A burn injuries

Interpretation Exercise

Burn injuries are most often caused when your skin comes in immediate connection with a naked flame or a hot surface. Scalding may appear when you can find contact with a hot water. There are several other types of burns such as chemical substance, induced by strong acids or bases, and rays, the common example being sunburn from UV light.

Burns are labeled by level, where severity heightens with a higher degree. A more recent classification system separates uses up into three categories: superficial, incomplete width and full width burns. The individual in the scenario has a complete thickness third level shed. This usually brings about lack of the outer skin layer (epidermis) leading to the patient's skin to be numb and feel hard and leathery to touch. This amount of melt away requires immediate medical attention as they do not heal independently. Proteins at the website of injury denature and skin cells eventually die, designated by the forming of black eschar at the centre of the wound. After the skin barrier has been damaged, the homeostatic functions of the skin are lost. You can find rapid lack of body substance and bloodstream plasma which will often cause visible swelling.

As the skin is the body's first line of defence, lose wound infections correlate with how big is the burn damage. The skin constantly sheds off and will take harmful bacteria with it. Furthermore, the acidic character of the skin prevents the entrance of microorganisms that generally like neutral conditions. Melts away are also associated with a depressed immune response. With all this information, it is no surprise that an infection is the principal cause of fatality in burn off victims. As it is a third degree burn, the individual will have put in time in clinic where there is a greater risk of infection. Patient to patient contact via hospital equipment and personnel allows rapid transmitting of pathogenic bacterias. The melt away wound is a favourable site for opportunistic colonization by pathogens because the eschar offers a moist, protein enhanced environment which encourages bacterial growth. The excess of necrotic tissue provides a wealthy development medium for the microorganism.

In the clinical presentation, the patient complained of fever, chills and a distressing smelling discharge from the shed wound. These are all signs or symptoms of infection therefore the doctor was right to prescribe the individual an antibiotic. However, on the basis of the array of microbiology data collected in the lab, the doctor's selection of antibiotic was incorrect. A bi weekly course of flucloxacillin 500mg was recommended to the patient to be taken orally 4 times daily. Flucloxacillin can be an antibiotic belonging to the penicillin group. It can be used to treat attacks induced by gram-positive bacteria, mostly Staphylococcus aureus. In the lab, the microscopic slip was reviewed under a microscope using the olive oil immersion lens. Fishing rod molded microorganisms were detected and they were stained a red/red colour. This indicates the bacteria within the pus samples is gram negative. Therefore, flucloxacillin could have no therapeutic effect to the individual as it is merely bactericidal against gram-positive cells.

The three agar plates were evaluated and observations on the colour, shape, size and smell of the colonies was observed. There was no visible progress on the Mannitol salt agar (MSA) plate. This sort of selective agar can be used to isolate Staphylococcus aureus as it inhibits almost every other bacteria because of its high sodium chloride attention (7. 5 %w/v). The absence of growth on the MSA plate provides further data that there surely is no Staphylococcus aureus colonisation in the patient.

The colonies on the cetrimide agar were a pale, cloudy brown colour and gave from the smell of rotting fruit. The usage of cetrimide agar as a selective and differential agar permits the isolation of Pseudomonas aeruginosa, a gram-negative microorganism. Cetrimide can be an ammonia mixture which inhibits most bacterias, including some Pseudomonas kinds (however, not P. aeruginosa). It also enhances production of the pigment pyocyanin which results in glowing inexperienced colonies. However, some strains of P. aeruginosa do not produce the pigment. The growth on this plate proved the pathogen present in the patient is Pseudomonas aeruginosa and the colourless colonies indicate this can be a non-pigment producing stress.

There was also growth on the MacConkey agar where the colonies were somewhat colourless but experienced an orange tinge. MacConkey agar is a selective differential medium used to recognize gram-negative bacteria and determine whether they are lactose fermenters. Fermenters appear as scarlet colonies whilst non-fermenters are relatively colourless. As there is growth on this plate, the microorganism is unquestionably gram-negative however, not a fermenter due to the absence of red colonies. P. aeruginosa will not ferment lactose which clarifies the colour of the colonies.

An oxidase test was completed which gave a positive result, indicated by the deep blue color at the end of the test stick. An oxidase positive microbe possesses the enzyme required in the ultimate level of respiration to create metabolic drinking water. Only aerobic or facultatively anaerobic microorganisms give a positive final result. This biochemical test presents further proof that P. aeruginosa is the problem causing bacteria because it is an obligate aerobe and for that reason own the cytochrome oxidase enzyme.

Broth bottles comprising growth medium, a bacterial culture and an antibiotic at five different concentrations (all in g/ml) were seen. Cloudy broth dilutions mentioned the bacteria was immune and could grow. Clear broth dilutions revealed the bacteria was sensitive to the antibiotic and its own growth was inhibited. The bacterias was tolerant to erythromycin whatsoever concentrations used (1. 25-20g/ml). Erythromycin is a macrolide antibiotic related to penicillin. The results show it would haven't any therapeutic impact if recommended to the patient. Amoxicillin exhibited antimicrobial activity from the microorganism at concentrations of 20g/ml and 40g/ml. However, at concentrations above 12g/ml, the bacterium is known as resistant to amoxicillin so that it has no restorative effect to the patient. Penicillin's do not seem to own significant antimicrobial effects because of this pathogen which shows the doctor was wrong in his prescription of flucloxacillin as it is too a member of the penicillin group. The medication dosage of 500mg will unlikely be high enough to be beneficial and any therapeutic dosages would be at too much a concentration and for that reason impractical.

Cefuroxime, a second technology cephalosporin, was able to concentrations of 16g/ml and 32g/ml. Again, this was above the intermediate attentiveness range so does not benefit the patient. A newer technology cephalosporin might need to be utilized as they offer coverage against a broader spectral range of bacterias. The broth dilution formulated with ticarcillin was clear at concentrations of 8g/ml and 16g/ml. The intermediate focus range for this medication is 10-20g/ml so the minimum inhibitory amount is 8g/ml. This medication is a carboxypenicillin - a sub group of the penicillin family. The bacteria showed moderate awareness to the drug but only at quite high concentrations. Amikacin was also effective below its intermediate range (6-10g/ml) and inhibited bacterial progress at concentrations of 4g/ml, 6g/ml and 8g/ml. Amikacin is an aminoglycoside which is the right antibiotic to utilize from this pathogen as it exhibited high awareness to the medicine.

The doctor's selection of antimicrobial therapy will never be beneficial to the individual as flucloxacillin works well against gram-positive bacteria only and the patient is attacked with gram-negative P. aeruginosa. Unnecessary use of this antibiotic might lead to bacterial level of resistance. P. aeruginosa is naturally resistant to an array of antibiotics and so infections where it's the causative agent can be difficult to take care of. Broad-spectrum agents are essential as they are the only real drugs which provide coverage resistant to the bacteria. The individual could be cared for with an aminoglycoside such as amikacin. Gentamicin may be used but the experimental data shows the pathogen is obviously very sensitive to amikacin and studies have discovered that P. aeruginosa is more likely to develop resistance to gentamicin than amikacin. Aminoglycosides are bactericidal and take action by interfering with the bacterial ribosome, leading to wrong reading of messenger RNA. This might be used along with a third era cephalosporin such as ceftazidime. Carboxypenicillins may be used (e. g. ticarcillin) but they have only modest activity against Pseudomonas types and research has shown that bacteria quickly develop amount of resistance to them. Third era cephalosporins provide coverage against P. aeruginosa, unlike 1st and 2nd era which have a more limited spectral range of activity. Also, they are bactericidal and exert their effect by interfering with cell wall structure synthesis. Although there is absolutely no significant evidence of the huge benefits to using the two drugs in combination, it is rational to take action as it inhibits the emergence of mutant genes resistant to 1 of the realtors. Both drugs are also considered to have a synergistic impact when used jointly. Neither of the drugs are assimilated via the gastrointestinal area so must be administered via the parenteral option. Amikacin is given via intramuscular shot at a dosage of 15mg/kg daily in two divided doses. The dose must be chosen carefully as high degrees of amikacin in the bloodstream can damage the ear (ototoxicity). Ceftazidime is distributed by intravenous infusion at a dosage of around 2g every 12 hours, depending on the severity of the problem.

In synopsis, the available microbiology data indicates that the doctor's presumptive examination was incorrect and that the patient has a melts away infection induced by Pseudomonas aeruginosa. The lack of growth on the MSA dish disproved the thought of a staph aureus related infections. Gram-negative rods detected on the slip and expansion on the MacConkey agar clarified that the microorganism was gram-negative. Progress on the cetrimide agar plate confirmed the presence of Pseudomonas aeruginosa in the patient's pus sample. Examination of the broth dilutions helped determine the right combination of antibiotics for the individual to have. These would be need restorative and own antimicrobial activity resistant to the pathogen, unlike the doctor's prescription of flucloxacillin. Use of a third era cephalosporin with an aminoglycoside should effectively get rid of the problem in the individual following completion of the course of antibiotics.

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