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http://www.jailmedicine.com/
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Cellulitis is a diffuse infection of the soft tissues with no localized area of pus amenable to drainage. The affected area is described as indurated (i.e., warm, red, and swollen). It is also painful. A component of lymphangitis (infection involving the lymphatics) is indicated by red streaking, progressing proximally from the affected area.

An abscess is a localized collection of pus, often with a component of surrounding cellulitis (with the above signs). One sign of an abscess is an area of fluctuance; that is, when you apply gentle digital pressure over the area, you can push and feel a “give,” indicating the presence of fluid underneath. Another sign is that an abscess often seems to “point;” that is, the skin starts to thin from the pressure of the fluid underneath. The distinction between cellullitis and abscess is important. The main treatment for an abscess is incision and drainage (cutting into the abscess and widely opening the abscess cavity). Cellulitis does not warrant this intervention.
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http://practicalplasticsurgery.org/
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http://www.forbes.com/sites/judystone/2015/03/18/choosing-an-antibiotic-for-skin-infections-whats-best/#197415c17065
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Source: http://www.microbiologynutsandbolts.co.uk/the-bug-blog/-how-to-remember-antibiotic-spectrums-of-activity
I am often asked “how can doctors remember the different
antibiotic spectrums of activity”? This is a difficult task as there are so many. Personally I have never found lists of medical information that helpful, I would much rather come up with a mnemonic. However, I’m stumped for a mnemonic to remember antibiotic spectrum of activity, so a list it must be. What I have done though is reduce a very long list into six short related lists, which I hope are easier to remember.

NOT knowing the spectrum of activity of the antibiotic they are prescribing is high up there on the list of situations when doctors make a mistake. NOTknowing leads to patients being given antibiotics which have no activity against the bacteria which are known or suspected to be the cause of an infection. My current pet hate is the use of Teicoplanin to treat UTIs (see Teicoplanin blog...) but I also come across patients being treated for Pseudomonas spp. with Co-amoxiclav which has no activity against Pseudomonas spp., or an anaerobic infection being treated with both Co-amoxiclav AND Metronidazole when either alone would be enough. Sometimes it seems doctors are just guessing or picking their favourites!

Remembering the 6 lists below will help to ensure patients are on an antibiotic that is active against their infection.
  1. Active against Gram-positive and Gram-negative bacteria (Broad-spectrum antibiotics)
  2. Active against anaerobes
  3. Active against Pseudomonas spp.
  4. Active ONLY against Gram-positive bacteria
  5. Active ONLY against Gram-negative bacteria
  6. Active against “non-culturable” bacteria

Lists 1 and 2
Antibiotic Spectrum of Activity Lists 1&2
Click for larger image
Example A: A patient has a perforated appendix. Which antibiotics could be used to cover the mixed bowel flora that will have leaked into the patient’s peritoneum? Any of Co-amoxiclav, Piptazobactam, Ertapenem, Imipenem or Meropenem could be used alone as they are broad spectrum AND cover anaerobes. If Cefuroxime, Ceftriaxone or Cefotaxime were used then Metronidazole would need to be added to cover the anaerobes. You would not use Cefuroxime, Ceftriaxone or Cefotaxime with Clindamycin as this poses too high a risk for Clostridium difficile associated diarrhoea (CDAD).

Example B: In patients with serious penicillin allergies Beta-lactams including Co-amoxiclav, Piptazobactam, Ertapenem, Imipenem or Meropenem are contraindicated. Combinations of antibiotics are therefore needed to cover the gut flora, such as Teicoplanin OR Vancomycin (which only have Gram-positive activity) PLUS Metronidazole (which only covers anaerobes) PLUS either Ciprofloxacin ORGentamicin (both of which have excellent Gran-negative activity).

List 3
Antibiotic Spectrum of Activity List 3
Click for larger image
Example C: A Cystic Fibrosis (CF) patient has an exacerbation of their CF caused by Pseudomonas aeruginosa. What antibiotics would they be treated with? They would be treated with a combination of antibiotics active against Pseudomonas aeruginosasuch as IV Meropenem PLUS IV Tobramycin PLUSnebulised Colistin.
Why a combination of antimicrobials? Combination antimicrobials are used to try and prevent further development of resistance (Pseudomonas aeruginosais notorious for acquiring new resistance mechanisms), in non-CF patients two antimicrobials are usually enough. It is unlikely that bacteria will become resistant to two or more antimicrobials at the same time therefore resistance is less likely to occur. Even if the bacteria do become resistant to
one of the antimicrobials the other agent(s) will be able to kill the bacteria.

List 4 and 5
Antibiotic Spectrum of Activity Lists 4&5
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Example D: A patient has a skin and soft tissue infection but also has a severe allergy to penicillins. Which antibiotics could be used to treat them? Skin and soft tissue infections are almost always caused by Gram-positive bacteria such as Staphylococcus aureus or Beta-haemolytic streptococci therefore Vancomycin, Teicoplanin, Linezolid and Daptomycin would all be capable of treating the infection. It may sound obvious but you cannot use an antimicrobial only active against Gram-negatives to treat a Gram-positive, therefore Ceftazidime, Colistin or Aztreonam would definitely not be appropriate as they do not have any activity against the Gram-positive causes. Broad-spectrum antibiotics would treat the infection but it would be unnecessary as the bacteria are known to be Gram-positive. Broad spectrum antibiotics in this case might lead to unwanted side effects such as CDAD.

List 6
Antibiotic Spectrum of Activity List 6
Click for larger image
Example E: A patient has pneumonia caused by Mycoplasma
pneumoniae
 (a non-culturable bacterium). What antibiotic should they be treated with? Erythromycin, Clarithromycin, Azithromycin, Ciprofloxacin, Levofloxacin and Doxycycline all could be used to treat this patient.

If you can learn these six lists it starts to become much easier to understand why certain antibiotics are chosen to treat certain infections. It also enables you to choose alternatives when patients are allergic to first line antibiotics found in guidelines. Downloada handy postcard of the 6 lists and keep it in your book Microbiology Nuts and Bolts.

Give it a try and see if it helps. Pass it on too. If you can think of any easy way of remembering them then let me know, I’m always keen to know how others have learned their microbiology.
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http://secure.medicalletter.org/JAMA_MRSA
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From: https://firstaidteam.com/2014/01/13/wards-survival-series-everything-you-need-to-know-about-antibiotics-a-3-part-series/

Wards Survival Series: Wards Survival Series & USMLE Study Tips: Choosing Antibiotics

By Michael Spinner
Choosing the right antibiotics to treat an infection can be a daunting task for medical students given the sheer number of different drugs, infections, and organisms we have to memorize. However, a strong understanding of antibiotics is critical as they are some of the most commonly prescribed medications as well as a very common source of questions on boards exams and pimping on the wards. In this post, we offer some useful tips to help guide you as you think about choosing the right antibiotics to treat infections.
When thinking about how to treat an infection, first consider the likely causative organism. Is the organism likely bacterial, viral, fungal, or parasitic? Remember that antibiotics are only indicated to treat bacterial infections (with a few exceptions like metronidazole which also has excellent anti-protozoal coverage). The vast majority of upper respiratory infections and some lower respiratory infections (e.g. acute bronchitis) are caused by viruses and thus do not require treatment with antibiotics. Remembering this simple fact will help you to avoid exposing patients to unnecessary side effects and prevent antibiotic resistance.
In the case of a likely bacterial infection, first consider which of the following broad groups of bacteria are the most likely culprits: gram-positives, gram-negatives, anaerobes, and/or atypicals. For community-acquired pneumonia, the most common causative organisms are gram-positive (e.g. Streptococcus pneumoniae) or atypical bugs like MycoplasmaChlamydia, and Legionella. Thus, an appropriate antibiotic would cover both gram-positive and atypical organisms, making azithromycin an excellent choice. For appendicitis or diverticulitis, you should cover empirically for colonic anaerobes and gram-negative enterics, making piperacillin/tazobactam an appropriate agent.
Grouping bacteria into these four broad groups is a great place to start when thinking about antibiotic coverage. However, memorizing the specific antibiotics that cover certain bugs (especially MRSA and Pseudomonasaeruginosa) can be high-yield for board exams and on the wards. A list of the antibiotics that cover MRSA and Pseudomonas is provided below:
MRSA coverage                     Pseudomonas coverage
Vancomycin                           Piperacillin/tazobactam
Clindamycin                           Cefepime, ceftazidime
Doxycycline                           Carbapenems (except ertapenem)
TMP/SMX                              Aztreonam
Linezolid                                Aminoglycosides
Daptomycin                           Fluoroquinolones
In addition to considering the likely causative organism, also consider the source of infection. If the antibiotic does not adequately reach the source then its coverage won’t matter! For example, both doxycycline and vancomycin cover MRSA, but the preferred treatment depends on the source. Oral doxycycline is a reasonable choice to treat MRSA cellulitis but would not be an appropriate choice for MRSA bacteremia or osteomyelitis. A bloodstream MRSA infection would require treatment with an intravenous agent like vancomycin. Similarly, treating meningitis requires an agent with good CSF penetration like ceftriaxone.
Last, be sure to consider the side effects. Aminoglycosides and vancomycin are nephrotoxic and should be avoided in renal failure. Numerous antibiotics have adverse effects in utero and should be avoided in pregnancy. Penicillin and sulfa allergies are extremely common and will often affect antibiotic choices.
As with reading a chest X-ray or EKG, having a systematic approach to choosing antibiotics will help you to approach this topic with confidence on the wards and board exams. Whether you’re studying for Step1 or Step 2 or just trying to survive on the wards, I hope that these pointers will serve you well!
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source: http://womeninbalance.org/resources-research/bioidentical-progesterone-vs-synthetic-progestins/

Confusion exists, even among leading experts in the field of hormone research, between the terms progesterone, progestin, and progestogen. Although these terms are often used interchangeably, they are not synonymous.
Until an authoritative definition is formally adopted, the following reflects the current culture of the usage of these terms, and clarifies how they are used by Women in Balance: “progesterone” refers to the hormone produced in the body, or produced from a plant source but still chemically and structurally identical to human progesterone, and it is therefore referred to as “bioidentical” or “natural”.
In contrast, “progestin” refers to a hormone that is synthetically produced and differs in structure from progesterone. There are numerous synthetic progestins used in hormone therapy, in contrast to only one molecule referred to as progesterone. “Progestogen” (sometimes spelled “progestagen”) is a general term for hormones that act like progesterone in the uterus, and therefore includes both progesterone and progestins.
There is increasing evidence that, by virtue of their different chemical structures, synthetic progestins do not always act as progesterone would at the same target tissues. This has long been understood with respect to treatment of pregnancy and fertility issues, when progesterone is effectively prescribed, yet synthetic progestins are contraindicated.
While synthetic progestins may mimic some of progesterone’s effects, progestins may react differently with progesterone receptors in the body. A significant consequence of the side effects seen with synthetic progestins has been an increase in the risk of developing breast cancer. Clinical trials such as the Women’s Health Initiative, in which more breast cancer was seen in the group taking progestins, did not study natural progesterone
STD
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https://www.atsu.edu/faculty/chamberlain/website/lectures/lecture/stdd.htm