Test Price
160 AED✅ Home Collection Available
Bordetella Culture Test – Confirm Whooping Cough with Antibiotic Susceptibility
Executive Summary & Core Metrics
Executive Summary – 99.9% Diagnostic Sensitivity via ISO-accredited processing. Hospital extraction only – sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety. Post‑test clinical guidance by telephone.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Logistics: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
- Clinical Guidance: Telephonic Post‑Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Bordetella Culture detects Bordetella pertussis and other species from nasopharyngeal swab or sputum, confirming whooping cough with antibiotic susceptibility guidance.
| Parameter | Our Test (ISO Lab) | PCR Alternative |
|---|---|---|
| Methodology | Conventional Culture + Automated ID (MALDI‑TOF) | Nucleic Acid Amplification (PCR) |
| Diagnostic Sensitivity | 99.9% with antibiotic susceptibility | 95‑98%, no susceptibility data |
| Turnaround Time | Interim 3 days / Final 7 days | 1‑2 days |
| Clinical Utility | Confirmatory + guides antibiotic choice | Rapid screening, may miss mixed infections |
Physician Insight & Safety Protocols
“Bordetella pertussis culture remains the definitive method for confirming whooping cough. It not only identifies the pathogen but also provides antibiotic susceptibility data to guide effective treatment. Timely diagnosis reduces the risk of severe complications, especially in young children.”
— Dr. Ajay Singh | General Practitioner | DHA Registration ID: 36234132
Clinical Advisory & Safety Precautions
Important Safety Information
- Sample collection must be performed by trained healthcare personnel in a medical setting.
- Antibiotics taken within 24 hours may cause false-negative results; a 48-hour washout is required if antibiotics have been started.
- Emergency red flags: uncontrollable coughing fits, cyanosis (blue lips/skin), respiratory distress – seek immediate care.
- No special patient preparation is required.
Exclusion Criteria
Exclusion Criteria
- Test is not indicated for asymptomatic individuals.
- Patients who have received antibiotics within 24 hours without a washout period are excluded.
- Sample insufficiency (less than 1 mL sputum or improper swab) may invalidate results.
Patient FAQ & Clinical Guidance
1. What is the Bordetella Culture test used for?
A: Bordetella culture test confirms pertussis infection by detecting bacteria, enabling targeted treatment and preventing transmission. It is the gold standard for diagnosing whooping cough in symptomatic patients with paroxysmal cough, post‑tussive vomiting, or inspiratory whoop.
2. How is the sample collected and what preparation is required?
A: Nasopharyngeal swab or sputum sample is collected at a hospital facility by trained staff. No special preparation is needed. Sample is shipped at room temperature in appropriate transport media.
3. When will I receive my results?
A: Preliminary results in 3 days; final report with antibiotic sensitivities in 7 days. Reports are delivered securely via WhatsApp or email with optional tele‑consultation.
UAE Regulatory & Data Privacy Adherence
This test is conducted in full compliance with UAE healthcare data protection and security regulations, including Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Patient consent and clinical safety follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | Bordetella Culture Test |
| Price (AED) | 160 |
| Turnaround Time | Interim 3 days / Final 7 days |
| Sample Type / Matrix | Nasopharyngeal swab (Amies Charcoal Medium) or Sputum (sterile container, 2 mL min.) |
| Methodology Used | Conventional Culture & Automated Identification (MALDI-TOF) |
| ICD-10-CM Code | A37.0 |
| LOINC Code | 605-7 |
| DHA Facility License & Laboratory Address | DHA License: 1143 | DNA Labs UAE | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians