Abstract

The Médecins Sans Frontières Tertiary Orthopaedic Care center in Mosul, Iraq, provides reconstructive surgery, microbiological analysis, integrated infection prevention and control, and antibiotic stewardship services. Between May 2018 and February 2020, we recorded soft tissue and/or bone infections caused by gram-negative extensively drug-resistant (XDR) bacteria in 4.9% (13/266) of the admitted patients. The XDR bacteria identified among 12 patients in this case series were extended-spectrum β-lactamase–producing Klebsiella pneumoniae (n = 5, 41.7%) with intermediate sensitivity or resistance to imipenem and/or meropenem, Acinetobacter spp (n = 3, 25.0%; 2 Acinetobacter baumannii strains) resistant to imipenem and/or meropenem, Pseudomonas aeruginosa (n = 2, 16.7%) resistant to imipenem and meropenem, and extended-spectrum β-lactamase–producing Proteus mirabilis (n = 2, 16.7%) resistant to meropenem. Most XDR isolates were sensitive only to colistin or polymyxin B, neither of which is available in Iraq. Therefore, the only treatment option was multiple rounds of surgical debridement and wound care. The infection was deemed cured before discharge in 7 patients (58.3%). Meanwhile, 4 patients (33.3%) were discharged with unhealed wounds, and outpatient follow-up was planned. One patient died in the intensive care unit of a referral hospital after developing septicemia postsurgery. XDR bacteria pose substantial health risks in Iraq. Thus, improving antimicrobial stewardship and accessibility to essential antibiotics is critical to address this issue.

Antimicrobial resistance (AMR), an increasing global health threat [1, 2], is prevalent in patients with surgical trauma wounds in conflict-affected settings such as Mosul, Iraq [3–6]. Patients with surgical trauma, particularly those in low-resource and conflict-affected areas, face severe consequences when wounds become infected by drug-resistant bacteria, as infection leads to increased mortality, prolonged hospital stay, and severe economic losses for the patient and health systems [7–9]. A high prevalence of multidrug-resistant (MDR) infections has been identified in patients with trauma-related wounds [10]. In particular, extensively drug-resistant (XDR) bacteria represent a major concern. XDR infections have fewer treatment options, and such treatments are not easily accessible in low-resource settings [11].

Evidence on XDR infections in Iraq is scarce, with no reports from Mosul regarding the population with conflict-associated wounds [12, 13]. Therefore, this case series described the characteristics, clinical management, and outcomes of patients admitted with conflict-associated wounds complicated by XDR infections to the Médecins Sans Frontières (MSF) Tertiary Orthopaedic Care (TOC) center in East Mosul, Iraq, between May 2018 and February 2020.

MATERIALS AND METHODS

Setting

Mosul, which has been heavily affected by decades of conflict (most recently in 2017), has a deteriorated public health system [14]. MSF has been performing free orthopedic and reconstructive surgery since May 2018 at the TOC in East Mosul, adopting a multidisciplinary approach including surgery, physiotherapy, mental health care, and wound care. Infection prevention and control (IPC) measures, access to microbiology diagnostics, and antibiotic stewardship programs were established in response to the significant burden of MDR.

Study Design and Population

This retrospective case series investigated the clinical and microbiological characteristics of patients admitted to MSF TOC in Mosul who were diagnosed with XDR infection between May 2018 and February 2020.

Definition of XDR

XDR was defined as nonsusceptibility to at least 1 agent in all but ≤2 antimicrobial categories per the corresponding antibiogram, as stipulated by the international expert proposal for standard definitions for acquired resistance [15]. In microorganisms with intrinsic resistance to an antibiotic or antibiotic class, the antibiotic or class was removed prior to applying the XDR definition criteria. Only antibiotic families available within the country were tested. Therefore, the susceptibility of organisms to antibiotics that are not available in Iraq was not considered in the assessment of XDR resistance. This approach ensured that the classification of XDR was applicable and relevant to the treatments available in Iraq. If an antibiotic class was not tested, no assumption was made regarding bacterial susceptibility.

Microbiological and Clinical Procedures

Antibiotic sensitivity testing was performed with the Kirby-Bauer disk diffusion method [16]. No other tests were performed. The interpretation was based on the guidelines of the Clinical and Laboratory Standards Institute [17] and performed in an external microbiology laboratory in Erbil (>80 km from Mosul). Extended-spectrum β-lactamase (ESBL) production was determined by detecting the synergy between clavulanic acid and a third-generation cephalosporin indicator. Testing was performed for all antibiotic classes available in Iraq. The guidelines do not have a breakpoint zone diameter for interpreting polymyxin B and colistin. In Iraq, testing for colistin was not available.

On admission, patients with signs of infection underwent biopsy at least 1 week after antibiotic washout following the MSF guidelines with clinical, blood, and radiologic examinations. In addition to the clinical assessment of the wound, the severity of the infection was assessed weekly by measuring C-reactive protein levels and the erythrocyte sedimentation rate. The technical procedures for debridement, wound care, and final suture after infection resolution followed the MSF guidelines [18].

Data Collection

Information on XDR isolates was retrospectively collected from the WHONET microbiology laboratory database, which is routinely used in the TOC. Sociodemographic and clinical data were extracted from our routine database and patients’ medical records.

Patient outcomes were categorized as cured (no clinical infection signs, complete wound healing with no pus discharge, and normal C-reactive protein and erythrocyte sedimentation rate levels), uncured (outpatient follow-up required), or deceased at discharge.

RESULTS

Between May 2018 and February 2020, 266 patients with a microbiologically confirmed infection were admitted to the MSF TOC in Mosul. More than half of these infections were caused by gram-positive bacteria (135/266, 50.8%), whereas the remainder were caused by gram-negative bacteria (131/266, 49.2%). Among the gram-negative bacteria, 67.9% (89/131) were ESBL producers. In total, 126 of 131 gram-negative bacteria were tested for carbapenem resistance with imipenem or meropenem, revealing that 23.8% of the isolates (30/126) were carbapenem resistant. Of the total patient cohort, 4.9% (13/266) were infected by an XDR organism, comprising 9.9% (13/131) of all gram-negative infections, and all of these organisms were gram negative. Twelve patients were included in this case series, and their characteristics are presented in Table 1. One patient was excluded because of incomplete records.

Table 1.

Demographics and Clinical Characteristics of Patients With Extensively Drug-Resistant Infections Admitted May 2018–February 2020 in Mosul, Iraq

No.SexAge, yOPD Admission, No.Nature of InjurySite of InjuryInfection TypeAntibiotics Provided (All IV)Treatment Duration, dComorbiditiesRadiologyLOS, dDebridement, No.Outcome
1M2410Road traffic injuryLower limbPolymicrobialVancomycin, 1 g; imipenem, 1 g; gentamycin, 280 mg; colistin, 9 000 000-IU loading dose switched to 4 500 0008NoneOsteomyelitis3014Cured
2M30NABedsoreBackPolymicrobialLevofloxacin, 500 mg; amikacin, 750 mg13NoneNo bone involvement453Uncured
3M32NABedsoreBackPolymicrobialAmikacin, 1 g; ceftriaxone, 2 g78Neurologic disorderaNo bone involvement1203Died
4F69NADiabetic footFootPolymicrobialGentamycin, 160 mg; cefazolin, 1 g; metronidazole, 500 mg; ceftriaxone, 2 gbDiabetesOsteomyelitis448Cured
5M14NABedsoreLumbar areaMonomicrobialNoneNoneNo bone involvement724Uncured
6F341Suicidal attemptForearmPolymicrobialNoneNoneNo fracture or osteomyelitis184Cured
7F522Blast injuryIliac regionPolymicrobialNoneDiabetes and hypertensionOsteomyelitis222Cured
8M17NAShell injurySacrococcygealPolymicrobialImipenem, 500 mg;
vancomycin, 1 g; amikacin, 1 g
8Neurologic disorderaNo bone involvement202Uncured
9M298Electrical burnHandPolymicrobialNoneNoneFoot amputation; no bone involvement455Cured
10M820Road traffic injuryFootMonomicrobialNoneNoneNo fracture or bone involvement227Cured
11M4219Diabetic footThighMonomicrobialNoneDiabetes and hypertensionNo bone involvement1899Cured
12M137BedsoreLumber backPolymicrobialNoneNeurologic disorderaOsteomyelitis93Uncured
No.SexAge, yOPD Admission, No.Nature of InjurySite of InjuryInfection TypeAntibiotics Provided (All IV)Treatment Duration, dComorbiditiesRadiologyLOS, dDebridement, No.Outcome
1M2410Road traffic injuryLower limbPolymicrobialVancomycin, 1 g; imipenem, 1 g; gentamycin, 280 mg; colistin, 9 000 000-IU loading dose switched to 4 500 0008NoneOsteomyelitis3014Cured
2M30NABedsoreBackPolymicrobialLevofloxacin, 500 mg; amikacin, 750 mg13NoneNo bone involvement453Uncured
3M32NABedsoreBackPolymicrobialAmikacin, 1 g; ceftriaxone, 2 g78Neurologic disorderaNo bone involvement1203Died
4F69NADiabetic footFootPolymicrobialGentamycin, 160 mg; cefazolin, 1 g; metronidazole, 500 mg; ceftriaxone, 2 gbDiabetesOsteomyelitis448Cured
5M14NABedsoreLumbar areaMonomicrobialNoneNoneNo bone involvement724Uncured
6F341Suicidal attemptForearmPolymicrobialNoneNoneNo fracture or osteomyelitis184Cured
7F522Blast injuryIliac regionPolymicrobialNoneDiabetes and hypertensionOsteomyelitis222Cured
8M17NAShell injurySacrococcygealPolymicrobialImipenem, 500 mg;
vancomycin, 1 g; amikacin, 1 g
8Neurologic disorderaNo bone involvement202Uncured
9M298Electrical burnHandPolymicrobialNoneNoneFoot amputation; no bone involvement455Cured
10M820Road traffic injuryFootMonomicrobialNoneNoneNo fracture or bone involvement227Cured
11M4219Diabetic footThighMonomicrobialNoneDiabetes and hypertensionNo bone involvement1899Cured
12M137BedsoreLumber backPolymicrobialNoneNeurologic disorderaOsteomyelitis93Uncured

Abbreviations: d, days; F, female; IV, intravenous; LOS, length of stay; M, male; NA, not applicable; OPD, outpatient department; y, years.

aParaplegia or spinal cord injury.

bDuration of antibiotic treatment missing for patient 4.

Table 1.

Demographics and Clinical Characteristics of Patients With Extensively Drug-Resistant Infections Admitted May 2018–February 2020 in Mosul, Iraq

No.SexAge, yOPD Admission, No.Nature of InjurySite of InjuryInfection TypeAntibiotics Provided (All IV)Treatment Duration, dComorbiditiesRadiologyLOS, dDebridement, No.Outcome
1M2410Road traffic injuryLower limbPolymicrobialVancomycin, 1 g; imipenem, 1 g; gentamycin, 280 mg; colistin, 9 000 000-IU loading dose switched to 4 500 0008NoneOsteomyelitis3014Cured
2M30NABedsoreBackPolymicrobialLevofloxacin, 500 mg; amikacin, 750 mg13NoneNo bone involvement453Uncured
3M32NABedsoreBackPolymicrobialAmikacin, 1 g; ceftriaxone, 2 g78Neurologic disorderaNo bone involvement1203Died
4F69NADiabetic footFootPolymicrobialGentamycin, 160 mg; cefazolin, 1 g; metronidazole, 500 mg; ceftriaxone, 2 gbDiabetesOsteomyelitis448Cured
5M14NABedsoreLumbar areaMonomicrobialNoneNoneNo bone involvement724Uncured
6F341Suicidal attemptForearmPolymicrobialNoneNoneNo fracture or osteomyelitis184Cured
7F522Blast injuryIliac regionPolymicrobialNoneDiabetes and hypertensionOsteomyelitis222Cured
8M17NAShell injurySacrococcygealPolymicrobialImipenem, 500 mg;
vancomycin, 1 g; amikacin, 1 g
8Neurologic disorderaNo bone involvement202Uncured
9M298Electrical burnHandPolymicrobialNoneNoneFoot amputation; no bone involvement455Cured
10M820Road traffic injuryFootMonomicrobialNoneNoneNo fracture or bone involvement227Cured
11M4219Diabetic footThighMonomicrobialNoneDiabetes and hypertensionNo bone involvement1899Cured
12M137BedsoreLumber backPolymicrobialNoneNeurologic disorderaOsteomyelitis93Uncured
No.SexAge, yOPD Admission, No.Nature of InjurySite of InjuryInfection TypeAntibiotics Provided (All IV)Treatment Duration, dComorbiditiesRadiologyLOS, dDebridement, No.Outcome
1M2410Road traffic injuryLower limbPolymicrobialVancomycin, 1 g; imipenem, 1 g; gentamycin, 280 mg; colistin, 9 000 000-IU loading dose switched to 4 500 0008NoneOsteomyelitis3014Cured
2M30NABedsoreBackPolymicrobialLevofloxacin, 500 mg; amikacin, 750 mg13NoneNo bone involvement453Uncured
3M32NABedsoreBackPolymicrobialAmikacin, 1 g; ceftriaxone, 2 g78Neurologic disorderaNo bone involvement1203Died
4F69NADiabetic footFootPolymicrobialGentamycin, 160 mg; cefazolin, 1 g; metronidazole, 500 mg; ceftriaxone, 2 gbDiabetesOsteomyelitis448Cured
5M14NABedsoreLumbar areaMonomicrobialNoneNoneNo bone involvement724Uncured
6F341Suicidal attemptForearmPolymicrobialNoneNoneNo fracture or osteomyelitis184Cured
7F522Blast injuryIliac regionPolymicrobialNoneDiabetes and hypertensionOsteomyelitis222Cured
8M17NAShell injurySacrococcygealPolymicrobialImipenem, 500 mg;
vancomycin, 1 g; amikacin, 1 g
8Neurologic disorderaNo bone involvement202Uncured
9M298Electrical burnHandPolymicrobialNoneNoneFoot amputation; no bone involvement455Cured
10M820Road traffic injuryFootMonomicrobialNoneNoneNo fracture or bone involvement227Cured
11M4219Diabetic footThighMonomicrobialNoneDiabetes and hypertensionNo bone involvement1899Cured
12M137BedsoreLumber backPolymicrobialNoneNeurologic disorderaOsteomyelitis93Uncured

Abbreviations: d, days; F, female; IV, intravenous; LOS, length of stay; M, male; NA, not applicable; OPD, outpatient department; y, years.

aParaplegia or spinal cord injury.

bDuration of antibiotic treatment missing for patient 4.

The median age of patients in the case series was 29.5 years (IQR, 15.5–38). They were predominantly male (n = 9, 75.0%). Six patients (50.0%) reported comorbidities. The median hospital stay was 37 days (IQR, 21–58.5), and patients underwent a median of 4 operations (IQR, 3–7.5) during their stay. All patients presented with clinical signs of infection on admission. Most injuries (n = 9, 75.0%) resulted from nonviolent trauma, whereas 3 (25.0%) resulted from violent trauma, namely blast injuries. The limbs were the most prevalent site of injury (n = 7, 58.3%). Most patients had soft tissue infections (n = 7, 58.3%), and 5 (41.7%) also had bone involvement (Table 1).

Of the episodes, 9 (75.0%) were polymicrobial and 3 (25.0%) were monomicrobial. At least 1 XDR isolate was identified in each episode. In addition to other transmission-based precautions, all patients were placed in single-bed isolation rooms.

The most prevalent XDR organism was ESBL-producing Klebsiella pneumoniae (n = 5, 41.7%), exhibiting resistance or intermediate sensitivity to imipenem and/or meropenem. Other XDR isolates included Acinetobacter spp (n = 3, 25.0%), with resistance to imipenem and/or meropenem; Pseudomonas aeruginosa (n = 2, 16.7%), showing resistance to imipenem and meropenem; and ESBL-producing Proteus mirabilis (n = 2, 16.7%), with meropenem resistance (Figure 1). All isolated XDR organisms were gram negative. In polymicrobial episodes, additional pathogens included methicillin-resistant Staphylococcus aureus, Enterococcus spp, Escherichia coli, viridans streptococci, and Burkholderia cepacia.

Type and proportion of bacteria isolated in bone biopsies from patients with extensively drug-resistant infections in Mosul, Iraq, May 2018−February 2020.
Figure 1.

Type and proportion of bacteria isolated in bone biopsies from patients with extensively drug-resistant infections in Mosul, Iraq, May 2018−February 2020.

Antibiotic susceptibility testing identified colistin and polymyxin B as the only potential treatments for XDR infections; however, neither drug is available in the country. Tigecycline resistance was noted in 71.4% (5/7) of tested isolates. Newer antibiotics, such as ceftazidime-avibactam or meropenem-vaborbactam, are not on MSF's essential medications list because of economic barriers and a lack of local efficacy data, resulting in reliance on surgical management, primarily debridement and subsequent wound care.

Seven patients (58.3%) were treated solely by surgical debridement. All patients who received antibiotics had polymicrobial infections. Antibiotics included ceftriaxone, amikacin, levofloxacin, gentamycin, and imipenem, and they were provided as slow infusions coupled with renal and liver monitoring to prevent side effects. One case required amputation of the lower limb.

The wounds of 7 patients (58.3%) were healed before discharge, and 4 patients (33.3%) were discharged with unhealed wounds and ongoing outpatient follow-up. One patient transferred to intensive care died from postoperative septicemia.

DISCUSSION

Our study highlights the challenges of XDR infections in Mosul, Iraq, where specific antibiotic treatment options remain scarce [19], contributing to the global burden of AMR [20].

Data paucity on XDR infections in conflict-affected areas such as the Middle East [10, 21]—worsened by conflict-driven AMR contributors, such as collapsed health systems, limited staff training, restricted availability and misuse of antibiotics, inadequate IPC measures, and poor diagnostic capacity—exacerbates AMR issues [21–23]. This series highlighted the imminent threat of XDR gram-negative bacteria, recognized as critical pathogens of global health priority according to the World Health Organization, in Mosul, Iraq [24].

Of particular concern is the impact of XDR infections on the young study population, potentially resulting in prolonged disability during their peak productive years, thereby emphasizing the urgent need for (1) strengthened AMR surveillance in Iraq to address the emergence of XDR infections and contain transmission, (2) context-adapted IPC measures, and (3) improved diagnostic capabilities for better antimicrobial stewardship.

In Mosul, colistin and polymyxin B were often the only treatment options for some XDR infections. Regarding non–Pseudomonas aeruginosa infections, tigecycline, which is often not available for testing in external laboratories, was an option; however, it was not accessible because of supply shortages. The scarcity of these drugs alongside tigecycline resistance severely restricted therapeutic options. Therefore, access to essential antibiotics such as colistin and tigecycline [11, 25], which are recognized as last-resort antibiotics against MDR pathogens [26], is critical for the treatment of XDR infections caused by gram-negative bacteria in Iraq [27]. Novel antibacterial agents such as β-lactam/β-lactamase inhibitor combinations, representing promising alternatives against MDR and XDR infections [28], have not yet been added to MSF's essential medication list because the local resistance patterns, which are critical for selecting relevant antibiotics, have not been clarified. The high costs associated with these new antibiotics, which are up to 20-fold more expensive than older alternatives for carbapenem-resistant Enterobacterales, MDR Pseudomona aeruginosa, and carbepenem-resistant Acinetobacter baumannii [29], represent a significant barrier to accessibility. Despite potential availability through MSF support, ensuring a continuous and sustainable supply of these expensive drugs in low-resource settings remains challenging. Considering the growing issue of AMR worldwide, there is a pressing need to ensure access to established and emerging antibiotics in low-resource settings to effectively manage infections and save lives.

Although we advocate for improved antibiotic access, we emphasize the need for alternative strategies such as surgical debridement and subsequent wound care for managing AMR infections in extreme situations in which necessary antibiotics are unavailable. Although this approach provides effective wound healing, as presented in this study, aiming at definitive source control might be insufficient to treat complex infections such as osteomyelitis [30], in which concurrent targeted antibiotic therapy is often necessary to prevent early relapse and complications. This study did not monitor whether cured patients who were released without further antibiotic therapy later experienced relapse.

Beyond antibiotic treatment and surgery, quality IPC measures such as placing patients in single-room isolation are essential in this context to prevent XDR transmission within the facilities. The identification of XDR cases in an MSF facility highlights the broader public health concern of XDR pathogen circulation in the community and other facilities in Mosul, particularly when surgical care is the only option amid limited antibiotic accessibility.

CONCLUSION

XDR infection poses a substantial challenge in Mosul, Iraq. XDR infection management in this setting highlights the critical role of surgical management in a context in which access to essential antibiotics is problematic. Although larger studies are needed to clarify the actual prevalence of XDR infection in Mosul, improved accessibility to older and newer antibiotics is necessary to ensure appropriate XDR infection management and prevent further transmission.

Notes

Acknowledgments. We thank the MSF TOC staff for their continuous work toward improving patients’ outcomes, as well as our patients who trusted us throughout their clinical management. This series report was produced as part of the activities of the TOC center of MSF in Mosul, Iraq, which is maintained with MSF funding.

Author contributions. E. A. and K. M. conceptualized the idea. All authors contributed to the write-up of the study protocol, including design and methodology. H. A. A., H. H. M., H. H. A. S., and A. N. T. supported the collection of the data. H. A. A. and K. M. were responsible of data curation. Analysis of the results was done by H. A. A. with the support and validation of A. W. and K. M. All authors discussed and supported the interpretation of the results. H. A. A. drafted the original manuscript with the support of P. G.-V. and K. M. K. M. supervised the project. All authors reviewed the results and approved the last version of the manuscript.

Data availability. Data presented in this study are not available publicly but upon request to interested researchers due to confidentiality and contextual privacy concerns.

Patient consent statement. This research was approved by the MSF Ethics Review Board under protocol 2086 (16/12/2020) and by the Ministry of Health and Environment of the Nineveh Health Directorate in Iraq under protocol number 31210 (08/12/2020). All patient data used in this study were pseudoanonymized and did not include direct patient identifiers. Written consent from patients was waived by the MSF and local ethics committees following the nature of the study design.

Financial support. This study did not receive any funding. The work was supported by Médecins Sans Frontières.

References

1

World Health Organization
. Antimicrobial resistance. Available at: https://www.who.int/news-room/fact-sheets/detail/antimicrobial-resistance. Accessed 8 January 2024.

2

EClinicalMedicine
.
Antimicrobial resistance: a top ten global public health threat
.
EClinicalmedicine
 
2021
;
41
:
101221
.

3

Abbara
 
A
,
Rawson
 
TM
,
Karah
 
N
, et al.  
Antimicrobial resistance in the context of the Syrian conflict: drivers before and after the onset of conflict and key recommendations
.
Int J Infect Dis
 
2018
;
73
:
1
6
.

4

Moussally
 
K
,
Abu-Sittah
 
G
,
Gomez
 
FG
,
Fayad
 
AA
,
Farra
 
A
.
Antimicrobial resistance in the ongoing Gaza war: a silent threat
.
Lancet
 
2023
;
402
:
1972
3
.

5

Haraoui
 
L-P
,
Valiquette
 
L
,
Laupland
 
KB
.
Antimicrobial resistance in conflicts
.
J Assoc Med Microbiol Infect Dis Can
 
2018
;
3
:
119
22
.

6

Petrosillo
 
N
,
Petersen
 
E
,
Antoniak
 
S
.
Ukraine war and antimicrobial resistance
.
Lancet Infect Dis
 
2023
;
23
:
653
4
.

7

Birgand
 
G
,
Dhar
 
P
,
Holmes
 
A
.
The threat of antimicrobial resistance in surgical care: the surgeon's role and ownership of antimicrobial stewardship
.
Br J Surg
 
2023
;
110
:
1567
9
.

8

Sharma
 
A
,
Singh
 
A
,
Dar
 
MA
, et al.  
Menace of antimicrobial resistance in LMICs: current surveillance practices and control measures to tackle hostility
.
J Infect Public Health
 
2022
;
15
:
172
81
.

9

Poudel
 
AN
,
Zhu
 
S
,
Cooper
 
N
, et al.  
The economic burden of antibiotic resistance: a systematic review and meta-analysis
.
PLoS One
 
2023
;
18
:
e0285170
.

10

M’Aiber
 
S
,
Maamari
 
K
,
Williams
 
A
, et al.  
The challenge of antibiotic resistance in post-war Mosul, Iraq: an analysis of 20 months of microbiological samples from a tertiary orthopaedic care centre
.
J Glob Antimicrob Resist
 
2022
;
30
:
311
8
.

11

World Health Organization
.
The WHO AWaRe (access, watch, reserve) antibiotic book
.
2022
. Available at: https://dgpi.de/wp-content/uploads/2022/12/AWaRe-Antibiotic-Book_WHO_Dez2022.pdf

12

Aryan
 
G
.
Antimicrobial susceptibility of extensively drug-resistant (XDR) and multidrug-resistant (MDR) Pseudomonas aeruginosa isolated from patients in Erbil city
.
2017
. Available at: https://hmu.edu.krd/images/Medicine/Conference/2-5.pdf

13

Al-Hasnawy
 
HH
,
Judi
 
MR
,
Hamza
 
HJ
.
The dissemination of multidrug resistance (MDR) and extensively drug resistant (XDR) among uropathogenic E coli (UPEC) isolates from urinary tract infection patients in Babylon Province, Iraq
.
Baghdad Science Journal
 
2019
;
16
:
0986
.

14

Muntather
 
H.
 
Right to health in Iraq—Fragile structures and growing challenges
.
2023
. Available at: https://annd.org/uploads/publications/Right_to_health_in_Iraq_Fragile_structures_and_growing_challenges_Muntather_Hassan_En.pdf

15

Magiorakos
 
AP
,
Srinivasan
 
A
,
Carey
 
RB
, et al.  
Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance
.
Clin Microbiol Infect
 
2012
;
18
:
268
81
.

16

Drew
 
WL
,
Barry
 
AL
,
O’Toole
 
R
,
Sherris
 
JC
.
Reliability of the Kirby-Bauer disc diffusion method for detecting methicillin-resistant strains of Staphylococcus aureus
.
Appl Microbiol
 
1972
;
24
:
240
7
.

17

Clinical and Laboratory Standards Institute
.
Performance standards for antimicrobial susceptibility testing—29th edition
.
2019
. Available at: https://clsi.org/media/2663/m100ed29_sample.pdf

18

Medecins Sans Frontieres.
 
Treatment of a simple wound: MSF medical guidelines
. Available at: https://medicalguidelines.msf.org/en/viewport/CG/english/treatment-of-a-simple-wound-18482379.html. Accessed 5 February 2024.

19

Bassetti
 
M
,
Garau
 
J
.
Current and future perspectives in the treatment of multidrug-resistant gram-negative infections
.
J Antimicrob Chemother
 
2021
;
76
:
iv23
37
.

20

Murray
 
CJ
,
Ikuta
 
KS
,
Sharara
 
F
, et al.  
Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis
.
Lancet
 
2022
;
399
:
629
55
.

21

Abou Fayad
 
A
,
Rizk
 
A
,
El Sayed
 
S
, et al.  
Antimicrobial resistance and the Iraq wars: armed conflict as an underinvestigated pathway with growing significance
.
BMJ Global Health
 
2023
;
7
(
suppl 8
):
e010863
.

22

Devi
 
S
.
AMR in the Middle East: “a perfect storm.”
 
Lancet
 
2019
;
394
:
1311
2
.

23

Pallett
 
SJC
,
Boyd
 
SE
,
O'Shea
 
MK
et al.  et al.  
The contribution of human conflict to the development of antimicrobial resistance
.
Commun Med
 
2023
;
3
:
153
.

24

World Health Organization
.
Prioritization of pathogens to guide discovery, research and development of new antibiotics for drug-resistant bacterial infections, including tuberculosis
. Available at: https://www.who.int/publications-detail-redirect/WHO-EMP-IAU-2017.12. Accessed 10 January 2024.

25

World Health Organization
.
2023
.
World Health Organization model list of essential medicines—23rd list
. Available at: https://iris.who.int/bitstream/handle/10665/371090/WHO-MHP-HPS-EML-2023.02-eng.pdf? sequence=1

26

Osei Sekyere
 
J
,
Govinden
 
U
,
Bester
 
LA
,
Essack
 
SY
.
Colistin and tigecycline resistance in carbapenemase-producing gram-negative bacteria: emerging resistance mechanisms and detection methods
.
J Appl Microbiol
 
2016
;
121
:
601
17
.

27

LaPlante
 
K
,
Cusumano
 
J
,
Tillotson
 
G
.
Colistin for the treatment of multidrug-resistant infections
.
Lancet Infect Dis
 
2018
;
18
:
1174
5
.

28

Karaiskos
 
I
,
Lagou
 
S
,
Pontikis
 
K
,
Rapti
 
V
,
Poulakou
 
G
.
The “old” and the “new” antibiotics for MDR Gram-negative pathogens: for whom, when, and how
.
Front Public Health
 
2019
;
7
:
151
.

29

Yahav
 
D
,
Shepshelovich
 
D
,
Tau
 
N
.
Cost analysis of new antibiotics to treat multidrug-resistant bacterial infections: mind the gap
.
Infect Dis Ther
 
2021
;
10
:
621
30
.

30

Momodu
 
II
,
Savaliya
 
V.
 
Osteomyelitis
.
Treasure Island, FL
:
StatPearls Publishing
.
2024
. Available at: http://www.ncbi.nlm.nih.gov/books/NBK532250/. Accessed 6 February 2024.

Author notes

Potential conflicts of interest. All authors: No reported conflicts.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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