CURRENT TREND OF RESISTANT FOR THE COMMONLY PRESCRIBED NEW FLUOROQUINOLONES AMONG HOSPITALISED PATIENTS IN SANA'A, YEMEN
Ali Alyahawi1*, Ali Alkaf2, Taha Alnosary3
1Department of Pharmacy, Al-Razi University, Yemen
2Faculty of Pharmacy, Sana'a University, Yemen
3Department of Microbiology, the National University, Yemen
DOI: https://doi.org/10.22270/ujpr.v3i5.197
The new fluoroquinolones have demonstrated enhanced activity against the most common bacteria involved in lower respiratory tract infection (LRTI). Moxifloxacin is the most commonly prescribed respiratory flouroquinolone drug in Yemen. Pneumonia is a major and an on-going public health problem globally. With the widely use of fluoroquinolones in the clinical practice, the potential for developing resistance has become a concern. The aim of present study was to determine the trend of moxifloxacin resistant and the distribution of resistant for different sample types among hospitalised patients in Sana'a, Yemen. The study was performed at a private hospital in Sana’a, Yemen. The records were taken from the microbiology department for hospitalised patients. Moxifloxacin susceptibility samples were collected from January, 2017 to December, 2017. The moxifloxacin susceptibility was studied against several isolates. Full ethical clearance was obtained from the qualified authorities who approved the study design. All data were analyzed using SPSS Statistics version 21. Out of 927 sample isolates, 580 (62.6%) were moxifloxacin resistant isolates and only 30.1% were sensitive. The Escherichia coli was observed in 24.4% of total sample isolates, followed by Pseudomonas aeruginosa (12.1%). From the study findings, 44.8% of total sample was isolated from sputum cultures. There was a statistically significant difference between bacteria type and culture results (P-value < 0.001). Moreover, 96.2% of Acinetobacter species and all Acinetobacter baumannii isolates were moxifloxacin resistant. The study findings reported that 70.4% of Escherichia coli isolates were resistant for moxifloaxin, followed by methicillin resistant staphylococcus aureus (64.7%), Klebsiella pneumonia (60.6%), and Pseudomonas aeruginosa (46.4%). However, 86.1% of staphylococcus aureus isolates were moxifloxacin sensitive. Results in this study showed that there was high significantly relationship between culture results and sample type (P-value< 0.001). Also 44.8% of sample isolates were from sputum cultures. Moreover, 74.2% of sputum cultures isolates were moxifloxacin resistant. There was a statistically significant difference between culture results with age groups (P-value = 0.02). Also 64.1% of males had moxifloxacin resistant and 36.9% of isolate resistant were aged > 60 years. This study reveals that varieties of pathogens are responsible for LRTI and moxifloxacin resistance has become a great public health issue. The possibility of reducing resistance by controlling the use of antibiotics is a reasonable approach. Inappropriate and irrational drug usage should be avoided. This study may help the government’s regulatory authority to develop a policy about rational prescription of antibiotics to minimize resistance of new antibiotics and also to ensure the maximum safety to the health of patients.
Keywords: Moxifloxacin, prevalence, resistance.
INTRODUCTION
The classic fluoroquinolones such as ciprofloxacin, norfloxacin, fleroxacin and ofloxacin have had strong activity against Gram-negative bacteria, but the effectiveness of these compounds against Gram-positive bacteria has been debated. The new fluoroquinolones developed during the 1990s, such as levofloxacin and moxifloxacin, have demonstrated enhanced activity against the most common bacteria involved in lower respiratory tract infection (LRTI).The mechanism of newer fluoroquinolone activity is the inhibition of essential bacterial type II topoisomerases (DNA gyrase) and topoisomerase IV1. All new fluoroquinolones have a bactericidal activity and a post-antibiotic effect. Compared with ciprofloxacin, all new fluoroquinolones have a longer elimination half-life that allows once daily dosing. In addition, these antibiotics have excellent penetration into respiratory tissues, with the highest concentrations found in the epithelial lining fluid and alveolar macrophages2. The newer fluoroquinolones such as levofloxacin and moxifloxacin are currently available in both IV and oral formulations. With regard to the pharmacodynamic characteristics, the new fluoroquinolones cause concentration-dependent killing3.
Moxifloxacin (Avelox; Bayer), a “fourth-generation” fluoroquinolone, is often used in the empirical treatment of severe community-acquired pneumonia (CAP), which is one of the most common infectious diseases and among the primary causes of death worldwide4. Streptococcus pneumoniae is the primary pathogen responsible for CAP, but many other microorganisms, including Gram-negative and atypical bacteria (e.g., Legionella pneumophila, Mycoplasma pneumoniae, and Chlamydophila pneumoniae), may also be etiological agents5. The recommended dose of moxifloxacin is 400 mg/day (q.d.). No dosage adjustment is required in elderly patients, obese patients6, or patients with renal or mild hepatic impairment7. Furthermore, due to the risk of a prolonged QT interval (a measure of the time between the start of the Q wave and the end of the T wave inthe heart’s electrical cycle), it is recommended that the daily dose of moxifloxacin should not exceed 400 mg8. The clinical efficacy of the newer fluoroquinolones in the treatment of LRTI has been demonstrated in several randomized, double-blind, prospective studies. In comparative community-acquired pneumonia (CAP) studies, newer fluoroquinolones almost have more activity than the cephalosporins (e.g. ceftriaxone, cefaclor or cefuroxime axetil) and the macrolides (e.g. erythromycin or roxithromycin)1. Niederman et al.9 compared hospitalization and mortality in patients with CAP being treated with moxifloxacin, amoxicillin or clarithromycin. The mortality rate for moxifloxacin-treated patients was significantly better (P= 0.045) than for comparator-treated patients. Current treatment guidelines for the management of LRTI in adults recommend fluoroquinolones for empirical treatment in several patient groups. The new fluoroquinolones currently available offer major therapeutic advances compared with previous agents, and the incidence of adverse events is clearly outweighed by their clinically use1. As with other antimicrobial, the development of resistance is a potential problem associated with their increased use in RTIs. Rational prescribing and continous control of antibiotic resistance levels are needed to keep their future antibacterial efficacy. Moxifloxacin is a new broad-spectrum antibacterial agent against the most common bacteria involved in LRTI. Moxifloxacin is the commonly prescribed respiratory flouroquinolone drug in Yemen. Pneumonia is a major and an on-going public health problem globally. Thus, the aim of present study was to determine the trends of moxifloxacin and the distribution of resistant for different sample types among hospitalised patients in Sana'a, Yemen.
METHODS
This retrospective study was performed at a private hospital in Sana’a, Yemen. Moxifloxacin susceptibility samples were collected from January, 2017 to December, 2017 from the records of hospitalised patients. The moxifloxacin susceptibility was studied against several isolates. Full ethical clearance was obtained from the qualified authorities who approved the study design. All data were analyzed using SPSS Statistics version 21.
RESULTS
According to the present study, the mean age of study sample (n=927) was 49 years (with SD ± 21.3 year) and ranged between 1 and 120 years. Out of 927 samples, 580 (62.6%) were moxifloxacin resistant isolates and only 30.1% were sensitive. Also (69.0%) of total patients were females and (31.0%) were males. Among 927 of patients, (28.2%) was aged between 41- 60 years and 35.5% more than 60 years. The Escherichia coli was observed in 24.4% of total sample isolates, followed by Pseudomonas aeruginosa (12.1%). From the study findings, 44.8% of total sample was isolated from sputum cultures (Table 1).
Results in Table 3 indicated that the relationship between bacteria type and culture results was statistically significant (P-value < 0.001). In the present study, 96.2% of Acinetobacter species were moxifloxacin resistant and all Acinetobacter baumannii isolates were moxifloxacin resistant. Also the study findings reported that 70.4% of Escherichia coliisolates were resistant for moxifloaxin, followed by Klebsiella pneumonia (60.6%), methicillin resistant staphylococcus aureus (64.7%), pseudomonas aeruginosa (46.4%). However, 86.1% of staphylococcus aureus isolates were moxifloxacin resistant. There was not statistically significant difference between culture results with sex (P-value=0.25). However, there was a statistically significant difference between culture results with age groups (P-value= 0.02). Also 64.1% of male shadmoxifloxacin resistant and 36.9% of isolate resistant were aged >60 years (Table 3). The relationship between culture results and sample type was analyzed in the Table 4. Results in this table showed that there was high significantly relationship (P-value<0.001). Also 44.8% of sample isolates were from sputum cultures. Moreover, 74.2% of sputum cultures isolates were moxifloxacin resistant.
DISCUSSION
The primary objective in the development of moxifloxacin was to produce an appropriate spectrum antibiotic for the treatment of community-acquired RTIs with a good tolerability profile, good efficacy against the relevant pathogens, and low propensity for the development of bacterial resistance, thus benefiting patients and helping clinicians to treat these diseases10. An effective new antimicrobial agent is necessary in light of the therapeutic problems posed by the increasing prevalence of antibiotic resistance of the common respiratory tract pathogens, which have become increasingly resistant to traditional first-line antibiotics such as penicillins and macrolides11. According to the study results, 62.6% of study sample were moxifloxacin resistant isolates and only 30.1% were sensitive. Moxifloxacin treatment failure is being increasingly reported, particularly in the Asia-Pacific region along with increasing detection rates of resistance mutations12.
Fluoroquinolone resistance is rare in North America. Surveillance studies in the United States from 1987 to2009 demonstrated low rates of resistance to moxifloxacin (0.1%)13. Similarly, the prevalence of fluoroquinolone resistance in Canada remained low from 1998 to 2009. Although total per capita outpatient use of fluoroquinolones increased during this 10-year period, levofloxacin and moxifloxacin resistance remained unchanged at <2% in the >26,000 isolates collected14. In contrast to study findings in Pakistan, the prevalence of Moxifloxacin resistant was 42.4%15. From the present study findings, 44.8% of total sample was isolated from sputum cultures. Moreover, 74.2% of sputum cultures isolates were moxifloxacin resistant. The increasing resistance to antibiotics by respiratory pathogens has complicated the use of empirical treatment with traditional agents and a definitive bacteriological diagnosis and susceptibility testing would be required for effective management of LRTI16. The study findings reported that 70.4% of Escherichia coli isolates were resistant for moxifloaxin, followed MRSA (64.7%), Klebsiella pneumonia (60.6%), and Pseudomonas aeruginosa (46.4%). Also results in this study showed that t there was a statistically significant difference between culture results with age groups and 36.9% of patients with moxifloxacin resistant isolates were aged>60 years.
During the last several years, resistance to fluoroquinolones has remained very high among MRSA, P. aeruginosa and in pathogens isolated from patients inside intensive care unit-patients. In addition, the recent reports ofan overall increase in resistance to fluoroquinolones among bacteria causing community-acquired infections, such as E. coli have a major concern in clinical practice. These surveillance data demonstrate that fluoroquinolone resistance has to be associated with both particular bacterial species and patient populations13.
CONCLUSION AND RECOMMENDATION
LRTIs comprise a wide range of diseases from acute bronchitis to severe pneumonia leading to death. This study reveals that varieties of pathogens are responsible for LRTI and moxifloxacin resistance has become a great public health issue. The possibility of reducing resistance by controlling the use of antibioticsis a reasonable approach. Inappropriate and irrational drug usage should be avoided. This study may help the Government’s regulatory authority to develop a policy about rational prescription of antibiotics to minimize resistance of new antibiotics and also to ensure the maximum safety to the health of patients.
CONFLICT OF INTEREST
The authors declare that no conflict of interest is associated with this work.
REFERENCES
Figure 1: Distribution of Moxifloxacin Susceptibility among Study Sample
Table 1: Distribution of Study variables
Variable |
Level of variable |
Frequency |
Percent |
Culture Result |
I |
68 |
7.3 |
R |
580 |
62.6 |
|
S |
279 |
30.1 |
|
Total |
927 |
100.0 |
|
Sex
|
M |
287 |
31.0 |
F |
640 |
69.0 |
|
Total |
927 |
100.0 |
|
Age order |
1-20 years |
124 |
13.4 |
21-40 years |
213 |
23.0 |
|
41-60 years |
261 |
28.2 |
|
60 |
329 |
35.5 |
|
Total |
927 |
100.0 |
|
Type of bacteria |
Acinetobacter baumannii |
24 |
2.6 |
Acinetobacter species |
185 |
20.0 |
|
Alpha Hemolytic Streptococcus |
2 |
0.2 |
|
B-Hemolytic Streptococcus-Group-A |
1 |
0.1 |
|
B-Hemolytic Streptococcus-Group-D |
1 |
0.1 |
|
Citrobacter Spp |
5 |
0.5 |
|
Coagulase negative Staphylococci |
57 |
6.1 |
|
Enterobacter Spp |
3 |
0.3 |
|
Enterococcus Spp |
19 |
2.0 |
|
Escherichia coli |
226 |
24.4 |
|
Klebsiella pneumoniae |
99 |
10.7 |
|
Klebsiella Spp |
50 |
5.4 |
|
Moraxella Spp |
4 |
.4 |
|
Methicillin Resistant Staphylococcus aureus(MRSA) |
17 |
1.8 |
|
Neisseria Spp |
1 |
0.1 |
|
Nocardia SPP |
1 |
0.1 |
|
Proteus mirabilis |
3 |
0.3 |
|
Proteus Spp |
10 |
1.1 |
|
Proteus vulgaris |
1 |
0.1 |
|
Pseudomonas aeruginosa |
112 |
12.1 |
|
SerratiaSpp |
4 |
0.4 |
|
Staphylococcus aureus |
72 |
7.8 |
|
Streptococcus pneumoniae |
3 |
.3 |
|
Streptococcus spp. |
27 |
2.9 |
|
Total |
927 |
100.0 |
Type of sample |
Aspirated fluid culture |
1 |
0.1 |
Blood culture |
22 |
2.4 |
|
Cerepro Spinal Fluid ( CSF ) C/S |
144 |
15.5 |
|
General swab for culture |
17 |
1.8 |
|
Pleural fluid for culture and Sensitivity |
27 |
2.9 |
|
Ascitic fluid c/s and sensitivity |
6 |
0.6 |
|
Pus for culture and sensitivity |
91 |
9.8 |
|
Sputum culture |
415 |
44.8 |
|
Throat swab culture |
1 |
0.1 |
|
Urine culture |
120 |
12.9 |
|
Wound swab for culture |
83 |
9.0 |
|
Total |
927 |
100.0 |
Table 2: Distribution of bacteria type according to culture results
Type of Bacteria |
Culture Result I R S |
Total
|
P-value |
||
Acinetobacterbaumannii |
0 |
24 |
0 |
24 |
|
Acinetobacter species |
2 |
177 |
6 |
185 |
|
Alpha Hemolytic Streptococcus |
0 |
1 |
1 |
2 |
|
B-Hemolytic Streptococcus-Group-A |
0 |
1 |
0 |
1 |
|
B-Hemolytic Streptococcus-Group-D |
0 |
1 |
0 |
1 |
|
Citrobacter Spp |
2 |
1 |
2 |
5 |
|
Coagulase negative Staphylococci |
19 |
14 |
24 |
57 |
|
Enterobacter Spp |
2 |
0 |
1 |
3 |
|
Enterococcus Spp |
0 |
18 |
1 |
19 |
|
Escherichia coli |
7 |
159 |
60 |
226 |
|
Klebsiella pneumoniae |
10 |
60 |
29 |
99 |
|
Klebsiella Spp |
2 |
42 |
6 |
50 |
|
Moraxella Spp |
0 |
0 |
4 |
4 |
|
Methicillin Resistant Staphylococcus aureus(MRSA) |
6 |
11 |
0 |
17 |
0.001 |
Neisseria Spp |
0 |
0 |
1 |
1 |
|
Nocardia SPP |
0 |
0 |
1 |
1 |
|
Proteus mirabilis |
0 |
3 |
0 |
3 |
|
Proteus Spp |
2 |
6 |
2 |
10 |
|
Proteus vulgaris |
0 |
0 |
1 |
1 |
|
Pseudomonas aeruginosa |
11 |
52 |
49 |
112 |
|
Serratia Spp |
0 |
0 |
4 |
4 |
|
Staphylococcus aureus |
3 |
7 |
62 |
72 |
|
Streptococcus pneumoniae |
0 |
0 |
3 |
3 |
|
Streptococcus spp. |
2 |
3 |
22 |
27 |
|
Total |
68 |
580 |
279 |
927 |
|
Figure 2: Distribution of age group and sex according to Culture results
Table 3: Distribution of age group and sex according to Culture results
Variable |
Culture results |
Total |
P-value |
|||
|
I |
R |
S |
|
|
|
Sex |
F |
26 |
170 |
91 |
287 |
|
M |
42 |
410 |
188 |
640 |
0.25 |
|
Total |
68 |
580 |
279 |
927 |
|
|
Age group |
Less 20 |
14 |
62 |
48 |
124 |
|
21-40 |
12 |
134 |
67 |
213 |
0.02 |
|
41-60 |
13 |
170 |
78 |
261 |
||
60 |
29 |
214 |
86 |
329 |
|
|
Total |
68 |
580 |
279 |
927 |
|
Table 4: Distribution of culture results according to sample type
Sample Type |
Culture Result |
Total |
P-value |
||
|
I |
R |
S |
|
|
Ascitic fluid c/s and sensitivity |
0 |
0 |
1 |
1 |
0.001 |
Aspirated fluid culture |
0 |
8 |
14 |
22 |
|
Blood culture |
18 |
62 |
64 |
144 |
|
Cerepro Spinal Fluid (CSF) C/S |
0 |
14 |
3 |
17 |
|
General swab for culture |
2 |
18 |
7 |
27 |
|
Pleural fluid for culture and sensitivity |
0 |
1 |
5 |
6 |
|
Pus for culture and sensitivity |
6 |
31 |
54 |
91 |
|
Sputum culture |
28 |
308 |
79 |
415 |
|
Throat swab culture |
0 |
0 |
1 |
1 |
|
Urine culture |
7 |
83 |
30 |
120 |
|
Wound swab for culture |
7 |
55 |
21 |
83 |
|
Total |
68 |
580 |
279 |
927 |
|