Discuss and analyzed many ways in which digital technologies are fundamentally influencing or changing society. Now, you will take what you have learned and teach others. This assignment has three parts:
First, select one of these topics The impact of the use/growth/spread of digital tools and/or the use of social media (“crowdsourcing” might be an example). The impact of 3-D printers:
(http://www.ted.com/talks/lisa_harouni_a_primer_on_3d_printing.html) The impact of “augmented reality” (Google Glass, iPad apps). The impact of “digital mapping” tools. The impact of “interactive” media such as television or movies. The impact of “wearable computers” (http://www.computerworld.com/slideshow/detaill74332) The impact of robots. (Anybots, for example, or Elder Care Robots). The impact of “telemedicine.” The impact of digital analytics or cloud technologies. The impact of teleconferencing. Second, explain how the digital technology you have chosen will impact the future in one of the following areas: education (elementary, secondary, or post-secondary), law, law enforcement, psychology, business, healthcare, construction, engineering, computer science or any other field in which you have an interest. How will this affect society at large? Example: The use of “augmented reality” in future classrooms at the elementary level and how this will impact society.
Third: Once you have your topic, you will create an online presentation of 8-10 minutes in length which introduces your topic and uses what we know about these tools/trends to extrapolate what impact they will
have on our future.
Possible Tools: You can use whatever is comfortable for you—but an audio component is required. You will need to give a presentation, and it is important that you do not just “read” into the microphone, though having a script and practicing it first will make the job much easier. Pretend that you are standing in front of a crowd—engage them.
Check our Presentation Tools Wiki for ideas. You can also check out: SlideRocket (free if you use your brandman.edu email to sign up—it has a very simple to use audio function) Here’s a page with sample presentations in SlideRocket: http:/Mww.sliderocket.com/gallery/ Powerpoint (If you use Powerpoint, be aware that you will need to use the audio function) Prezi Learning Prezi is easy: http://prezi.com/learn/)
Video (upload it to YouTube, select closed captioning function) Free website template: www.weebly.com (you will need to create an audio file and upload it—this isn’t difficult with Weebly. Post a transcript).
Podcast (with transcript) [there are lots of sites for this, and you can even just create an audio file on your computer and post it on a blog site or a free website, but here’s one choice—sign up for the free plan:
Tuberculosis (TB) is an airborne irresistible malady which is caused by strains of mycobacteria, basically Mycobacterium tuberculosis1. There are around 33% of the total populace are tainted with tuberculosis where nine a huge number of new cases detailed annually2. Despite the fact that tuberculosis can be counteracted and treated, it keeps on causing a huge number of passings each year2. At the point when tainted individual hacks, wheezes or spits, M. tuberculosis is moved into the air and contaminated the individuals who took in the microscopic organisms that existed in beads of saliva3. Basically, tuberculosis will influence the lungs, known as aspiratory tuberculosis3. It will likewise influence different parts of body, for example lymph hubs, bones, cerebrum and kidneys3. Once a man is contaminated with tuberculosis, there are fundamentally three conceivable ways may happen. Initially, the invulnerable framework assumes an imperative job and solid enough to execute the bacteria3. Besides, safe framework isn’t solid enough to fend off the microorganisms yet can manufacture a guarded hindrance against the bacteria3. People who are idly contaminated with M. tuberculosis indicate asymptomatic where these microorganisms lie torpid in the lungs and ready to reactivate after years1. The sickness is regularly reactivated in the individuals who are immunocompromised or by and large debilitated. Ultimately, the resistant framework neglects to eliminate microscopic organisms making the microorganisms develop and spread towards different parts of body which is called dynamic tuberculosis3. In the battle of tuberculosis, World Health Organization (WHO) prescribes widespread Bacille Calmette-Guérin (BCG) inoculation in the nations with high TB burdens4. BCG immunization contains debilitated type of M. tuberculosis which will incite human antibodies to battle against this sort of microscopic organisms. The adequacy of BCG immunization can be extending from 0% to 84%5. This might be because of the recurrence of TB introduction and nature of immunization utilized, prompting contentions on BCG inoculation efficacies4. One of the best contentions is that BCG immunization making positive responses tuberculin skin testing and henceforth meddle with the analysis of inert TB4. Presence of confirmations demonstrating the rates of viability additionally relies upon land area, age at immunization and type of TB additionally confound the circumstance. As of now, TB chemotherapy is comprised of mix of a rundown of first-line drugs isoniazid (INH), rifampicin (RIF), pyrazinamide (PZA) and ethambutol (EMB) 6. In the event that the treatment bombs because of bacterial medication obstruction, or patient unfit to endure, second-line sedates for example para-aminosalicylate (PAS), fluoroquinolones, ethionamide and cycloserine are introduced6. These are considered as second line sedates for the most part either less strong with bigger measurements regimen or more harmful with genuine side effects6. Tuberculosis is by and by treated in two stages, to be specific introductory stage and consistent phase7. In starting stage, the patient will be treated with simultaneous utilization of four first line drugs, with the mean to destroy or control microscopic organisms populace to repeat in quick movement and furthermore dodge the rise of microorganisms resistance7. The treatment decisions accessible for introductory treatment incorporate isoniazid, rifampicin, pyrazinamide and ethambutol7. Streptomycin is utilized once in a while yet can be utilized in patients who tainted with microscopic organisms that are impervious to isoniazid before the treatment is commenced7. The span for introductory stage is 2 months though the constant stage takes 4 months7. Amid the four months of nonstop stage, patients are treated with isoniazid and rifampicin at same doses7. The majority of the TB treatment is managed where tranquilize organization should be completely administered by human services callings since protracted span of treatment causing incompliance in patients7. These patients who are probably not going to be consistence will be given the medications three times each week until the point when the course is finished while patients who ready to conform to the treatment won’t be supervised7. In spite of the chemotherapy treatment and BCG immunization, TB stays as a noteworthy irresistible sickness because of expanding rise of medication safe TB and co-contamination with Human Immunodeficiency Virus (HIV) 6. Since the host barrier in HIV patients is smothered, they are more defenseless to TB diseases. Besides, tranquilize medicate collaborations between antiviral treatment and hostile to TB likewise causing entanglements in treating co-contaminated patients6. Medication safe TB has advanced chiefly in light of ill-advised treatment or incompliance in patients who quit taking their pharmaceuticals previously the microbes is as a rule completely killed since the term of treatment is protracted which takes 6-9 months8, 9. The component included incorporates chromosomal changes in qualities that in charge of medication targets encoding9. At the point when there is a successive aggregation of changes, multi-tranquilize safe tuberculosis (MDR-TB) develops where the M. tuberculosis strains will impervious to two of the most ordinarily utilized medications, Isoniazid and Rifampicin9. Patients with MDR-TB are then depending on the second-line tranquilize classes, fluoroquinolones and the three injectable operators to be specific amikacin, capreomycin, and kanamycin10, 11. The odds to fix would drastically be lessened for patients who tainted with widely sedate safe tuberculosis (XDR-TB), a circumstance where the secluded strains are safe against any of fluoroquinolones and no less than one of three injectable drugs6. With the end goal to battle with the MDR-TB or XDR-TB and streamline the tuberculosis sedate regimen, it is significant to comprehend the system of activity of current utilizing first-line medications and how opposition is produced against these medications. Isoniazid (INH) or isonicotinic corrosive hydrazide is found in 1952, a bactericidal specialist which dynamic against living being of the class Mycobacterium, particularly M. tuberculosis, M. bovis and M. kansassi6, 12. In vivo, INH has appeared to be bactericidal in culture over the initial 48 hours which end up bacteriostatic after this specific time frame12. This demonstrates INH is bacteriostatic for moderate duplicating bacilli yet is bactericidal against quickly isolating mycobacterium. The insignificant tuberculostatic fixation is 0.025 to 0.05ug/ml13. INH is a prodrug that should be actuated by catalaseperoxide hemoporotein, KatG before acts by restraining mycolic corrosive combination and cell divider disturbance in powerless mycobacterium13, 14. This inhibitory activity is just focused to mycobacteria since other microscopic organisms don’t contain mycolic corrosive in the cell wall13. INH acts by hinder enoyl acyl bearer protein (ACP) reductase, InhA, and a beta-ketoacyl-ACP synthase, KasA that are significant in unsaturated fat combination framework for mycolic acid15. Protection from INH is accepted because of changes in quality encoding catalaseperoxidase katG or InhA or lacking KatG 9, 14. Isoniazid is utilized in the liver, basically by acetylation and dehydrazination where moderate acetylator may encounter higher fixation prompts potential poisonous quality before discharged in the pee inside 24 hours13. Rifampicin (RIF), found in 1963, is a lipophilic semisynthetic subsidiary of rifamycin anti-toxin which is created by the maturation of a strain of Amycolatopsis mediterranei6, 9, 16. RIF has bactericidal exercises against a wide range of microorganisms including gram-positive and gram-negative. RIF will restrain the activity of DNA-subordinate RNA polymerase of mycobacteria that is encoded by rpoB through development of a steady medication catalyst complex9. This will stifle the commencement chain development in RNA combination and thus preclude protein blend in M. tuberculosis9. Improvement of protection from RIF is for the most part because of change in 81 base match area of rpoB quality along these lines encourage a direct way to deal with recognize MDR-TB since 85-90% RIF-safe strains are likewise impervious to INH9. RIF produces top plasma centralization of 7ug/mL in 2 to 4 hours after ingestion of 600mg17. It additionally appropriated well to the greater part of the body tissues and liquids, including cerebrospinal liquid since it is lipophilic17. Following retention from the gastrointestinal tract, RIF is disposed of quickly in the bile with less sums discharged through urine17. Pyrazinamde (PZA) is found in 1954 and it produces magnificent sterility impacts against semidormant tubercle bacilli at marginally acidic pH6, 9. The antimicrobial action of PZA is through obstruction with mycolic corrosive union in M. tuberculosis by pyrazinoic corrosive, a functioning moiety of PZA9. Transformation of PZA to pyrazinoic corrosive is intervened by pyrazinamidase protein that is encoded by pncA quality in M. tuberculosis, in this manner demonstrating that these bacilli are delicate to PZA9. Obstruction against PZA advanced when transformation happen at pncA quality that is in charge of pyrazinamidase, consequently influencing the action of this enzyme9. PZA is all around consumed from gastrointestinal tract and is generally disseminated to most tissues and liquid too17. The oral organization of 500 mg PZA produces plasma groupings of 9-12ug/ml following two hours and 7ug/ml after 8 hours17. PZA is processed in liver though the metabolites are discharged through renal glomerular filtration17. Ethambutol (EMB) is found in 1962, goes about as bacteriostatic operator and is dynamic against experiencing cell division6, 18. EMB principally focuses on impedance of cell divider polymerization by represses arabinosy transferase, an imperative catalyst in charge of mycobacteria cell divider biosynthesis9, 18. Since arabinosy transferase chemical is encoded by embC-embA-embB qualities, opposition against EMB advanced is accepted because of transformation of these genes9. EMB is as of now utilized as one of the primary line treatment for tuberculosis for the most part in light of its synergistic impact with other cutting edge medications and its low danger property18. There is approximately 75-80% of an oral dosage of EMB is quickly invested in gastrointestinal tract with retention unaffected when managed with foods19. Furthermore, EMB is conveyed generally to body tissues and liquid, include>