVs

Baseline Characteristics

 

Whole cohort (N= 561,325)

 

     

Age, years

68.2 ± 12.3        

Male

540,583 (96.3%)        

Results

Endpoint

Sensitivity (95% confidence interval [CI])

Specificity

PPV

NPV

p-value

Whole cohort (N= 561,325)

67.4%; (67.0%-67.9%) 81.2%; (81.1%-81.3%) 24.6%; (24.4%- 24.8%) 96.5%; (96.4%- 96.52%) < 0.0001

Blood culture (n= 70,185)

69.8%; (68.7%-71.0%) 81.9%; (81.6%-82.2%) 27.8%; (27.4%- 28.3%) 96.5%; (96.3%- 96.6%) < 0.0001

Intra-abdominal culture (n= 

11,906)

66.1%; (61.4% -70.6%) 89.3%; (88.7% -89.8%) 18.8%; (17.5% - 20.1%) 98.6%; (98.4% - 98.8%) < 0.0001

Respiratory culture (n= 

90,912)

76.2%; (75.4% -77.0%) 80.3%; (80.0% -80.6% 35.0%; (34.6% - 35.3%) 96.1%; (95.9% - 96.2%) < 0.0001

Wound culture (n= 

136,078)

59.8%; (59.1% -60.5% 82.5%; (82.3% -82.7%) 34.2%; (33.8% - 34.6%) 93.1%; (93.0% - 93.3%) < 0.0001

Urinary system culture (n= 

201,443)

72.5%; (71.1% -73.8%) 80.2%; (80.0% -80.4%) 7.6%; (7.4% - 7.7%) 99.2%; (99.2% - 99.3%) < 0.0001

Adverse Events

N/A

Study Author Conclusions

Given the high NPVs, MRSA nares screening may be a powerful stewardship tool for de-escalation and avoidance of empirical anti-MRSA therapy.

InpharmD Researcher Critique

The study suggests that a negative MRSA nares swab, when taken within 7 days of culture, appears to be useful to predict the absence of MRSA in subsequent clinical culture. However, the retrospective nature of this study allowed for inconsistencies with available data for collection. Furthermore, some of the positive cultures may have not been true infections, and patients could have been colonized with MRSA in other body sites other than the nares such as the rectum and axilla, which would not have been captured in this study. 

References:

Mergenhagen KA, Starr KE, Wattengel BA, Lesse AJ, Sumon Z, Sellick JA. Determining the utility of methicillin-resistant staphylococcus aureus nares screening in antimicrobial stewardship. Clin Infect Dis. 2020;71(5):1142-1148. doi:10.1093/cid/ciz974

Does a Positive Methicillin-Resistant Staphylococcus aureus (MRSA) Nasal Screen Predict the Risk for MRSA Skin and Soft Tissue Infection?

Design

Single-center, retrospective cohort study

N= 300

Objective

To determine whether MRSA nasal screening predicts the risk of MRSA skin and soft tissue infections (SSTIs)

Study Groups

Total cohort (N= 300)

MRSA-positive nasal swab (n= 50)

MRSA-negative nasal swab (n= 250)

Inclusion Criteria

Patients ≥18 years of age, had an MRSA nasal screen and wound culture obtained within 48 hours of starting antibiotics 

Exclusion Criteria

MRSA nasal screen and wound culture not obtained during the same encounter, wound culture not obtained within 48 hours of antibiotic initiation, diagnosis of SSTI not confirmed during admission, susceptibilities for wound cultures growing MRSA were not available

Methods

Patients with wound culture results and MRSA nasal screen results were obtained from the microbiology department and performed at a tertiary care, academic medical center.

Duration

December 1, 2018 to October 31, 2021

Outcome Measures

Primary: MRSA nasal screening results predict the likelihood of MRSA SSTIs (assessed by utilizing sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), positive likelihood ratio (PLR), and pretest and posttest probabilities)

Baseline Characteristics

 

Full cohort (N= 300)

Male gender, n (%)

181 (60.3)

Age (years), mean (±SD)

56 (15.3)

Weight (kg), mean (±SD)

91.8 (31.1)

Diabetes, n (%)

138 (46.0)

Chronic renal replacement therapy

Hemodialysis, n (%)

Peritoneal dialysis, n (%)

 

6 (2.0)

4 (1.3)

Purulence, n (%) 157 (52.3)
Empiric MRSA coverage, n (%) 273 (91.0)

Culture type

Swab, n (%)

Incision and drainage, n (%)

OR culture, n (%)

IR-guided aspiration, n (%)

 

139 (46.3)

103 (34.3)

47 (15.7)

11 (3.7) 

Infection diagnosis

Abscess, n (%)

Cellulitis, n (%)

Ulcer, n (%)

Wound with osteomyelitis, n (%)

Surgical site infection, n (%)

Burn, n (%)

Multiple diagnoses, n (%)

 

108 (36.0)

50 (16.7)

41 (13.7)

37 (12.3)

18 (6.0)

10 (3.3)

10 (3.3)

Results

 

Total cohort (n= 300)

MRSA prevalence (95% CI)

18.3% (14.2% to 23.3%)

Sensitivity, (95% CI)

63.6% (49.5% to 75.9%)
Specificity, (95% CI) 93.9% (89.9% to 96.4%)
PPV, (95% CI) 70.0% (55.2% to 81.7%)
NPV, (95% CI) 92.0% (87.7% to 94.9%)
PLR, (95% CI) 10.39 (6.12 to 17.65)

Pretest

Probability (%)

Odds

 

18.3

0.2245

Posttest odds

Positive

Negative

 

2.3333

0.0870

Posttest probability (%)

Positive

Negative

 

70.0

8.0

Confidence Interval, CI

Adverse Events

Common Adverse Events: N/A 

Study Author Conclusions

In a cohort of patients at our institution, a positive MRSA nasal screen was associated with a large increase in the probability of MRSA SSTI, and a negative MRSA nasal screen was associated with a small but potentially significant decrease in the probability of MRSA SSTI. These results augment existing literature in this area and may further improve empiric antibiotic therapy guidance for patients with SSTIs. Additional data are needed to determine the clinical role of MRSA nasal screening in guiding SSTI antibiotic therapy.

InpharmD Researcher Critique

This study focused on patients with culturable wounds, so its findings may not be applicable to SSTIs that are nonculturable, such as nonpurulent cellulitis. 

 
References:

Hitchcock AM, Seabury RW, Kufel WD, et al. Does a Positive Methicillin-Resistant Staphylococcus aureus (MRSA) Nasal Screen Predict the Risk for MRSA Skin and Soft Tissue Infection?. Ann Pharmacother. 2023;57(6):669-676. doi:10.1177/10600280221127389

 

MRSA nares swab is a more accurate predictor of MRSA wound infection compared with clinical risk factors in emergency department patients with skin and soft tissue infections

Design

Prospective, observational study

N= 116

Objective

To determine the predictive value of methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage for skin and soft tissue infections (SSTI) caused by MRSA and whether MRSA nasal carriage better identifies patients with MRSA infection compared with other risk factors

Study Groups

Study cohort (N= 116)

Inclusion Criteria

SSTI clinical diagnosis by EM provider

Exclusion Criteria

Wound culture was not obtained; hospital admission was required; odontogenic infection; Bartholin gland abscess; surgical site infection or animal/human bite

Methods

Patients were screened using the ED research associate (EDRA) program, then provided swabs of anterior nares. EM clinical pharmacists evaluated positive infection site cultures for appropriate treatment per existing practice.

Duration

Between May 2010 and November 2011

Outcome Measures

MRSA prediction of wound culture for nares swab and risk factors

Baseline Characteristics

 

Study cohort (N= 116)

 

   

Age, years

32.8 ± 11.4      

Male

69 (59.5%)      

White

57 (49.1%)      

Medical history

Previous SSTI

Previous SSTI (last 12months)

Diabetes mellitus

Injection drug use

Immunosuppressed

Hemodialysis

 

73 (62.9%)

53 (45.7%)

17 (14.7%)

13 (11.2%)

2 (1.7%)

2 (1.7%)

     

Type of infection at ED presentation

Abscess

Cellulitis

Abscess/cellulitis

Ulcer

Ulcer/abscess

Paronychia

Pilonidal cyst

Erysipelas

 

72 (62.1%)

24 (20.7%)

19 (16.4%)

2 (1.7%)

0

1 (0.9%)

0

0

     

Results

Endpoint

Sensitivity (95% CI)

Specificity (95% CI)

PPV (95% CI)

NPV (95% CI)

Risk factors

Nares swab

MRSA prescription coverage

 

57.7 (44.3 to 71.1)

59.6 (46.3 to 73.0)

 

92.2 (85.6 to 98.8)

34.4 (22.7 to 46.0)

 

85.7 (74.1 to 97.3)

50.6 (46.9 to 54.4)

 

72.8 (63.2 to 82.5)

68.6 (63.3 to 73.9

Abbreviations: CI= confidence interval; NPV= negative predictive value; PPV= positive predictive value

The most common organism isolated from wound culture was S. aureus (59.5%), with 52 isolates (75.4%) categorized as MRSA. Of patients who received MRSA coverage, 49.4% had MRSA-negative cultures. In 31.4% of patients with positive MRSA cultures, MRSA coverage was not provided.

Patients with a positive nares swab had a 3.16 increased risk of positive MRSA wound culture compared with patients with a negative nares swab (95% CI 2.16 to 4.62; p<0.0001).

Adverse Events

N/A

Study Author Conclusions

MRSA nares swab is a more accurate predictor of MRSA wound infection compared with clinical risk factors or EM provider’s choice of antibiotics. MRSA nares swab may be a useful tool in the ED.

InpharmD Researcher Critique

Data derived from a single center and a small sample size may not be generalizable to larger patient cohorts, and of the sample, only 20.7% of patients had cellulitis; the number of patients who presented with MRSA cellulitis is unknown. Patients were screened using the ED research associate program, thus introducing sample bias. Additionally, the study did not provide an analysis on NPV specific to nares swab for MRSA cellulitis.

References:

Acquisto NM, Bodkin RP, Brown JE, et al. MRSA nares swab is a more accurate predictor of MRSA wound infection compared with clinical risk factors in emergency department patients with skin and soft tissue infections. Emerg Med J. 2018;35(6):357-360. doi:10.1136/emermed-2017-206843

 

Role of nasal swab culture in guiding antimicrobial therapy for acute cellulitis in the era of community-acquired methicillin-resistant Staphylococcus aureus: A prospective study of 89 patients

Design

Prospective observational study

N= 89

Objective

To assess whether nasal MRSA colonization predicts acute MRSA cellulitis and a delayed response to antimicrobial therapy

Study Groups

No S. aureus colonization (n= 74)

Colonized with MSSA (n= 11)

Colonized with MRSA (n= 4)

Inclusion Criteria

Adult (>20 years old) patients who visited the emergency service and received a diagnosis of acute cellulitis which required hospitalization

Exclusion Criteria

Not specified

Methods

At enrollment, all participants received a nasal swab culture to detect S. aureus carriage. A nasal swab was performed by inserting the swab tube 1 cm into the nostril, and then placing it on trypticase soy agar supplemented with 5% sheep blood which was incubated overnight at 37 C. One colony from every single culture was selected, and the identification and susceptibility testing of S. aureus was based on standard methods.

Duration

From 2013 to 2015

Outcome Measures

Primary: delayed response to therapy, as defined by (1) fever that persisted for more than 3 days under empirical antibiotics, or (2) erythema that persisted or enlarged under treatment for more than 3 days

Secondary: total duration of antibiotic use; length of hospitalization; computed tomography (CT) or magnetic resonance imaging (MRI); surgical interventions (incision, drainage, or debridement)

Baseline Characteristics

 

No S. aureus colonization (n= 74)

Colonized with MSSA (n= 11)

Colonized with MRSA (n= 4)  p-Value

Age, years (range)

52 ± 16.5 (22-89) 44 ± 15.8 (21-62) 62 ± 10.4 (50-75) 0.14

Male

51 (69%) 7 (64%) 2 (50%) 0.71

Underlying conditions

Diabetes mellitus

Gout

Hemodialysis

Prosthetic devices

Recent (3 mo) anti-MRSA agent

Recent anti-MSSA agent

Recent hospitalization

 

20 (27%)

8 (11%)

1 (1%)

2 (3%)

3 (4%)

4 (5%)

3 (4%)

 

1 (9%)

2 (18%)

0

1 (9%)

1 (9%)

1 (9%)

0

 

0

0

0

0

1 (25%)

1 (25%)

0

 

0.22

0.59

0.90

0.51

0.18

0.30

0.40

Previous MRSA colonization or infection (within 1 year)

2 (3%) 0 0 0.81

Sites of acute cellulitis

Extremities

Head or neck

Trunk

 

70 (95%)

1 (1%)

3 (4%)

 

11 (100%)

0

0

 

4 (100%)

0

0

 

0.65

0.90

0.73

Body temperature, °C

Initial temperature > 37.5 °C

37.4 ± 1.1

29 (39%)

38 ± 1.5

7 (64%)

39 ± 1.1

2 (50%)

0.07

0.17

Blood culture

S.aureus

Streptococcus

Other

 

0

1

2

 

0

0

 

0

1

0

 

-

0.007

0.81

Empiric antibiotics

Anti-MSSA

Anti-MRSA

 

70 (95%)

13 (18%)

 

11 (100%)

3 (27%)

 

4 (100%)

0

 

0.65

0.47

Results

Endpoint

No S. aureus colonization (n= 74)

Colonized with MSSA (n= 11)

Colonized with MRSA (n= 4) 

p-Value

Delayed response to antibiotic therapy

13/71 (18%) 2/11 (18%) 1/4 (25%) 0.93

Pus formation

S. aureus

MSSA

MRSA

Streptococcus

Other

No growth

17/71 (23%)

 

3 (4%)

4 (5%)

2 (3%)

3 (4%)

7 (9%)

5/11 (46%)

 

3 (27%)

0

1 (9%)

2 (18%)

0

2/4 (50%)

 

0

1 (25%)

0

0

1 (25%) 

0.17

 

0.014

0.17

0.51

0.15

0.31

Total duration of antibiotics, days (range)

17 ± 11 (1-66) 19 ± 11 (10-35) 16 ± 6.7 (12-26) 0.79

Surgical intervention

8/71 (11%) 0/11 1/4 (25%) 0.32

Duration of hospitalization, days (range)

7.6 ± 8 (0-56) 8.1 ± 6.4 (3-26) 6.5 ± 3.3 0.87

Of the 24 patients who developed purulent cellulitis, five and two patients have nasal colonization of MSSA and MRSA, respectively. MRSA growth from nasal swab culture had a sensitivity of 20% (1/5) and specificity of 95% (18/19) in predicting MRSA growth from pus culture among the 24 purulent cellulitis cases.

Adverse Events

N/A

Study Author Conclusions

Nasal MRSA carriage is highly specific in predicting community-acquired MRSA cellulitis for patients with purulent cellulitis. The high specificity of 95% may allow a recommendation of antimicrobial therapy against MRSA for acute cellulitis patients with nasal MRSA carriage as well as other risk factors of MRSA infections. Empirical anti-MRSA agents are not needed in patients without nasal MRSA colonization.

InpharmD Researcher Critique

Observational studies are prone to methodological bias and cannot prove causality. Given the small numbers of MRSA carriers (n= 4) and culture-confirmed MRSA cellulitis (n= 5), the estimates for sensitivity and specificity of using nasal MRSA carriage in predicating culture-confirmed MRSA cellulitis may not be precise. 

References:

Hsu MS, Liao CH, Fang CT. Role of nasal swab culture in guiding antimicrobial therapy for acute cellulitis in the era of community-acquired methicillin-resistant Staphylococcus aureus: A prospective study of 89 patients. J Microbiol Immunol Infect. 2019;52(3):494-497. doi:10.1016/j.jmii.2019.04.001

Methicillin-resistant Staphylococcus aureus (MRSA) screening upon inpatient hospital admission: Is there concordance between nasal swab results and samples taken from skin and soft tissue?

Design

Single-site retrospective study

N= 548

Objective

To evaluate the correlation between the nasal screening results for MRSA and culture results of wound and tissue sites 

Study Groups

Wound culture (n= 337)

Tissue cultures (n= 211)

Inclusion Criteria

Aged ≥ 18 years, had undergone nasal screening for MRSA by polymerase chain reaction (PCR) upon admission along with culture of a secondary site within 30 days of admission (wound the tissue sites)

Exclusion Criteria

Not specified 

Methods

Patients' electronic health records were reviewed retrospectively to collect demographic data, past medical history, and culture results. A wound culture was defined as a culture taken from superficial wounds such as abrasions, cuts, lacerations, ulcers, burns, or associated skin disease. Tissue culture was defined as a culture taken from a deep wound such as a surgical wound, bite wound, deep trauma, or any specimen that originated from deep tissue.

Duration

Between January 2008 and June 2015

Outcome Measures

Primary: concordance between MRSA nasal swab results and MRSA wound and tissue cultures

Baseline Characteristics

  

Total cohort (N= 548)

 

Female

105 (19.2%)  

White

Native American

Black

443 (80.8%)

44 (8.0%)

15 (2.7%) 

 

Medical history

History of smoking or COPD

Previous admission within 30 d

History of MRSA infection

Immunosuppression factor

 

284 (51.8%)

114 (20.8%)

115 (21.0%)

375 (68.4%)

 
Previous diagnosis of MRSA colonization or infection 

21%

 

COPD, chronic obstructive pulmonary disease; MRSA, methicillin-resistant Staphylococcus aureus.

Results

Endpoint, % (95% CI)

Wound (n= 337)

Tissue (n= 211)

Prevalence

14.2 (10.5 to 17.9)

15.2 (10.4 to 15.3)

Sensitivity

64.6 (50.4 to 76.6) 65.5 (48.2 to 79.7)

Specificity

86.2 (81.7 to 89.7) 88.8 (83.3 to 92.7)

PPV

43.7 (32.1 to 55.3) 51.2 (35.9 to 66.5)

NPV

93.6 (90.7 to 96.5) 93.5 (89.8 to 97.2) 

In total, 71 veterans (21.1%) in the wound-culture group and 41 (19.4%) in the tissue-culture group had a positive nasal swab for MRSA. Furthermore, 31 (9.2%) had both a nasal screening positive for MRSA and a wound culture positive for MRSA, whereas 21 (10.0%) had both a nasal screening positive for MRSA and a tissue culture positive for MRSA. 

Linear regression model for medical history variables demonstrated history of MRSA colonization or infection were significant predictors of positive MRSA tests from both the nasal and tissue cultures (p< 0.05). 

CI, confidence interval; PPV, positive predictive value; NPV, negative predictive value.

Adverse Events

N/A

Study Author Conclusions

In cases of wound or tissue samples for which culture results are pending, a negative MRSA nasal swab may be a component of the decision to withhold or discontinue MRSA-active agents.

InpharmD Researcher Critique

The study is limited by its retrospective, single-center design and may not be applicable to other settings with different MRSA prevalence. Regardless, negative MRSA nasal swabs appeared to be a valuable tool for antimicrobial stewardship. 

References:

Petry NJ, Montgomery AD, Hammer KDP, Lo TS. Methicillin-resistant Staphylococcus aureus (MRSA) screening upon inpatient hospital admission: Is there concordance between nasal swab results and samples taken from skin and soft tissue?. Infect Control Hosp Epidemiol. 2020;41(11):1298-1301. doi:10.1017/ice.2020.345

 

Assessing the predictive value of methicillin-resistant Staphylococcus aureus nares colonization amongst transplant recipients and patients with neutropenia

Design

Retrospective, multicenter, observational, cohort study

N= 686,174

Objective

To assess the predictive value of methicillin-resistant Staphylococcus aureus (MRSA) nares amongst high-risk individuals, including patients with neutropenia, hematopoietic stem cell transplant (HSCT) recipients, and solid organ transplant (SOT) recipients

Study Groups

Full cohort (N= 686,174)

Neutropenic patients (n= 2,419)

Transplant recipients (n= 19,909)

Inclusion Criteria

Age ≥18 years, screened for MRSA nares colonization, included high-risk patient populations diagnosed with neutropenia (absolute neutrophil count [ANC] <1500 cells/μL) or transplant recipients (hematopoietic stem cells, pancreas, lungs, liver, kidney, intestine, and heart)

Exclusion Criteria

Not disclosed

Methods

Data collected from all Veterans Affairs sites included date of birth, sex, race, hospital admission dates, ANC, international classifications of disease codes, and positive microbiological cultures within 28 days of MRSA nares colonization assessment. MRSA nares colonization was assessed using culture and polymerase chain reaction (PCR) testing; PCR was utilized to determine predictive performance. Multiple culture sites were tested, including wound, urinary, blood, intra-abdominal, pulmonary, graft, and more.

Duration

Between January 2007 to January 2023

Outcome Measures

Primary: Predictive value of MRSA nares colonization assessed via sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) for all high-risk patients including those with neutropenia and transplant (HSCT and SOT) recipients within 28 days of first positive culture 

Baseline Characteristics

 

Full cohort

(N= 686,174)

 

 

Age, years

68.7 ± 12    

Female

24,948 (95.5%)

   

Race

White

African American

Native Hawaiian or Pacific Islander

American Indian or Alaska Native

Asian

Unknown

Declined to answer

 

403,940 (72.3%)

111,158 (19.9%)

4,961 (0.9%)

4,916 (0.9%)

2,208 (0.4%)

10,461 (1.9%)

21,031 (3.7%)

   
 

Total MRSA tests collected*

MRSA Positive Result  

MRSA test 

Culture

PCR

 

2,569,454 (40.9%)

3,707,983 (59.1%)

 

11.4%

14.3%

 

*A total of 6,277,437 tests were performed during MRSA nares colonization screening

Results

Endpoint

Full cohort 

(N= 686,174)

Neutropenic patients

(n= 2,419)

Transplant recipients

(n= 19,909)

Sensitivity

66.6% 72.4% 71.6%

Specificity

81.6% 88.9% 87.9%

PPV

27.8% 30.9% 31.8%

NPV

95.8% 97.9% 97.5%

All anatomical culture sites were included for NPV analysis. There were no significant differences in NPV of MRSA infections between culture sites. 

Adverse Events

Not disclosed

Study Author Conclusions

MRSA nares screening can reliably be used for de-escalation of anti-MRSA therapy within 28 days of bacterial culture for all patients, including solid organ and hematopoietic transplant recipients and patients with neutropenia.

InpharmD Researcher Critique

This study primarily focused on the NPV of MRSA nares screening in high-risk patient populations for avoiding or de-escalating empiric anti-MRSA treatment and assessing the NPV on the development of other multi-drug resistant organisms. Multiple anatomical culture sites were included in this study, which strengthens the evidence of NPV for MRSA nares colonization being effective as a screening tool. However, as these patient populations are at a higher risk for opportunistic infections than the general population, this study likely underestimates the applicability of NPV of MRSA nares screening. 

References:

Shaw R, Zander A, Ronnie T, et al. Assessing the predictive value of methicillin-resistant Staphylococcus aureus nares colonization amongst transplant recipients and patients with neutropenia. Open Forum Infectious Diseases. 2024;ofae408. doi:10.1093/ofid/ofae408