Boditech Interleukin-6

Interleukin-6

The earliest alarming for sepsis

Every minute and every second, the medical team had always encountered challenges. The clinicians kept thinking about how to detect a baby’s condition earlier and how to reduce antibiotics administration. Interleukin-6 acts as a pro-inflammation cytokine and a key mediator of inflammation. During the acute phase of infection, B and T lymphocytes are stimulated to produce the Interleukin-6 cytokine, which in turn induces hepatocyte production of acute-phase reactants such as CRP.

With these characteristics, the Interleukin-6 could help to detect EOS(Early Onset Sepsis) earlier and can work as a complementary function with existing tests such as CRP(C-Reactive Protein) and PCT(Procalcitonin). Boditech Med has launched the AFIAS Interleukin-6 in September 2020, and it has been landed successfully. It is expected that the AFIAS Interleukin-6 test aid to detect inflammation in the early stage and will contribute to improving the newborn’s health.

 

Interleukin-6, an essential test for NICU and children’s hospital

1. Early Onset Sepsis occurs within 72 hours of life

Neonatal sepsis is a major contributor to morbidity and mortality in neonates, especially in those born preterm. The Global Burden of Disease (GBD) estimated 1.3 million annual incident cases of neonatal sepsis and other infections 2,874 sepsis cases per 100,000 live births and a mortality of 17.6%.

2. Exposure to inappropriate and/or excessive antibiotic use

Antibiotics are the most commonly prescribed class of medications in the NICU. The probability of EOS combined with the clinical instability characteristic of premature newborns leads to high rates of empirical antibiotic treatment. previous studies demonstrate that neonatal clinicians administer antibiotics from birth in 79% to 98%.

3. C-tip is the ideal method for infants’ or children’s sample collection

An infant’s blood collection cannot exceed 1% of body blood, usually premature baby is under 2 kg therefore, 1 ml for once is maximum. The research shows, that 51.7% of hospitals in Korea collect 0.5 ml, and 24.1% collect 1 ml from an infant’s heel for a blood culture test. It is already in the dangerous range for infants.

NICU clinicians need the method to improve diagnostic capabilities, which can provide reliable results, early and rapid, simple and safely in the patient’s bedside or in the ICU.

AFIAS parameters

ichroma parameters

Liofilchem Microbiology products (Antimicrobial resistance management)

MTS™ Synergy Application System
for in-vitro combination of antibiotics

Antimicrobial resistance is a major challenge for clinicians and clinical microbiologists, and the use of synergy testing is nowadays increasingly requested.

MTS-SAS combines the reliability of MIC Test Strip with patented tools to facilitate and standardize a critical assay such as the in-vitro combination of antibiotics.

MTS-SAS procedure is significantly faster than any other methods in antibiotic synergy tests (i.e. time-kill, checkerboard), does not require any additional training to those who are skilled in the usage of MIC Test Strip, reduces or eliminates the risks of procedure errors when compared to laborious and complicated traditional methods:

• standardized
• easy to use
• save time, materials, workload, resources

 

 

Individually packed, gamma-irradiated contact plates

The peelable blister pack fulfils the highest quality and protection standards for the plate.
The blister pack, fully automatically produced in a controlled environment, delivers the following benefits:

individual plate packaging;
clear package transparency;
drastically reduces the dehydration of culture media during the shelf life period;
up to 9 months shelf-life;
storage at ambient temperature for most of the items in its range;
reduces contamination risks in controlled environments;
available as gamma-irradiated, triple-enveloped plates, suitable for restricted areas such as isolators and clean rooms.

 

Liofilchem Microbiology products

(New) Fastidious Anaerobe Agar (FAA)

Fastidious Anaerobe Agar (catalogue ref. 10062) is a ready-to-use agar plate for the cultivation and

antimicrobial susceptibility testing of anaerobic bacteria. This medium is recommended by the European Committee on Antimicrobial Susceptibility Testing (EUCAST) for disk diffusion of selected rapidly growing anaerobic bacteria, i.e. Bacteroides spp., Prevotella spp., Fusobacterium necrophorum, Clostridium perfringens and Cutibacterium acnes.

FAA permits excellent growth of most anaerobic bacteria and is the medium chosen by EUCAST for the development of a disk diffusion method for anaerobes.

FAA plates are inoculated with a bacterial suspension in 0.85% saline from overnight cultures, adhering to the 15-15-15-minute rule (suspension used within 15 minutes, disks applied within 15 minutes of inoculation, and incubation within 15 minutes of applying the disks). The antibiotic disks are applied to the agar surface. Plates are incubated in an inverted position at 36 ± 1°C for 16-20 hours in an anaerobic atmosphere (80% N2, 10% H2, 10% CO2).

At the end of the incubation period, the inhibition zone diameters are measured and interpreted according to the current EUCAST breakpoints and QC criteria for disk diffusion of anaerobes. Refer to the current EUCAST disk diffusion reading guide for anaerobic bacteria.

Ref. 10062
90 mm plates, 20/pack
2 months shelf life
2-8°C storage temperature

 

Enterosystem 18R

Biochemical identification of Gram-negative, oxidase-negative Enterobacteria

Enterosystem 18R is an 18-well system containing desiccated biochemical substrata for the identification of Gram-negative, oxidase negative enterobacteria. The system is inoculated with the suspension of the organism and incubated at 36±1°C for 12-18-24 hours. The microorganism is then identified by assessing the colour change in the wells to determine the corresponding numerical code. A codebook or the online Identification Code Disk allow for the microbial ID.

Ref. 71618
90 panels/pack
16 months shelf life
2-8°C storage temperature

 

Steel Coupons

for hydrogen peroxide sterilization

Biological indicators OXI CONTROL GST E6/E5/E4/E3/E2 SS are used for regular control of H2O

 

2 vapour superficial decontamination cycles and validation of sterilizers. These biological indicators use a stainless-steel support (coupon), that is not permeable to hydrogen peroxide. Stainless-steel coupon has been inoculated with

Geobacillus stearothermophilus ATCC® 7953 spores and has been introduced into a Tyvek®/Polytene envelope. Tyvek® side of the envelope is permeable to hydrogen peroxide vapour, while the Polytene side of the envelope is not permeable to these vapours. Biological indicators OXI CONTROL GST E6/E5/E4/E3/E2 are produced under strictly controlled conditions to satisfy the requirements indicated in the USP and EP current editions and accordance with ISO 11138 and EN 866 standards.

 

ref. 91082

20 coupons + 20 tubes
2-8°C storage temperature
3 years shelf life

 

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