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Paediatric colistin prescribing practices in South Africa: A clinician survey
Veshni Pillay-Fuentes Lorente1, Trusha Nana2,3, Marianne Black2,4
1Division of Clinical Pharmacology, Department of Medicine, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Insights
This study surveyed South African doctors on pediatric colistin use, finding varied dosing practices. A new guideline aims to standardize colistin prescribing for children in South Africa.
Area of Science:
- Pharmacology
- Infectious Diseases
- Pediatrics
Background:
- Multidrug-resistant bacterial infections pose a global health threat.
- Colistin is a last-line treatment for resistant Gram-negative pathogens.
- Paediatric colistin prescribing guidelines are currently lacking.
Purpose of the Study:
- To investigate paediatric colistin prescribing practices in South Africa.
- To identify challenges in paediatric colistin use.
- To inform the development of a paediatric colistin guideline.
Main Methods:
- An anonymous online survey was distributed to medical practitioners in South Africa.
- The survey focused on colistin prescribing for patients aged 14 years and younger.
- Data on dosing, empiric use, and perceived needs were collected.
Main Results:
- Varied loading and maintenance doses of colistin were reported.
- Nearly half of the respondents used colistin empirically, with many continuing it for over 72 hours.
- High perceived need for readily available therapeutic drug monitoring was noted.
Conclusions:
- Paediatric colistin prescribing practices in South Africa are diverse.
- A new evidence-based paediatric colistin guideline has been published.
- Future research will assess the guideline's impact on prescribing practices.
Background:
Increasing multidrug-resistant bacterial infections are a global health challenge. Colistin, a polymyxin antimicrobial, has activity against some resistant strains, and despite its adverse effects, it presents a last-line option to treat resistant Gram-negative pathogens. However, paediatric colistin prescribing guidelines are lacking.
Objectives:
To determine paediatric colistin prescribing practices and challenges in South Africa (SA) to aid the development of a paediatric colistin guideline.
Method:
We conducted an anonymous online survey of registered medical practitioners in SA who prescribed colistin to patients aged ≤ 14 years in the past 12 months.
Results:
Of 196 participants, 71.9% (n = 141/196) completed the survey. Eighty-six respondents (n = 86/146; 58.9%) reported prescribing loading doses (LD), with the median LD and maintenance doses of 150 000 IU/kg/dose (interquartile range (IQR), 75 000-150 000) and 50 000 IU/kg/dose (IQR, 40 000-50 000), respectively. Empiric colistin use was reported by 47.2% (n = 69/146), of whom 46.3% (n = 32/69) continued empiric colistin for ≥ 72 h. Using the Likert scale, respondents highly perceived that therapeutic drug monitoring should be readily available (mean = 3.97). The perception that prescribing colistin should be advised by a microbiologist or infectious disease specialist had a mean score of 2.97, indicating moderate agreement.
Conclusion:
This survey demonstrated varied paediatric colistin prescribing practices. Recently, a new evidence-based paediatric guideline for colistin use in SA has been published. A follow-up survey will be conducted to assess the impact of the guideline on paediatric colistin prescribing practices in SA.
Contribution:
This study highlighted paediatric colistin dosing practices in the absence of a paediatric colistin guideline in South Africa.
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