# Results from the Survey of Antibiotic Resistance (SOAR) 2018–21 in Kuwait and the United Arab Emirates: data based on CLSI, EUCAST (dose-specific) and pharmacokinetic/pharmacodynamic (PK/PD) breakpoints

**Authors:** Didem Torumkuney, Eiman Mokaddas, Stefan Weber, Ian Morrissey, Nergis Keles, Anand Manoharan

PMC · DOI: 10.1093/jac/dkaf284 · Journal of Antimicrobial Chemotherapy · 2025-11-24

## TL;DR

This study analyzed antibiotic resistance in respiratory tract bacteria from Kuwait and UAE, showing high susceptibility to fluoroquinolones and lower to penicillin and other drugs.

## Contribution

The study provides region-specific antibiotic susceptibility data using multiple breakpoint standards for S. pneumoniae and H. influenzae.

## Key findings

- Fluoroquinolones showed ≥98% susceptibility in pneumococci across both regions.
- Penicillin susceptibility was low (20%–27%) using CLSI oral/EUCAST low-dose breakpoints.
- H. influenzae in Kuwait had lower susceptibility to trimethoprim/sulfamethoxazole (47.1%) compared to UAE (55.7%).

## Abstract

To determine antibiotic susceptibility of Streptococcus pneumoniae and Haemophilus influenzae from community-acquired respiratory tract infections in Kuwait and United Arab Emirates (UAE), collected in 2018–21.

MICs determined by CLSI broth microdilution; susceptibility data interpreted using CLSI and EUCAST breakpoints.

A total of 49 S. pneumoniae and 79 H. influenzae and 49 S. pneumoniae and 34 H. influenzae were collected from Kuwait and UAE, respectively. Of the pneumococci, 26.5% (UAE) and 20.4% (Kuwait) were penicillin susceptible by CLSI oral/EUCAST low-dose breakpoints; by CLSI intravenous/EUCAST high-dose administration, 95.9% (UAE) and 85.7% (Kuwait) were susceptible. Similar susceptibility was observed to ceftriaxone, amoxicillin/clavulanic acid, amoxicillin and cefotaxime (CLSI: 73.5%–93.9%) but lower to other cephalosporins, tetracyclines, macrolides and trimethoprim/sulfamethoxazole. Fluoroquinolones were ≥98.0% susceptible (CLSI/EUCAST high-dose). Compared with CLSI, activity was similar by EUCAST high-dose or pharmacokinetic/pharmacodynamic (PK/PD) breakpoints with few exceptions. Of the H. influenzae isolates, 17.7% (Kuwait) and 8.8% (UAE) carried β-lactamases. Significant differences in H. influenzae susceptibility (CLSI) were found for amoxicillin/clavulanic acid (81.0% Kuwait/97.1% UAE) and fluoroquinolones (UAE: levofloxacin 88.2%, moxifloxacin 82.4%; Kuwait: both 98.7%). Susceptibility was overall >91.2% (CLSI) except for ampicillin (81.0% Kuwait) and trimethoprim/sulfamethoxazole (47.1% UAE/55.7% Kuwait). EUCAST susceptibility was similar, except for cefuroxime. PK/PD susceptibility was similar to CLSI, but lower for cefaclor, cefuroxime and macrolides.

Pneumococci were susceptible to fluoroquinolones (>98%), amoxicillin and amoxicillin/clavulanic acid (>79%–94%), ceftriaxone and cefotaxime (>73%–94%). Susceptibility was lower to oral/low-dose penicillin (20%–27%), macrolides (33%–51%), tetracyclines (53%–59%) and trimethoprim/sulfamethoxazole (33%–61%). Susceptibility was generally >80% in H. influenzae except for trimethoprim/sulfamethoxazole (47%–56%).

## Linked entities

- **Chemicals:** penicillin (PubChem CID 2349), ceftriaxone (PubChem CID 5479530), amoxicillin/clavulanic acid (PubChem CID 6435924), amoxicillin (PubChem CID 33613), cefotaxime (PubChem CID 5742673), trimethoprim/sulfamethoxazole (PubChem CID 358641), levofloxacin (PubChem CID 149096), moxifloxacin (PubChem CID 152946), cefuroxime (PubChem CID 5479529), cefaclor (PubChem CID 51039), ampicillin (PubChem CID 6249)
- **Species:** Streptococcus pneumoniae (taxon 1313), Haemophilus influenzae (taxon 727)

## Full-text entities

- **Diseases:** respiratory tract infections (MESH:D012141)
- **Chemicals:** cefotaxime (MESH:D002439), ampicillin (MESH:D000667), levofloxacin (MESH:D064704), amoxicillin/clavulanic acid (MESH:D019980), moxifloxacin (MESH:D000077266), penicillin (MESH:D010406), trimethoprim/sulfamethoxazole (MESH:D015662), ceftriaxone (MESH:D002443), macrolides (MESH:D018942), amoxicillin (MESH:D000658), cephalosporins (MESH:D002511), cefuroxime (MESH:D002444), cefaclor (MESH:D002433), Fluoroquinolones (MESH:D024841), tetracyclines (MESH:D013754)
- **Species:** Streptococcus pneumoniae (species) [taxon 1313], Haemophilus influenzae (species) [taxon 727]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12641136/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12641136/full.md

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Source: https://tomesphere.com/paper/PMC12641136