Controlling Transmission of Healthcare Acquired Methicillin-Resistant Staphylococcus Aureus (HA-MRSA) Infections
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This document discusses the strategies to control the transmission of healthcare acquired methicillin-resistant Staphylococcus aureus (HA-MRSA) infections in hospital settings. It includes a research question, background information, literature review, methods, and risk communication. The document emphasizes the importance of good practices, comparison of strategies, and outcomes in curbing HA complications by MRSA.
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ENVIRONMENTAL EPIDEMIOLOGY
1. Research (PICO) question
1. Research (PICO) question
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Can transmission of healthcare acquired methicillin-resistant
Staphylococcus aureus (HA-MRSA) be controlled by multiple
interventions?
P (population) - patients and nursing staffs
I (intervention) – Addressing the need to tackle transmission of methicillin-
resistant Staphylococcus aureus (MRSA) in hospital settings and examine the
good practices
C (comparison) – various strategies to minimise the acquisitions of MRSA
O (outcome) – curbing healthcare acquired (HA) complications by MRSA.
2. Background
i. Literature review
The review of several literatures was conducted utilising the search databases
such as CINAHL, PubMed and EBSCOhost, Additionally the search items
include methicillin-resistant Staphylococcus aureus, control of infection by
MRSA and implementation of control measures for patients and nurses. The
literature search consisted of 53 articles out of which 20 were chosen to identify
the problems, notification on hazard, response to dose, exposure assessment and
characterize the risk.
Globally, healthcare acquired infections are one of the major implications of
mortality. Morbidity and excessive financial burden. Staphylococcus aureus is
most potent nosocomial pathogen leading to healthcare acquired complications
such as pneumonia, meningitis and bacteraemia. The administration of
antibiotics and antimicrobial agents has significantly increased in the recent
past; as a result, there has been a drastic reduction in infection and death rates
(Littman and Viens, 2015). As antibiotics have been the major line of treatment
for a long period, few bacteria have developed resistance towards the antibiotics
thereby rendering the treatment ineffective (Lloyd et al., 2005). Currently,
antibiotic resistance has become a problem worldwide and research is being
done to curb antibiotic resistance (Fukunaga et al., 2016). As such, MRSA, a
strain of S. aureus exhibits resistance against methicillin and is a serious
concern to public health owing to its elevated levels in mortality rates among
the antibiotic resistant organisms.
Staphylococcus aureus (HA-MRSA) be controlled by multiple
interventions?
P (population) - patients and nursing staffs
I (intervention) – Addressing the need to tackle transmission of methicillin-
resistant Staphylococcus aureus (MRSA) in hospital settings and examine the
good practices
C (comparison) – various strategies to minimise the acquisitions of MRSA
O (outcome) – curbing healthcare acquired (HA) complications by MRSA.
2. Background
i. Literature review
The review of several literatures was conducted utilising the search databases
such as CINAHL, PubMed and EBSCOhost, Additionally the search items
include methicillin-resistant Staphylococcus aureus, control of infection by
MRSA and implementation of control measures for patients and nurses. The
literature search consisted of 53 articles out of which 20 were chosen to identify
the problems, notification on hazard, response to dose, exposure assessment and
characterize the risk.
Globally, healthcare acquired infections are one of the major implications of
mortality. Morbidity and excessive financial burden. Staphylococcus aureus is
most potent nosocomial pathogen leading to healthcare acquired complications
such as pneumonia, meningitis and bacteraemia. The administration of
antibiotics and antimicrobial agents has significantly increased in the recent
past; as a result, there has been a drastic reduction in infection and death rates
(Littman and Viens, 2015). As antibiotics have been the major line of treatment
for a long period, few bacteria have developed resistance towards the antibiotics
thereby rendering the treatment ineffective (Lloyd et al., 2005). Currently,
antibiotic resistance has become a problem worldwide and research is being
done to curb antibiotic resistance (Fukunaga et al., 2016). As such, MRSA, a
strain of S. aureus exhibits resistance against methicillin and is a serious
concern to public health owing to its elevated levels in mortality rates among
the antibiotic resistant organisms.
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MRSA or Methicillin-resistant Staphylococcus aureus has its effect in precisely
the similar manner as that of Staphylococcus aureus and leads the exact manner
of infections and sufferings (Lee et al., 2018). MRSA is different from the other
is because of its resistance to some antibiotics. There are various antibiotics
which are effective in such infections but it may be a bit risky to use as it might
have chances to cause severe side effects (Turner et al., 2019). Though,
development of the MRSA infection is very not as much common as for normal
people, but it is more frequent for the individuals who obtain Methicillin-
resistant Staphylococcus aureus to be transporters (Harkins et al., 2017). These
people are often called as ‘colonised’ people, which states that the organism
exists without harming the individual, on their skin or in their nasal region or
throat, and are found to be not cause any difficulties related to health. one of the
amendments that has been made by the legal agencies is patient advocacy in
condition of Methicillin-resistant Staphylococcus aureus infection (Galar et al.,
2019). Patient advocacy provides the right to the person take his/her health care
related as well as treatment related decision and if not possible they can hire
their personal advocates.
Patient advocacy and Personal advocacy is permitted to patients admitted to
health care settings which are licensed under the chapter 405. The legal
amendment states that the patient has total right to choose personal advocate
and the advocate must be with the patient in every process of the examination,
treatment and effective result while suffering from infection due to Methicillin-
resistant Staphylococcus aureus (Werner & Shaban, 2018). The patients have
the authority to recruit more than one personal advocate for themselves. The
patient advocates role is to help the patient make effective decisions regarding
the health, treatment and recovery. The healthcare has the right to limit the
advocates presence in areas where it may risk the patient’s health such as sterile
chambers prepared for the patient as Methicillin-resistant Staphylococcus
aureus has the high chance of spreading. In any circumstance, if the patient
advocate is not permitted to stay with the patient, the health care setting is
bound to provide a written application with detailed reason behind not
permitting the advocate (Walrath et al., 2015). The copies should be provided to
the patient as well as the advocate. It is necessary for the patient as well as the
nursing staff to practice protective measures in order to avoid the spread of the
infection (Werner, Zimmerman & Elder, 2016). The nursing staff needs to
follow basic rules such as keeping the patient in a separate chamber that needs
to be sterile enough to avoid the infection to grow or spread. The nurses at the
same point needs to preserve them from getting infected thus they need to use
the similar manner as that of Staphylococcus aureus and leads the exact manner
of infections and sufferings (Lee et al., 2018). MRSA is different from the other
is because of its resistance to some antibiotics. There are various antibiotics
which are effective in such infections but it may be a bit risky to use as it might
have chances to cause severe side effects (Turner et al., 2019). Though,
development of the MRSA infection is very not as much common as for normal
people, but it is more frequent for the individuals who obtain Methicillin-
resistant Staphylococcus aureus to be transporters (Harkins et al., 2017). These
people are often called as ‘colonised’ people, which states that the organism
exists without harming the individual, on their skin or in their nasal region or
throat, and are found to be not cause any difficulties related to health. one of the
amendments that has been made by the legal agencies is patient advocacy in
condition of Methicillin-resistant Staphylococcus aureus infection (Galar et al.,
2019). Patient advocacy provides the right to the person take his/her health care
related as well as treatment related decision and if not possible they can hire
their personal advocates.
Patient advocacy and Personal advocacy is permitted to patients admitted to
health care settings which are licensed under the chapter 405. The legal
amendment states that the patient has total right to choose personal advocate
and the advocate must be with the patient in every process of the examination,
treatment and effective result while suffering from infection due to Methicillin-
resistant Staphylococcus aureus (Werner & Shaban, 2018). The patients have
the authority to recruit more than one personal advocate for themselves. The
patient advocates role is to help the patient make effective decisions regarding
the health, treatment and recovery. The healthcare has the right to limit the
advocates presence in areas where it may risk the patient’s health such as sterile
chambers prepared for the patient as Methicillin-resistant Staphylococcus
aureus has the high chance of spreading. In any circumstance, if the patient
advocate is not permitted to stay with the patient, the health care setting is
bound to provide a written application with detailed reason behind not
permitting the advocate (Walrath et al., 2015). The copies should be provided to
the patient as well as the advocate. It is necessary for the patient as well as the
nursing staff to practice protective measures in order to avoid the spread of the
infection (Werner, Zimmerman & Elder, 2016). The nursing staff needs to
follow basic rules such as keeping the patient in a separate chamber that needs
to be sterile enough to avoid the infection to grow or spread. The nurses at the
same point needs to preserve them from getting infected thus they need to use
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protections such as gloves, protective aprons, hand hygiene and other cleaning
and disinfecting measures (Garvey et al., 2019).
ii. Rational and significance:
One of the studies revealed that the risk of mortality was twice higher than that
of methicillin-sensitive S. aureus which significantly increases the duration of
stay, utilizing resources of the healthcare facilities, medication and extra nursing
staffs for care thus leading to economic burden for the patient (Kundrapu et al.,
2012). MRSA can survive on hospital surfaces such as catheters, surgical
instruments, hospital floor and furniture and cause outbreaks if left
uncontrolled. Consequently, it is important to understand the disease burden and
the potential factors associated with the spread of infection in order to manage
HA-MRSA (Fox et al., 2015). Furthermore, identifying the risk factors will
ensure formulation of guidelines and recommendations for prevention policies,
in particular, good hand hygiene, adequate care of vascular devices and
cleanliness of the hospital environment (Minhas et al., 2011).
iii. Biological plausibility:
The biological plausibility includes prolonged bacteraemia resulting in severe
complications such as meningitis and septic shock. In addition, these
complications result in prolonged bacteraemia (Green, 2015). In addition,
MRSA based interventions have a significant impact in surgery, for instance
mupirocin administered intranasally has significantly minimised MRSA
associated infections at the site of surgery in orthopaedic and cardiothoracic
surgery, however not effective in general surgery. The causes for such reasons
remain unclear, however a dosage regimen to decolonise MRSA prior to
surgery and development of rapid diagnostic assays can be effective to curb
MRSA transmission. Also, utilisation of two interventions such as hygiene and
antibiotics or placement of patients in isolation rooms or proper screening can
be effective in the prevention and control.
and disinfecting measures (Garvey et al., 2019).
ii. Rational and significance:
One of the studies revealed that the risk of mortality was twice higher than that
of methicillin-sensitive S. aureus which significantly increases the duration of
stay, utilizing resources of the healthcare facilities, medication and extra nursing
staffs for care thus leading to economic burden for the patient (Kundrapu et al.,
2012). MRSA can survive on hospital surfaces such as catheters, surgical
instruments, hospital floor and furniture and cause outbreaks if left
uncontrolled. Consequently, it is important to understand the disease burden and
the potential factors associated with the spread of infection in order to manage
HA-MRSA (Fox et al., 2015). Furthermore, identifying the risk factors will
ensure formulation of guidelines and recommendations for prevention policies,
in particular, good hand hygiene, adequate care of vascular devices and
cleanliness of the hospital environment (Minhas et al., 2011).
iii. Biological plausibility:
The biological plausibility includes prolonged bacteraemia resulting in severe
complications such as meningitis and septic shock. In addition, these
complications result in prolonged bacteraemia (Green, 2015). In addition,
MRSA based interventions have a significant impact in surgery, for instance
mupirocin administered intranasally has significantly minimised MRSA
associated infections at the site of surgery in orthopaedic and cardiothoracic
surgery, however not effective in general surgery. The causes for such reasons
remain unclear, however a dosage regimen to decolonise MRSA prior to
surgery and development of rapid diagnostic assays can be effective to curb
MRSA transmission. Also, utilisation of two interventions such as hygiene and
antibiotics or placement of patients in isolation rooms or proper screening can
be effective in the prevention and control.
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3. Methods
i. Problem identification
The chances of acquiring MRSA at healthcare increase with immunocompetent
and immune susceptible patients, elderly, recipients of organ transplant, cancer
patients with prolonged chemotherapy, diabetics, chronic diseases, steroid
therapy, intravenous drug users, and those with prolonged medication with
antibiotics. The Centre for Disease Control states the 5 C’s such as crowding,
skin-skin contact especially between patients, their family members and nursing
staffs in the hospital settings, compromised skin, contamination and lack of
cleanliness as the prime factors for transmission of MRSA. In addition, patients
with previous colonisation with the strain, indwelling devices such as prolonged
vascular access, urinary catheter, endoscopic gastrostomy and drains in wound
(Bode et al., 2010). Furthermore, chronic wounds and admission in high risk
areas in the hospitals such as intensive critical care unit and burns may also be a
major risk problem with MRSA (Haverstick et al., 2017).
One of the studies conducted by Fox et al. (2015) assessed the rate of MRSA
associated hospital infections such as urinary tract infection due to in-dwellers
and central line associated systemic infection over a period of twelve months.
The study was based on a cardiovascular intensive care unit which is considered
a high-risk area where 1 nurse took care of 2 patients. A protocol for hand
hygiene was followed in the premises by patients that were admitted in addition
the nursing staffs of that unit. The intervention consisted of wiping the hand of
patients thrice a day using the wipes containing the disinfectant chlorohexidine
gluconate (2%) and the medial report was noted down. Results revealed a
reduction in the mean monthly rate of catheter associated urinary tract infection
from 9.1 to 5.6 in one thousand catheter days and a reduction from 1 to 0.50 in
one thousand catheter days for central line associated bloodstream infections.
These results indicated that following the protocol for hand hygiene
significantly reduced MRSA associated hospital infections than the results
obtained prior to the twelve-month period (Fox et al., 2015).
In another study, assessment of providing health education to patients, nursing
staffs and usage of hand hygiene protocol was performed to minimise MRSA
transmission via increased usage of hand hygiene protocol and educating the
patients to utilise hand hygiene wipes. This study was conducted for over a 19-
i. Problem identification
The chances of acquiring MRSA at healthcare increase with immunocompetent
and immune susceptible patients, elderly, recipients of organ transplant, cancer
patients with prolonged chemotherapy, diabetics, chronic diseases, steroid
therapy, intravenous drug users, and those with prolonged medication with
antibiotics. The Centre for Disease Control states the 5 C’s such as crowding,
skin-skin contact especially between patients, their family members and nursing
staffs in the hospital settings, compromised skin, contamination and lack of
cleanliness as the prime factors for transmission of MRSA. In addition, patients
with previous colonisation with the strain, indwelling devices such as prolonged
vascular access, urinary catheter, endoscopic gastrostomy and drains in wound
(Bode et al., 2010). Furthermore, chronic wounds and admission in high risk
areas in the hospitals such as intensive critical care unit and burns may also be a
major risk problem with MRSA (Haverstick et al., 2017).
One of the studies conducted by Fox et al. (2015) assessed the rate of MRSA
associated hospital infections such as urinary tract infection due to in-dwellers
and central line associated systemic infection over a period of twelve months.
The study was based on a cardiovascular intensive care unit which is considered
a high-risk area where 1 nurse took care of 2 patients. A protocol for hand
hygiene was followed in the premises by patients that were admitted in addition
the nursing staffs of that unit. The intervention consisted of wiping the hand of
patients thrice a day using the wipes containing the disinfectant chlorohexidine
gluconate (2%) and the medial report was noted down. Results revealed a
reduction in the mean monthly rate of catheter associated urinary tract infection
from 9.1 to 5.6 in one thousand catheter days and a reduction from 1 to 0.50 in
one thousand catheter days for central line associated bloodstream infections.
These results indicated that following the protocol for hand hygiene
significantly reduced MRSA associated hospital infections than the results
obtained prior to the twelve-month period (Fox et al., 2015).
In another study, assessment of providing health education to patients, nursing
staffs and usage of hand hygiene protocol was performed to minimise MRSA
transmission via increased usage of hand hygiene protocol and educating the
patients to utilise hand hygiene wipes. This study was conducted for over a 19-

month period and results indicated that the rates for MRSA drastically reduced
by 63% post-intervention (Strigley et al., 2016).
ii. Hazard notification:
In cases where the laboratory in the healthcare facility confirms MRSA that has
been isolated from a patient who is admitted in the hospital, the person in-
charge, either the general practitioner, coordinator of infection control, the
nursing staffs who take care of that patient or the unit and personnel who are
recommended as per the guidelines of the healthcare facilities (Peters et al.,
2017). In case the notification of hazard occurred after the working hours of the
unit responsible for infection control and prevention, there must be a system to
ensure the notification is conveyed to the personnel in the unit at the earliest.
However, the duty nurse can be informed in such scenario.
iii. Dose response:
Vancomycin hydrochloride is considered as the gold standard for treating
MRSA associated infections. However new antibiotics such as dalfopristin,
linezolid and tigecycline are mentioned to have delirious effects on MRSA (Lee
et al., 2013), however they are expensive and not much of clinical research has
been done. In addition, sub-minimum inhibitory concentration of beta-lactam
antibiotics induced biofilm formation and the dose response was not effective.
iv. Exposure assessment:
MRSA assessment is based on the results of culture and system to screen
patients with confirmed history for MRSA. Clinical isolates from MRSA
infected patients must be the major component for management of surveillance
within the healthcare settings (Currie et al., 2013). Facilities that follow strict
surveillance program can identify the reservoirs or carriers of MRSA. It is
mandatory for exposure assessment to track patients who are positive for
MRSA via screening based on location, patient proportion and service provide
clinically. The data should be consistent for the evaluation to be relevant and
appropriate and comparative for studies prior and after therapy (Mishal et al.,
2001). The prevalence of MRSA is the ratio of the patients who colonize and
by 63% post-intervention (Strigley et al., 2016).
ii. Hazard notification:
In cases where the laboratory in the healthcare facility confirms MRSA that has
been isolated from a patient who is admitted in the hospital, the person in-
charge, either the general practitioner, coordinator of infection control, the
nursing staffs who take care of that patient or the unit and personnel who are
recommended as per the guidelines of the healthcare facilities (Peters et al.,
2017). In case the notification of hazard occurred after the working hours of the
unit responsible for infection control and prevention, there must be a system to
ensure the notification is conveyed to the personnel in the unit at the earliest.
However, the duty nurse can be informed in such scenario.
iii. Dose response:
Vancomycin hydrochloride is considered as the gold standard for treating
MRSA associated infections. However new antibiotics such as dalfopristin,
linezolid and tigecycline are mentioned to have delirious effects on MRSA (Lee
et al., 2013), however they are expensive and not much of clinical research has
been done. In addition, sub-minimum inhibitory concentration of beta-lactam
antibiotics induced biofilm formation and the dose response was not effective.
iv. Exposure assessment:
MRSA assessment is based on the results of culture and system to screen
patients with confirmed history for MRSA. Clinical isolates from MRSA
infected patients must be the major component for management of surveillance
within the healthcare settings (Currie et al., 2013). Facilities that follow strict
surveillance program can identify the reservoirs or carriers of MRSA. It is
mandatory for exposure assessment to track patients who are positive for
MRSA via screening based on location, patient proportion and service provide
clinically. The data should be consistent for the evaluation to be relevant and
appropriate and comparative for studies prior and after therapy (Mishal et al.,
2001). The prevalence of MRSA is the ratio of the patients who colonize and

are infected with MRSA and the number of patients in the population study at
one point of time. In addition, the exposure assessment should possess
definitions for all the measurements. Acquisition of the infection is related to
hospitalization if MRSA infection is detected more than 2 days following
admission (Borg et al., 2012).
At hospitals it is important to follow and notify the rates of prevalence for every
high-risk unit (Dickmann et al., 2017). It is important to identify populations
and service lines at high risk, analyse the transmission of MRSA in the
population of patients over a period of time before and after the interventions,
compare the spread of MRSA to evaluate whether multiple interventions are
necessary, prioritise interventions for specific patient care units and among
specific populations and develop a dosage regimen and effectively
communicate to the nursing staffs. One of the evaluations for the exposure
assessment of MRSA is determined as follows:
No. of new MRSA cases per unit per month/no. of patient days * 1000 = HA-
MRSA rates per 1000unit patient days
4. Risk communication:
The communication of risks involves several approaches to reduce the spread of
MRSA in healthcare settings such as wiping the hands regularly to minimise
infection and carriage. Contamination of the hand of healthcare staffs is one of
the major reasons for the transmission of MRSA among patients. Hand gloves,
instruments and aprons utilised by the healthcare workers may be the source of
infection. One of the studies conducted by Boyce et al (1997) revealed that 42%
of the gloves used by the nurse are contaminated however they had no direct
contact with the MRSA infected patients but experienced contact with the
surface of the room where the patients were admitted.
The clothing of the nurses is considered as one of the factors for transmission
among patients. Instruments utilised in the patient’s care such as thermometers,
blood pressure monitoring devices and otoscopes act as agents for the spread of
infection (Schoeder A et al., 2015). In addition, the use of antibiotics is
considered a risk communication factor. Furthermore, most of the complaints
from patients and their family members include improper communication about
MRSA. The groups for patient advocacy have given importance for rapid and
increased information on MRSA in hospital settings (Gigerenzer and Werwerth,
2013). This communication strategy will assist in clinical governance and
one point of time. In addition, the exposure assessment should possess
definitions for all the measurements. Acquisition of the infection is related to
hospitalization if MRSA infection is detected more than 2 days following
admission (Borg et al., 2012).
At hospitals it is important to follow and notify the rates of prevalence for every
high-risk unit (Dickmann et al., 2017). It is important to identify populations
and service lines at high risk, analyse the transmission of MRSA in the
population of patients over a period of time before and after the interventions,
compare the spread of MRSA to evaluate whether multiple interventions are
necessary, prioritise interventions for specific patient care units and among
specific populations and develop a dosage regimen and effectively
communicate to the nursing staffs. One of the evaluations for the exposure
assessment of MRSA is determined as follows:
No. of new MRSA cases per unit per month/no. of patient days * 1000 = HA-
MRSA rates per 1000unit patient days
4. Risk communication:
The communication of risks involves several approaches to reduce the spread of
MRSA in healthcare settings such as wiping the hands regularly to minimise
infection and carriage. Contamination of the hand of healthcare staffs is one of
the major reasons for the transmission of MRSA among patients. Hand gloves,
instruments and aprons utilised by the healthcare workers may be the source of
infection. One of the studies conducted by Boyce et al (1997) revealed that 42%
of the gloves used by the nurse are contaminated however they had no direct
contact with the MRSA infected patients but experienced contact with the
surface of the room where the patients were admitted.
The clothing of the nurses is considered as one of the factors for transmission
among patients. Instruments utilised in the patient’s care such as thermometers,
blood pressure monitoring devices and otoscopes act as agents for the spread of
infection (Schoeder A et al., 2015). In addition, the use of antibiotics is
considered a risk communication factor. Furthermore, most of the complaints
from patients and their family members include improper communication about
MRSA. The groups for patient advocacy have given importance for rapid and
increased information on MRSA in hospital settings (Gigerenzer and Werwerth,
2013). This communication strategy will assist in clinical governance and
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adhering to professional and ethical guidelines as per the national and hospital
guidelines. Proper education to the patients will ensure the patients informing
about the requirement for screening and subsequent entry for admission in the
hospital. Furthermore, sharing of information and hand hygiene can reduce the
transmission of MRSA. Lack of knowledge about informing the status of
MRSA is one of the barriers that result in the spread of infection (Fukunaga et
al., 2017). In addition, the process of documentation must be made simple and
the feedback from audits on the patient proportions have to be recorded. Also,
the patient’s MRSA-positive status should be notified to the new healthcare
settings where the patients were to be transferred. Collaboration with nursing
staffs, planning in the discharge and management of patient’s case are effective
measures. In addition, it is essential to develop a transfer tool that is like the tool
developed by the Centre for Disease Control.
Major findings in the developing strategies are:
i) hand hygiene with chlorhexidine significantly reduced the acquisition of
MRSA and systemic infections (Climno et al., 2013)
ii) information about screening and outcomes to the patient
iii) disinfection of touch surfaces in patient’s rooms infected with MRSA
significantly minimised the transmission of infection via hands of nursing staffs
and other healthcare workers who took care of the patients.
iv) patients with positive MRSA can have recurrent infections due to drug
resistance, prolongEd admission in hospitals and be a carrier for MRSA
(Littman and Viens, 2015).
v) Isolation of contact and deceased patients from other patients in the unit and
nurses.
5. Conclusion:
The healthcare workers, nurses who work in accordance with the patients
infected with MRSA must abide by the guidelines and implement effective
strategies to prevent the transmission of MRSA within the healthcare settings.
In addition, education about MRSA to patients, prompt techniques of
disinfection can effectively prevent and control MRSA transmission.
Consequently, multiple interventions can promote effective management of
MRSA in hospitals. This will prevent prolonged stays in the hospital, charges
that cannot be reimbursed from Medicare and Medicaid and ensure reduction in
the financial burden of the patient.
6. References
guidelines. Proper education to the patients will ensure the patients informing
about the requirement for screening and subsequent entry for admission in the
hospital. Furthermore, sharing of information and hand hygiene can reduce the
transmission of MRSA. Lack of knowledge about informing the status of
MRSA is one of the barriers that result in the spread of infection (Fukunaga et
al., 2017). In addition, the process of documentation must be made simple and
the feedback from audits on the patient proportions have to be recorded. Also,
the patient’s MRSA-positive status should be notified to the new healthcare
settings where the patients were to be transferred. Collaboration with nursing
staffs, planning in the discharge and management of patient’s case are effective
measures. In addition, it is essential to develop a transfer tool that is like the tool
developed by the Centre for Disease Control.
Major findings in the developing strategies are:
i) hand hygiene with chlorhexidine significantly reduced the acquisition of
MRSA and systemic infections (Climno et al., 2013)
ii) information about screening and outcomes to the patient
iii) disinfection of touch surfaces in patient’s rooms infected with MRSA
significantly minimised the transmission of infection via hands of nursing staffs
and other healthcare workers who took care of the patients.
iv) patients with positive MRSA can have recurrent infections due to drug
resistance, prolongEd admission in hospitals and be a carrier for MRSA
(Littman and Viens, 2015).
v) Isolation of contact and deceased patients from other patients in the unit and
nurses.
5. Conclusion:
The healthcare workers, nurses who work in accordance with the patients
infected with MRSA must abide by the guidelines and implement effective
strategies to prevent the transmission of MRSA within the healthcare settings.
In addition, education about MRSA to patients, prompt techniques of
disinfection can effectively prevent and control MRSA transmission.
Consequently, multiple interventions can promote effective management of
MRSA in hospitals. This will prevent prolonged stays in the hospital, charges
that cannot be reimbursed from Medicare and Medicaid and ensure reduction in
the financial burden of the patient.
6. References
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Fox C., Wavra T., Drake D., Mulligan D., Bennett Y., Nelson C., Kirkwood P.,
Jones L., Bader M. (2015). Use of a patient hand hygiene protocol to reduce
hospital acquired infections and improve nurses hand washing. American
Journal of Critical Care. Vol 24 (3). 217-223.
Strigley J. A., Furness C. D., Gardam M. (2016). Interventions to improve
patient hand hygiene: a systematic review. Journal of Hospital Infection. Vol 94
(1). 23-29
Haverstick S., Goodrich C., Freeman R., James S., Kullar R., Ahrens M. (2017).
Patient’s hand washing and reducing hospital acquired infection. Critical Care
Nurse. Vol 37 (3).
Climno M. W., Yokoe D. S., Warren D. K., Perl T. M., Bolon M., Herwaldt
L.A., Wong E. S. (2013). Effect of daily chlorohexidine bathing on hospital-
acquired infection. N Engl J Med. Vol 368. 533-542
Currie K., Knussen C., Price L., Reilly J. (2013). Methicillin-resistant
Staphylococcus aureus screening aas a patient safety initiative using patients
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contamination of healthcare workers hands. Infect Control Hosp Epidemiology.
Vol 33 (10). 1039-1042
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Risk factors for positive admission surveillance cultures for methicillin resistant
Staphylococcis aureus and vancomycin-resistant eneterococci in neurocritical
care unit. Critical care Med. Vol 39. 2322-2329
Mishal J., Sherer Y., Levin Y., Katz D., Embon E. (2001). Two stage evaluation
and intravention program for control of methicillin resistant Staphylococcus
aureus in the hospital setting. Scandinavian Journal of Infectious Diseases. Vol
33 (7). 498-501
Schroeder A., Schroeder M. A., D’Amico F (2009). What’s growing on your
stethoscope? And what you can do about it. J Fam Pract. Vol 58. 408-409
Dickmann P et al. (2017). Communicating the risk of MRSA: the role of
clinical practice, regulation and other policies in five European countries.
Frontiers in Public Health. Vol 5 (44). Doi: 10.3389/fpubh.2017/00044
Jones L., Bader M. (2015). Use of a patient hand hygiene protocol to reduce
hospital acquired infections and improve nurses hand washing. American
Journal of Critical Care. Vol 24 (3). 217-223.
Strigley J. A., Furness C. D., Gardam M. (2016). Interventions to improve
patient hand hygiene: a systematic review. Journal of Hospital Infection. Vol 94
(1). 23-29
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Patient’s hand washing and reducing hospital acquired infection. Critical Care
Nurse. Vol 37 (3).
Climno M. W., Yokoe D. S., Warren D. K., Perl T. M., Bolon M., Herwaldt
L.A., Wong E. S. (2013). Effect of daily chlorohexidine bathing on hospital-
acquired infection. N Engl J Med. Vol 368. 533-542
Currie K., Knussen C., Price L., Reilly J. (2013). Methicillin-resistant
Staphylococcus aureus screening aas a patient safety initiative using patients
experiences to improve the quality of screening practices. Journal of Clinical
Nursing. Doi: 10.111/joen.12386
Kundrapu s., Sunkesula V., Jury I. A., Sitzlar B. M., Donskey C. J. (2012).
Daily disinfection of high touch surfaces in isolation rooms to reduce
contamination of healthcare workers hands. Infect Control Hosp Epidemiology.
Vol 33 (10). 1039-1042
Minhas P., Perl T. M., Carroll K. C., Shepard J. W., Shagraw K. A et al (2011).
Risk factors for positive admission surveillance cultures for methicillin resistant
Staphylococcis aureus and vancomycin-resistant eneterococci in neurocritical
care unit. Critical care Med. Vol 39. 2322-2329
Mishal J., Sherer Y., Levin Y., Katz D., Embon E. (2001). Two stage evaluation
and intravention program for control of methicillin resistant Staphylococcus
aureus in the hospital setting. Scandinavian Journal of Infectious Diseases. Vol
33 (7). 498-501
Schroeder A., Schroeder M. A., D’Amico F (2009). What’s growing on your
stethoscope? And what you can do about it. J Fam Pract. Vol 58. 408-409
Dickmann P et al. (2017). Communicating the risk of MRSA: the role of
clinical practice, regulation and other policies in five European countries.
Frontiers in Public Health. Vol 5 (44). Doi: 10.3389/fpubh.2017/00044

Lee et al. (2013). Comparison of strategies to reduce methicillin resistant
Staphylococcus aureus rates in surgical patients: a controlled multicentre
intervention trial. Infectious Diseases. Vol 3 (9).
Green B. N. (2012). Methicillin resistant Staphylococcus aureus: an overview
for manual therapists. J Chirop Med. Vol 11 (1), 64-75
Gigerenzer G., Wegwarth O. (2013). Five-year survival rates can mislead. BMJ.
Vol 348
Borg M. A., Camilleri L., Waisfisz B. (2012). Understanding the epidemiology
of MRSA in Europe: do we need to think outside the box? J Hosp Infect. Vol 81
(4). 251-256
Lloyd S. J. O., Svhreiber S. J., Kopp P. E et al. (2005). Superspreading and the
effect of individual variation on disease emergence. Nature. Vol 438. 355-359
Bode L. G., Kloytmans J .A., Wertherirn H. F. et al. (2010). Preventing surgical
site infections in nasal carriers of Staphylococcus aureus. N Eng J Med. 2010.
Vol 362. 9-17.
Fukunaga B. T., Sumida W. K., Taira D. A., Davis J. W., Seto T. B. (2016).
Hospital acquired methicillin resistant Staphylococcus aureus bacteremia
related to Medicare antibiotic prescriptions: a state level analysis. Hawaii J Med
Public Health. Vol 75 (10). 303-309
Littman J., Viens A. M. (2015). The ethical significance of antimicrobial
resistance. Public Health Ethics. Vol 8 (3). 209-224.
Peters C., Dulon M., Kleimuller O., Nienhaus A., Schabion A. (2017). MRSA
prevalence and risk factors among health personnel and residents in nursing
homes in Hamburg, Germany-a cross sectional study. PLoS One. Vol 12 (1).
E0169425
Galar, A., Weil, A. A., Dudzinski, D. M., Muñoz, P., & Siedner, M. J. (2019).
Methicillin-Resistant Staphylococcus aureus Prosthetic Valve Endocarditis:
Pathophysiology, Epidemiology, Clinical Presentation, Diagnosis, and
Management. Clinical microbiology reviews, 32(2), e00041-18.
Garvey, M. I., Bradley, C. W., Wilkinson, M. A., Holden, K. L., Clewer, V., &
Holden, E. (2019). The value of the infection prevention and control nurse led
MRSA ward round. Antimicrobial Resistance & Infection Control, 8(1), 53.
Harkins, C. P., Pichon, B., Doumith, M., Parkhill, J., Westh, H., Tomasz, A., ...
& Holden, M. T. (2017). Methicillin-resistant Staphylococcus aureus emerged
Staphylococcus aureus rates in surgical patients: a controlled multicentre
intervention trial. Infectious Diseases. Vol 3 (9).
Green B. N. (2012). Methicillin resistant Staphylococcus aureus: an overview
for manual therapists. J Chirop Med. Vol 11 (1), 64-75
Gigerenzer G., Wegwarth O. (2013). Five-year survival rates can mislead. BMJ.
Vol 348
Borg M. A., Camilleri L., Waisfisz B. (2012). Understanding the epidemiology
of MRSA in Europe: do we need to think outside the box? J Hosp Infect. Vol 81
(4). 251-256
Lloyd S. J. O., Svhreiber S. J., Kopp P. E et al. (2005). Superspreading and the
effect of individual variation on disease emergence. Nature. Vol 438. 355-359
Bode L. G., Kloytmans J .A., Wertherirn H. F. et al. (2010). Preventing surgical
site infections in nasal carriers of Staphylococcus aureus. N Eng J Med. 2010.
Vol 362. 9-17.
Fukunaga B. T., Sumida W. K., Taira D. A., Davis J. W., Seto T. B. (2016).
Hospital acquired methicillin resistant Staphylococcus aureus bacteremia
related to Medicare antibiotic prescriptions: a state level analysis. Hawaii J Med
Public Health. Vol 75 (10). 303-309
Littman J., Viens A. M. (2015). The ethical significance of antimicrobial
resistance. Public Health Ethics. Vol 8 (3). 209-224.
Peters C., Dulon M., Kleimuller O., Nienhaus A., Schabion A. (2017). MRSA
prevalence and risk factors among health personnel and residents in nursing
homes in Hamburg, Germany-a cross sectional study. PLoS One. Vol 12 (1).
E0169425
Galar, A., Weil, A. A., Dudzinski, D. M., Muñoz, P., & Siedner, M. J. (2019).
Methicillin-Resistant Staphylococcus aureus Prosthetic Valve Endocarditis:
Pathophysiology, Epidemiology, Clinical Presentation, Diagnosis, and
Management. Clinical microbiology reviews, 32(2), e00041-18.
Garvey, M. I., Bradley, C. W., Wilkinson, M. A., Holden, K. L., Clewer, V., &
Holden, E. (2019). The value of the infection prevention and control nurse led
MRSA ward round. Antimicrobial Resistance & Infection Control, 8(1), 53.
Harkins, C. P., Pichon, B., Doumith, M., Parkhill, J., Westh, H., Tomasz, A., ...
& Holden, M. T. (2017). Methicillin-resistant Staphylococcus aureus emerged
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long before the introduction of methicillin into clinical practice. Genome
biology, 18(1), 130.
Lee, A. S., de Lencastre, H., Garau, J., Kluytmans, J., Malhotra-Kumar, S.,
Peschel, A., & Harbarth, S. (2018). Methicillin-resistant Staphylococcus aureus.
Nature reviews Disease primers, 4, 18033.
Turner, N. A., Sharma-Kuinkel, B. K., Maskarinec, S. A., Eichenberger, E. M.,
Shah, P. P., Carugati, M., ... & Fowler, V. G. (2019). Methicillin-resistant
Staphylococcus aureus: an overview of basic and clinical research. Nature
Reviews Microbiology, 1.
Walrath, J. M., Immelt, S., Ray, E. M., van Graafeiland, B., & Himmelfarb, C.
D. (2015). Preparing patient safety advocates: Evaluation of nursing students’
reported experience with authority gradients in a hospital setting. Nurse
educator, 40(4), 174-178.
Werner, C., & Shaban, R. Z. (2018). Successfully clearing discharged patients
of methicillin-resistant Staphylococcus aureus: Opportunities for the prevention
and containment of antimicrobial resistance. Infection, disease & health, 23(1),
57-62.
Werner, C., Zimmerman, P. A., & Elder, E. (2016). Hospital based clearance of
patients with skin and soft tissue methicillin resistant Staphylococcus aureus
(MRSA): a systematic review of the literature. Infection, Disease & Health,
21(2), 72-83.
Appendix 1
biology, 18(1), 130.
Lee, A. S., de Lencastre, H., Garau, J., Kluytmans, J., Malhotra-Kumar, S.,
Peschel, A., & Harbarth, S. (2018). Methicillin-resistant Staphylococcus aureus.
Nature reviews Disease primers, 4, 18033.
Turner, N. A., Sharma-Kuinkel, B. K., Maskarinec, S. A., Eichenberger, E. M.,
Shah, P. P., Carugati, M., ... & Fowler, V. G. (2019). Methicillin-resistant
Staphylococcus aureus: an overview of basic and clinical research. Nature
Reviews Microbiology, 1.
Walrath, J. M., Immelt, S., Ray, E. M., van Graafeiland, B., & Himmelfarb, C.
D. (2015). Preparing patient safety advocates: Evaluation of nursing students’
reported experience with authority gradients in a hospital setting. Nurse
educator, 40(4), 174-178.
Werner, C., & Shaban, R. Z. (2018). Successfully clearing discharged patients
of methicillin-resistant Staphylococcus aureus: Opportunities for the prevention
and containment of antimicrobial resistance. Infection, disease & health, 23(1),
57-62.
Werner, C., Zimmerman, P. A., & Elder, E. (2016). Hospital based clearance of
patients with skin and soft tissue methicillin resistant Staphylococcus aureus
(MRSA): a systematic review of the literature. Infection, Disease & Health,
21(2), 72-83.
Appendix 1
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