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

ABSTRACT

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

  1. Lode H, Allewelt M. Role of newer fluoroquinolones in lower respiratory tract infections. J Antimicrobial Chemotherapy. 2002; 49: 709–712.
  2. Wise R, Honeybourne D. Pharmacokinetics and pharmacodynamics of fluoroquinolones in the respiratory tract. Europ Resp J. 1999; 221–9.
  3. Blondeau JM. Clinical utility of the new fluoroquinol- ones for treating respiratory and urinary tract infections. Expert Opinion on Investigational Drugs. 2002; 10, 213–36.
  4. Wiemken TL, Peyrani P, Ramirez JA. Global changes in the epidemiology of community-acquired pneumonia. Semin Respir Crit Care Med. 2012; 33:213–219.
  5. Welte T, Torres A, Nathwani D. Clinical and economic burden of community-acquired pneumonia among adults in Europe. Thorax. 2012; 67:71– 79.
  6. Kees MG, Weber S, Kees F, Horbach T. Pharmacokinetics of moxifloxacin in plasma and tissue of morbidly obese patients. J Antimicrob Chemother. 2011; 66:2330 –2335.
  7. Balfour JA, Lamb HM. Moxifloxacin: a review of its clinical potential in the management of community-acquired respiratory tract infections. Drugs. 2000; 59:115–139
  8. O¨ brink-Hansen K, Hardlei TF, Brock B, Jensen-Fangel S, Kragh Thomsen M, Petersen E, Kreilgaard M. Moxifloxacin pharmacokinetic profile and efficacy evaluation in empiric treatment of community-acquired pneumonia. Antimicrob Agents Chemother. 2015; 59:2398 –2404
  9. Niederman M, Church D, Haverstock M, Springsklee M. Does appropriate antibiotic therapy influence outcome in community-acquired pneumonia (CAP) and acute exacerbations of chronic bronchitis (AECB)? J Resp Med. 2000; Suppl. A, E23.
  10. Christina Krasemann, Jutta Meyer, Glenn Tillotson. Evaluation of the clinical microbiology profile of moxifloxacin. clinical infectious diseases. 2001; 32 (Suppl 1):S51–63.
  11. Tillotson G, Blondeau J. Today’s community respiratory tract infections: a challenge appropriate for moxifloxacin. In: Adam D, Finch R, eds. Moxifloxacin in practice. Oxford: Maxim Medical, 1999: 1–11.
  12. Gerald L. Murray, Catriona S. Bradshaw, Melanie Bissessor, Jennifer Danielewski, Suzanne M. Garland, Jørgen S. Jensen, Christopher K. Fairley, Sepehr N. Tabrizi. Increasing macrolide and fluoroquinolone resistance in Mycoplasma genitalium. Emerging Infectious Diseases. 2017; 23 (5).
  13. Dalhoff A. Global fluoroquinolone resistance epidemiology and implictions for clinical use. Inter discip Perspect Infect Dis. 2012; 2012:976273.
  14. Pillar CM, Thornsberry C, Sahm DF. “Susceptibility of Streptococcus pneumonia and Haemophilus influenza collected across Europe and Asia to levofloxacin and other respiratory agents; results from GLOBAL surveillance (1997–2007),” Penetration, 2010; 14–22.
  15. Ali I, Butt MA. Antibiotic susceptibility pattern of bacterial isolates from patients of respiratory tract infection at 43 centers in Punjab, Pakistan. Clin Exp Pharmacol. 2017; 7: 229.
  16. Anderson H, Esmail A, Hollowell J, Littlejohns P, Strachen D. Epidemiologically based needs assessment: lower respiratory disease. DHA Project Research Prograrnme. 1993; 6-12.

 

 

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