Rapid Diagnostic Panel Used for Pediatric Musculoskeletal Infections
|
By LabMedica International staff writers Posted on 31 Jul 2019 |

Image: The Xpert MRSA/SA SSTI assay detects methicillin-resistant S. aureus (MRSA) & S. aureus (SA) in skin and soft tissue infections in less than one hour (Photo courtesy of Cepheid).
The findings from a retrospective analysis suggested that the use of a rapid musculoskeletal diagnostic panel, or MDP, could have shortened the time it took to identify the cause of infection, provide appropriate antibiotics and reduce the length of stay for children in hospital.
The MDP, which was recently validated in another study, combined three separate tests: the Xpert MRSA/Staphylococcus aureus skin and soft tissue infection (SA SSTI) assay, a polymerase chain reaction (PCR) assays for ermA, ermB and ermC genes to determine clindamycin resistance; and a Kingella kingae PCR assay to identify the rtxA gene. Results from the Xpert MRSA/SA SSTI assay were available within three hours, and results for the PCR assays were available by 1400 hours the following calendar day.
Scientists at the Children’s Hospital Colorado (Aurora, CO, USA) included in a study 53 children aged six months to 18 years who were admitted to the hospital with symptoms persisting for less than two weeks, had bone or joint specimens collected and were administered antibiotic therapy, excluding perioperative antibiotics. The investigators identified pathogens in 69.8% of patients (37/53) who underwent standard culturing techniques and in 13 patients (16%) who had a blood culture performed. The most commonly identified pathogen was S. aureus (47.2%), and methicillin-resistant S. aureus (MRSA) was identified in 16% of these patients. Two patients had clindamycin-resistant S. aureus, and one patient had a K. kingae infection.
The MDP identified most children with culture-confirmed S. aureus infection (88%), with three patients having MRSA. When cultured, all three patients were confirmed to have MRSA. Although the MDP identified three isolates as clindamycin resistant, culture showed that one of these isolates was clindamycin susceptible. The results showed that MDP would have saved seven hours to pathogen identification (45.6 hours; interquartile range [IQR] = 23-62) compared with standard microbiology culture techniques (52.5 hours; IQR = 36.1-65.6). Additionally, use of the MDP would have improved the time to definitive antibiotic therapy by nearly 22 hours and reduced the hospital length of stay by a median of 26.4 hours.
The authors noted that cost is an important factor when considering a new diagnostic tool like the MDA. Theoretically, the decrease in length of stay would justify its expense. Justin B. Searns, MD, a hospitalist and first author of the study, said, “No approved rapid diagnostic platforms currently exist for bone and joint specimens from pediatric patients with acute musculoskeletal infection.” The study was published on June 13, 2019, in the Journal of The Pediatric Infectious Disease Society.
Related Links:
Children’s Hospital Colorado
The MDP, which was recently validated in another study, combined three separate tests: the Xpert MRSA/Staphylococcus aureus skin and soft tissue infection (SA SSTI) assay, a polymerase chain reaction (PCR) assays for ermA, ermB and ermC genes to determine clindamycin resistance; and a Kingella kingae PCR assay to identify the rtxA gene. Results from the Xpert MRSA/SA SSTI assay were available within three hours, and results for the PCR assays were available by 1400 hours the following calendar day.
Scientists at the Children’s Hospital Colorado (Aurora, CO, USA) included in a study 53 children aged six months to 18 years who were admitted to the hospital with symptoms persisting for less than two weeks, had bone or joint specimens collected and were administered antibiotic therapy, excluding perioperative antibiotics. The investigators identified pathogens in 69.8% of patients (37/53) who underwent standard culturing techniques and in 13 patients (16%) who had a blood culture performed. The most commonly identified pathogen was S. aureus (47.2%), and methicillin-resistant S. aureus (MRSA) was identified in 16% of these patients. Two patients had clindamycin-resistant S. aureus, and one patient had a K. kingae infection.
The MDP identified most children with culture-confirmed S. aureus infection (88%), with three patients having MRSA. When cultured, all three patients were confirmed to have MRSA. Although the MDP identified three isolates as clindamycin resistant, culture showed that one of these isolates was clindamycin susceptible. The results showed that MDP would have saved seven hours to pathogen identification (45.6 hours; interquartile range [IQR] = 23-62) compared with standard microbiology culture techniques (52.5 hours; IQR = 36.1-65.6). Additionally, use of the MDP would have improved the time to definitive antibiotic therapy by nearly 22 hours and reduced the hospital length of stay by a median of 26.4 hours.
The authors noted that cost is an important factor when considering a new diagnostic tool like the MDA. Theoretically, the decrease in length of stay would justify its expense. Justin B. Searns, MD, a hospitalist and first author of the study, said, “No approved rapid diagnostic platforms currently exist for bone and joint specimens from pediatric patients with acute musculoskeletal infection.” The study was published on June 13, 2019, in the Journal of The Pediatric Infectious Disease Society.
Related Links:
Children’s Hospital Colorado
Latest Microbiology News
- Proteomic Workflow Maps Microbial and Host Responses in Intestinal Inflammation
- Metagenomic Sequencing Enables Faster Diagnosis of Respiratory Infections in Cystic Fibrosis
- Portable Molecular Platform to Advance Point-of-Care Testing for Lassa Fever
- New Sensitive Blood Assay Detects Tuberculosis Antigen Directly in Blood
- Study Highlights Need for Routine Hepatitis E Testing in Cirrhosis
- High-Throughput Automated Platform to Advance Latent Tuberculosis Testing
- Expanded Diagnostics and Therapies Target Rising Gonorrhea Resistance
- New Rapid Ebola Antigen Test Detects Infection at Point of Care
- Syndromic GI Panel Detects Cyclospora for Rapid Case Confirmation
- Rapid Panel Identifies Gram-Negative Pathogens and Resistance Markers in Bloodstream Infections
- Bacterial Growth Assay Predicts COVID-19 Severity From Plasma
- Gut Microbiome Analysis Identifies Frailty-Related Signatures in Older Adults
- CE-Marked Blood Assay Automates Tuberculosis Infection Testing
- Genomic Surveillance Algorithm Improves Early Detection of Emerging Variants
- Rapid Gastrointestinal PCR Panels Deliver One-Hour Results
- H. pylori Screening Within Colorectal Program Aids Gastric Cancer Prevention
Channels
Clinical Chemistry
view channel
Blood Biomarker Reveals Hidden Disability Progression in Multiple Sclerosis
Multiple sclerosis (MS) remains difficult to monitor because neurological decline can continue even after relapses stop. This progression independent of relapse activity is often subtle and may escape... Read more
Blood Test Enters UK Primary Care Pathway for Earlier Alzheimer’s Diagnosis
Alzheimer’s disease is often first suspected in primary care, yet definitive evaluation frequently depends on specialized imaging or cerebrospinal fluid testing. This creates a persistent gap between disease... Read moreMolecular Diagnostics
view channel
Single Liquid Biopsy Predicts Early Immunotherapy Benefit in Advanced Lung Cancer
Assessing early benefit from immunotherapy in advanced non-small cell lung cancer can be challenging because radiographic responses may take months to become clear. Early scans can also be difficult to... Read more
Machine Learning Tool Improves Prediction of Liver Cancer Recurrence
Recurrent hepatocellular carcinoma (HCC) after surgery remains a major cause of poor outcomes and contributes to liver cancer’s rank as the world’s third leading cause of cancer death. The burden is particularly... Read moreHematology
view channel
Age-Specific CBC Reference Intervals Support Pediatric Diagnosis in Vietnam
Complete blood count (CBC) results underpin pediatric evaluation for anemia, infection, inflammation, and platelet disorders. Yet laboratories in Vietnam have largely relied on reference intervals derived... Read more
Spectral Flow Cytometry Assay Enhances MRD Detection in Multiple Myeloma
Minimal residual disease (MRD) monitoring is pivotal in multiple myeloma, where persistent malignant plasma cells drive relapse risk and help guide therapy decisions. In the United States, approximately... Read moreImmunology
view channel
Study Reveals Immune Mechanism Driving Severe COVID-19 Progression
Severe COVID-19 has highlighted gaps in understanding of early antiviral responses, particularly why some patients deteriorate despite timely care. Type I interferons are central to host defense, yet their... Read more
Antibody Profiling Identifies Preclinical Inflammatory Bowel Disease Years Before Diagnosis
Inflammatory bowel disease often develops after a prolonged symptom-free period, complicating timely recognition and clinical intervention. Limited understanding of immune activity during this silent phase... Read more
Ultrasensitive Blood Test Detects Sjögren’s Signature Years Before Diagnosis
Sjögren’s disease is a common autoimmune condition that can be difficult to recognize early, leading to delayed diagnosis and persistent symptom burden. It affects around half a million people in the UK... Read more
New Assays Expand Cytokine Testing for Transplant and Immunocompromised Patients
Eurofins Viracor has introduced three plasma-based assays—CXCL9 (Test Code 33607), CXCL10 (Test Code 33609), and interleukin-18 (IL-18) (Test Code 33611)—expanding its immunology testing menu for transplant... Read morePathology
view channel
AI Pathology Tool Predicts Relapse Risk in Stage II Colorectal Cancer
Bowel cancer is Australia’s fourth most commonly diagnosed cancer and the second leading cause of cancer death, while remaining the third most common cancer worldwide. In stage-two disease, determining... Read more
AI Pathology Tool Stratifies Rectal Cancer to Guide Chemoradiotherapy
Choosing intensified regimens for locally advanced rectal cancer is challenging because these therapies can cause serious side effects. Colorectal cancer is the fourth-most fatal cancer in the UK, and... Read more
PD-L1 Assay Guides Pembrolizumab Eligibility in Ovarian, Fallopian Tube, and Peritoneal Cancers
Agilent Technologies’ PD-L1 IHC 22C3 pharmDx (Code SK006) has received European Union certification as a companion diagnostic to aid in identifying patients with epithelial ovarian, fallopian tube, or... Read moreTechnology
view channel
Interoperable Data Platform Standardizes Multi-Cancer Blood Test Results
Proteotype Diagnostics has introduced Alchemi, a proprietary data and clinical workflow platform being developed for Enlighten, the company’s investigational blood-based multi-cancer test.... Read more
Training Device Improves Accuracy of Pooled Molecular Diagnostics
High-throughput molecular diagnostics have transformed infectious disease detection, but many workflows remain difficult to execute accurately without extensive training. Sample pooling can cut per‑test... Read more
New CE-Certified Software Advances Whole-Genome Cancer Testing
European hospitals are increasingly using comprehensive tumor genomics to guide therapy, but routine whole genome sequencing (WGS) requires validated, regulation-compliant workflows. A newly CE-certified... Read more
National Rare Disease Registry Standardizes Genetic and Clinical Data for Coordinated Care
Rare diseases collectively impose a significant clinical burden despite their individual rarity, often involving multisystem presentations and prolonged diagnostic journeys. Limited specialist expertise... Read moreIndustry
view channel
Global Testing Service Advances Leukemia MRD Monitoring
KMT2A rearrangements drive aggressive subsets of acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) and are associated with relapse and poor outcomes. As menin inhibitors enter clinical... Read more







