#benzylpenicillin
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Etest
“Etest being used to determine the susceptibility of Neisseria gonorrhoeae to benzylpenicillin.” - via Wikipedia
#the commons page didn’t have a description so i pulled this one from the article itself. seemed best to put a caption on this one.#wikipedia#wikipedia pictures#wikimedia commons#medicine#medicalcore#medcore#medicore#medical aesthetic#labcore#stemcore#laboratory aesthetic#science#antibiotic resistance#antimicrobial resistance#bacteria#microbiology#Neisseria gonorrhoeae#N. gonorrhoeae#neisseria#infectious diseases#etest#Epsilometer test#antibiotic sensitivity test#antimicrobial sensitivity#benzylpenicillin#penicillin g#peng#benpen#antibiotics
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Oropharyngeal primary syphilis by Dr Louis Noël in Journal of Clinical Case Reports Medical Images and Health Sciences
A 48-years-old healthy male was referred to our tertiary care center from an otorhinolaryngologist. The patient complained of odynophagia for the last 4 months, without any history of smoking nor chronic alcohol intake. A biopsy was performed and diagnosed chronic inflammation with fungal mycelia. Oral fluconazole did not bring any improvement.
Upon arrival, the examination shows some granular and erythematous pharyngeal lesions (Figure 1). A diagnostic work-up with local biopsies and serologies was done.
The PCR came back positive for Treponema pallidum (negative for herpes virus, chlamydia, and gonorrhea). Syphilis serologies were also positives (VDRL titer, 1:8; TPHA titer 20’480). The patient received one intra-muscular benzathine benzylpenicillin injection (2.4 million I.U.). The odynophagia and the lesions disappeared within 48 hours (Figure 2), without relapse for over two years.
Syphilis should be considered in every acute and chronic pharyngeal lesion, as oral sex may not be disclosed upon first medical consultation.
We declare no conflict of interest nor funding source. We obtained the patient’s written consent for the publication of this case report.
#Oropharyngeal primary syphilis#odynophagia#Oral fluconazole#jcrmhs#Journal of Clinical Case Reports Medical Images and Health Sciences submissions#Clinical decision making#Clinical Images journal
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Listeria
For whatever reason it reminds me of Desperate Housewives and Wisteria lane. Or just Wisteria in general.
It's unfortunately it's anything but wistful or romantic.
This is inspired by the netflix series Poisoned. I hate that title but it's a great watch. I learned a lot from it. I highly recommend it particularly for medical students and residents etc.
So, listeria are gram positive rods (most bacilli are negative) making this relatively easier to remember (purple rods). Also catalase positive. IT's also a facultative anaerobe - so both cultures may be positive (aerobic and anaerobic bottles).
the species that is the culprit for major human pathogens is Listeria monocytogenes.
At increased risk groups (more likely to die of Listeriosis) - the immunocompromised and extremes of life, including the elderly, pregnant women and neonates. Immunocompromised: HIV, anyone on long term highish doses of steroids, leukaemia/oncology patients etc. Worryingly, incubation time is 3-90 days in these groups, so it's difficult to really trace or keep track of. Pregnant women are at 20x higher risk of acquiring the severe form.
Source: CDC
Hence why during pregnancy you're advised not to consume raw salads, fruits, cold cuts, soft cheeses, sprouts and smoked salmon or sushi, no mayo and no raw egg (definitely no raw milk) etc. Similarly, common recommendation is you serve none of these to children under the age of 1. It naturally lives in soil (hence avoidance of raw sprouts) and can live in animals. So it can frequently contaminate food.
Image Source: SA Health
As with COVID (I can't believe I'm using COVID as a measure of things), it can cause mild food borne illness (nausea, vomiting diarrhoea, myalgias, even fevers) to invasive disease causing sepsis and even meningitis or encephalitis. Incubation time is a few days in the mild form.
IMage source:
Death by Listeria when you have the severe form (Listeriosis) is 20%, astonishingly high given you have a 1% chance of dying from Salmonella.
It's a small risk but the issue is that complications and fatality if you do acquire is high. It's also highly preventable, but the challenge is food safety and avoiding certain foods as a consumer.
i.e. in pregnancy, most will have diarrhoeal illness that's mild. But in the subset that get invasive disease and really unwell, there's a 20% risk of miscarriage, risk of premature labour and risk of still birth at 3% in the US. In the states, pregnant women are also 10x more likely to get Listeria infection. That is, illness after exposure.
On the final note of prevention, also always properly refridgerate food to 4 degrees celsius and cook meat to 165 fahrenheit or 73 degrees celsius. As I've learned from the Poisoned documentary, you can ask restaurants to do this, ask them to use an internal thermometer to measure - as rare/medium rare etc have no meaning as it pertains to food safety. If they can't, order something else.
With meningoencephalitis, we just presume that Listeria is a possibility and treat empirically while awaiting investigations.
Investigations: - CSF (lumbar puncture) in event of signs of meningism or encephalitis (classic headache/fever/stiff neck/rash and/or acute confusion or seizure AND fevers) --> expect the classic features of bacterial meningiits and gram stain positive for purple rods - PCR - stool cultures have no value - blood cultures--> look for gram positive rods in the preliminary findings, expect a call from the lab Empirical therapy: - none in asymptomatic or mild disease. just monitoring until symptoms resolve and supportive care (fluids etc.) - Listeria is a notifiable disease to the health department in most Western countries that keep track of outbreaks. - in the US, standard treatment is ampicillin. - in Australia at least, standard therapy is IV benzylpenicillin, 2.4 g 4 hrly in meningitis or encephalitis and everyone is just started on this until bug identification/gram staining and sensitivities return. - in hypersensitivity, bactrim is used. - cephalosporins have no activity against them (or "inherently resistant), hence you can see IV ceftriaxone and benzylpen in the drug regimen for empirical therapy of meningitis - cef covers gram negatives, strep pneumo (most common cause of meningitis) and neisseria meningitidis - duration of therapy in severe disease: 3 weeks, 6 weeks if immunosuppressed
Really great summary here.
Random historical trivia
listeria is named for Dr. Joseph Lister, a British surgeon who introduced sterilisation of equipment and antiseptics to surgery, improve post op care and observed that microbes are the cause of cases of poor wound healing or post op infections. he also began to look at them under the microscope as an early pioneer of bacteriology.
Lister's father by the way, made compound microscopes for a living, so lister became proficient at using this and started publishing articles during medical school
this also led to a lot more research on inflammation and coagulation
weirder trivia: in his med school days, surgeons commonly did not wash hands between patients and some didn't even change gowns, glorifying how busy they where by how many stains were on it by the end of the day
so unsurprisingly his early battles to pioneer antiseptics and aseptic techqniues to prevent the transmission of infection in surgical patients were pretty uphill
Resources CDC guidelines WHO guidelines FDA Statpearls --> great at covering basic physiology and pathology etc. in a short form. Australian therapeutic guidelines - unfortunately not free.. so won't bother to link. If you work at any large-ish Australian hospital you'll have 'free' access. Wikipaedia US list of outbreaks CDC recommendations on foods to avoid vs okay to eat to avoid Listeria
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Alexander Fleming was born on August 6, 1881. A Scottish physician and microbiologist, best known for discovering the world's first broadly effective antibiotic substance, which he named penicillin. His discovery in 1928 of what was later named benzylpenicillin (or penicillin G) from the mold Penicillium rubens is described as the "single greatest victory ever achieved over disease". For this discovery, he shared the Nobel Prize in Physiology or Medicine in 1945 with Howard Florey and Ernst Boris Chain. Fleming was knighted for his scientific achievements in 1944. In 1999, he was named in Time magazine's list of the 100 Most Important People of the 20th century.
#alexander fleming#antibiotics#penicilln#medicine#nobel prize#nobel prize winners#science#science history#science birthdays#on this day#on this day in science history
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Funguary 2024 Day 7
☁️ Week 1: Celestial 🧽 Penicillin
This guy is a future doctor, and he is currently investigating the cause of mold and green spots on his body. Maybe he can use it in medicine.
I indicated benzylpenicillin by mistake, but I think it's no big deal.
Other arts:
🧢 Mycena Subcyanocephala
🪸 Lilac Coral Fungus
🦃 Turkey Tail
☁️ Cystolepiota
🏮 Filoboletus Manipularis
🪽 Angel Wings
🧽 Penicillin 🍄
👹 Satan's Bolete
🌳 Silver Leaf Fungus
🗡️ Destroying Angel
🪺 Birds Nest Fungus
🧟 Dead Man's Fingers
👒 Lilac Bonnet
🩸 Bleeding Tooth
🪮 Black Velvet
🍜 Enoki
🍘 Dotted Stem Bolete
🌧️ Inky Cap
☕ Black Trumpet
🧤 Amethyst Deceiver
🍚 Puffball
💧 Dewdrop Bonnet
🫂 Mycorrhizal Network
🎭 False Blusher
🐕 Stinkhorn
🌵 Prototaxites
🪬 Blue Coprinopsis
🐝 Icing Sugar Fingus
💋 Magic Mushroom
Organizer: @/feefal
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What Is Antibiotic Resistance and Why Is It Important?
Antibiotic resistance is also known as antimicrobial resistance (AMR) and represents one of the biggest threats to public health and development in the world. Bacterial AMR was responsible for an estimated 1.27 million deaths globally in 2019 and contributed to a further 4.95 million deaths.
The main drivers behind the development of drug-resistant pathogens are the overuse and misuse of antimicrobials in plants, animals, and humans.
What Are Antimicrobial Resistant Bacteria?
Antimicrobial resistant bacteria are bacteria that aren’t killed or controlled by antibiotics. They can both survive and multiply even when an antibiotic is present. While many types of bacteria that cause infections can gain resistance to some antibiotics, bacteria that’s resistant to many antibiotics are termed multi-resistant organisms (MROs). Furthermore, some types of bacteria have a natural resistance to antibiotics; for example, benzylpenicillin has little effect on most bacteria present in the human gut.
The Devastating Effects of AMR
AMR is responsible for a huge global death toll, and one that is likely to increase unless action is taken. While inequality and poverty exacerbate its consequences and effects, AMR impacts all countries, although middle and low-income nations are most affected. As well as making it harder to treat infections, it makes undertaking many other treatments significantly riskier.
As well as the devastation of disability and death, AMR comes with a huge economic cost, with the World Bank estimating that it could result in around $1 trillion to $3.4 trillion worth of GDP losses per year by 2030 and $1 trillion in additional healthcare costs by 2050.
youtube
How Can the AMR Challenge be Tackled?
Those with experience in this field – such as Alec Simonson, who was involved in bioinformatics and neuropharmacological research during his studies – know that one of the most important ways to prevent AMR is to use antibiotics properly. This means reducing the overprescribing of antibiotics and preventing unnecessary use. It’s also important that patients complete the entire course of any antibiotics they are prescribed so the medication will be fully effective and not promote resistance. Good hygiene (such as handwashing) and the deployment of appropriate infection control procedures will also play a key role in tackling AMR.
The Global Action Plan (GAP) on AMR was adopted by countries during the 2015 World Health Assembly. Adoptees committed to developing and implementing multisectoral national action plans to tackle AMR, using a One Health approach.
For information about World AMR Awareness Week, take a look at the embedded PDF.
#Alec Simonson#AMR#Antibiotic Resistance#world health organization#who#healthcare#health and medicine#bacteria#effects of amr#Antimicrobial Resistant Bacteria#Youtube
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Isaac took the time to read her questions carefully. Once he was done, he opened her file, offering her a polite smile. He was not planning on lying to her, not about that at least. "It might not make a lot of sense to you, but I can tell you what we found in your blood. We found traces of Ciprofloxacin, Benzylpenicillin and Tetracycline. Those are antibiotics, and can actually make you ill when taken that way."
"We also found traces of alprazolam and diazepam, strong anxiolytics that were meant to keep you sedated. Now, If there is something you don't understand, you can tell me."
⋆ ˚。⋆୨୧˚ she follows him back to the desk , taking a seat across from him like she had done the first day she got here. it had the same chill to it as she felt then , but that could be the whole of the hospital , and it could also be from how tired she was that she could not get warm. she didn’t pay it much mind , she just let it be. when he assures her she can ask about his own well being , she smiles. “ o —- okay , t —thank y — you. “ she is aware he has to be more invested in her well being since this is a hospital , but she could not help but ask. she clasps her hands , settling them in her lap , waiting his response. ⋆ ˚。⋆୨୧˚
#he's not sugar coating it lol#&(valerie)#isaac (oh now you want to talk to god?)#read at your own discretion#drugging tw#dcmur3
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Discovery Of Penicillin
penicillin, perhaps the earliest despite everything quite possibly of the most generally utilized anti-toxin specialist, got from the Penicillium form. In 1928 Scottish bacteriologist Alexander Fleming originally saw that states of the bacterium Staphylococcus aureus neglected to fill in those region of a culture that had been coincidentally tainted by the green form Penicillium notatum. He secluded the form, developed it in a liquid medium, and found that it created a substance fit for killing a large number of the normal microbes that taint people. Australian pathologist Howard Florey and English natural chemist Ernst Boris Chain separated and cleansed penicillin in the last part of the 1930s, and by 1941 an injectable type of the medication was accessible for helpful use.
Discovery Of Penicillin
Have some familiarity with penicillin's revelation by Alexander Fleming and advancement by Ernst Chain and Howard Florey and its outcome in treating the injured in The Second Great War Have some familiarity with penicillin's revelation by Alexander Fleming and advancement by Ernst Chain and Howard Florey and its outcome in treating the injured in Universal Conflict IISee all recordings for this article The few sorts of penicillin blended by different types of the shape Penicillium might be separated into two classes: the normally happening penicillins (those framed during the course of form maturation) and the semisynthetic penicillins (those wherein the construction of a compound substance — 6-aminopenicillanic corrosive — found in all penicillins is changed in different ways). Since it is feasible to change the qualities of the anti-microbial, various kinds of penicillin are delivered for various helpful purposes.
The normally happening penicillins, penicillin G (benzylpenicillin) and penicillin V (phenoxymethylpenicillin), are as yet utilized clinically. In light of its unfortunate security in corrosive, quite a bit of penicillin G is separated as it goes through the stomach; because of this trademark, it should be given by intramuscular infusion, which restricts its value. Penicillin V, then again, commonly is given orally; it is more impervious to stomach related acids than penicillin G. A portion of the semisynthetic penicillins are likewise more corrosive stable and consequently might be given as oral prescription.
All penicillins work similarly — specifically, by restraining the bacterial catalysts answerable for cell wall amalgamation in recreating microorganisms and by enacting different proteins to separate the defensive mass of the microorganism. Thus, they are viable just against microorganisms that are effectively imitating and delivering cell walls; they likewise hence don't hurt human cells (which essentially need cell walls).
A few kinds of beforehand defenseless microbes, like Staphylococcus, have fostered a particular protection from the normally happening penicillins; these microorganisms either produce β-lactamase (penicillinase), a chemical that upsets the inner construction of penicillin and in this manner obliterates the antimicrobial activity of the medication, or they need cell wall receptors for penicillin, extraordinarily lessening the capacity of the medication to enter bacterial cells. This has prompted the development of the penicillinase-safe penicillins (second-age penicillins). While ready to oppose the action of β-lactamase, be that as it may, these specialists are not as successful against Staphylococcus as the regular penicillins, and they are related with an expanded gamble for liver harmfulness. Besides, a few types of Staphylococcus have become impervious to penicillinase-safe penicillins; a model is methicillin-safe Staphylococcus aureus (MRSA).
extreme touchiness to penicillin extreme touchiness to penicillin Penicillins are utilized in the treatment of throat contaminations, meningitis, syphilis, and different diseases. The central symptoms of penicillin are touchiness responses, including skin rash, hives, enlarging, and hypersensitivity, or unfavorably susceptible shock. The more serious responses are phenomenal. Milder side effects might be treated with corticosteroids yet typically are forestalled by changing to elective anti-toxins. Anaphylactic shock, which can happen in recently sharpened people inside the space of seconds or minutes, may require quick organization of epinephrine.
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makes me laugh every time i hear a doctor call benzylpenicillin benpen
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#BENZYLPENICILLIN = #PENICILLIN G injectable
Powder for injection in vials of:
1 MIU (600 mg), to be dissolved in 2 ml of water for injection or 0.9% sodium chloride
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5 MIU (3 g), to be dissolved in 5 ml of water for injection or 0.9% sodium chloride
For IM injection or slow IV injection through an infusion tube (3 to 5 minutes) or infusion (60 minutes) in 0.9% sodium chloride or 5% glucose.
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Dosage: Severe leptospirosis
Child: 50 000 IU (30 mg)/kg (max. 2 MIU or 1200 mg) by IV injection every 6 hours
Adult: 1 to 2 MIU (600 to 1200 mg) by IV injection every 6 hours
Neurosyphilis
Adult: 2 to 4 MIU (1200 to 2400 mg) by IV injection every 4 hours
Congenital syphilis
50 000 IU (30 mg)/kg by IV injection every 12 hours from D1 to D7, then
50 000 IU (30 mg)/kg by IV injection every 8 hours from D8 to D10
Duration: Severe leptospirosis: 7 days
Neurosyphilis: 14 days
Congenital syphilis: 10 days
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Remarks: Do not confuse short-acting benzylpenicillin, administered several times a day by IV route, with long-acting #penicillins (#benzathine benzylpenicillin and #procaine benzylpenicillin) administered by IM route only.
Do not mix with other drugs in the same syringe or infusion.
Storage:– – Below 25 °C
Once reconstituted, suspension must be used immediately.
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Syphilis!
Syphilis is caused by Treponema pallidum. This is a spirochaete, with a low reflective index, and it is motile using its spiral shape to propel itself (it has internal flagella attached to the cytoplasmic membrane). It is too thin to visualise with gram staining, but it can be viewed using dark-field, electron, Steiner silver stain and fase-contrast methods.
Treponema palladium can also cause Yaws (burrows under the skin), Pinta (hyperkeratosis) and Bejel (much more like syphilis, but not an STI; spread using same cooking utensils).
There are 3 stages of syphilis:
Primary: Chancre: immune response causes tissue degradation without pain, which eventually disappears.
Secondary: 6-8 weeks after infection, patients present with generalised malaise and rashes, even palmar rashes. This is systemic.
Tertiary: after 3-30 years of a latent period, symptoms can reappear, including gummas across body/tongue (do not contain many bacteria cells, mainly an immune response), cardiovascular/meningovascular lesions (leading to aneurisms/strokes), and ‘general paresis of the insane’, aka neurosyphilis (hypersensitivity in the brain).
Lesions from syphilis often allow secondary infections to occur, such as S. aureus.
Spread:
Syphilis spreads HORIZONTALLY as an STI or via contaminated blood. It spreads VERTICALLY as congenital syphilis.
Congenital syphilis is typified with Hutchinson’s teeth, Sabre teeth, bone lesions and neurosyphilis; however it can present anywhere between 5-25 years old. The mother should be treated prophylactically if there is a risk.
Diagnosis:
Using exudate/biopsy from chancre.
Using serology to identify reagin, an antibody produced during body damage, using VDRL/RPR testing. FTA serology finds antibodies specific to T. pallidum. These tests rely on antigen and antibody complexes binding to an anti-human antibody which is conjugated to a fluorophor at the FAB region for visualisation.
It is found highest between the ages of 20-40, and is higher in men: 9:1. It mostly affects men who have sex with men. Education around HIV and AIDS also decreased the incidence.
Treatment:
Benzylpenicillin or a macrolide (bacteriostatic, such as the new azithromycin) are used to block the peptide exit tunnel of T. pallidum’s 50S ribosomal subunit.
Old treatments: Mercury, salvarsan, malaria (increases temperature beyond limits of the bacteria), and penicillin.
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Hemophilus ducreyi causes painful ulcers.
Haemophilus ducreyi is a fastidious gram-negative coccobacillus bacteria. It causes the sexually transmitted disease chancroid, a major cause of genital ulceration in developing countries characterized by painful sores on the genitalia. Chancroid starts as an erythematous papular lesion that breaks down into a painful bleeding ulcer with a necrotic base and ragged edge. More recently, it has also been found to cause chronic skin ulceration away from the genitalia, infect children and adults, and behave in a manner that mimics yaws.
H. ducreyi can be cultured on chocolate agar. It is best treated with a macrolide, e.g. azithromycin, and a third-generation cephalosporin, e.g. ceftriaxone. H. ducreyi gram stain resembles a "school of fish."
Treponema pallidum = syphilis. Tx is 2.4 million units PCN G benzathine IM x1.
Early infections
The first-line treatment for uncomplicated syphilis (primary or secondary stages) remains a single dose of intramuscular benzathine benzylpenicillin. Doxycycline and tetracycline are alternative choices for those allergic to penicillin; due to the risk of birth defects, these are not recommended for pregnant women. Resistance to macrolides, rifampicin, and clindamycin is often present. Ceftriaxone, a third-generation cephalosporin antibiotic, may be as effective as penicillin-based treatment. It is recommended that a treated person avoid sex until the sores are healed.
Late infections
For neurosyphilis, due to the poor penetration of benzathine penicillin into the central nervous system, those affected are given large doses of intravenous penicillin G for a minimum of 10 days. If a person is allergic to penicillin, ceftriaxone may be used or penicillin desensitization attempted. Other late presentations may be treated with once-weekly intramuscular benzathine penicillin for three weeks. Treatment at this stage solely limits further progression of the disease and has a limited effect on damage which has already occurred. Serologic cure can be measured when the non-treponemal titers decline by a factor of 4 or more in 6–12 months in early syphilis or 12–24 months in late syphilis.
I have to read about syphilis because it has so many stages and I don't remember everything.
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WIP DAY!!
Also tagged by @confidentandgood for this one, thank you!! As you all may know I'm working on several new projects with Juliette's new verses (Flatliners, the Lost Boys, and Stand By Me thanks to my resurfacing obsession with Kiefer Sutherland) but honestly I have nothing substantial written for those verses 😅 sooo here's some classic Jord and Orca from the ongoing fic "Someday." TW for a bit of medical talk but not anything graphic.
"What were his vitals when you first found him?" Asked the medic examining Orca.
"Pulse is strong and bounding, about 125 last I took it. BP 130/86. O2 sat 97%. Labored breathing. GCS score of 14, I'd say. Started him with a bolus of hypertonic saline, the site was on his left arm so I'd use the right when you stick him."
The recording medic nodded. As the examining one continued to check Orca over, the third inserted an IV drip of benzylpenicillin, morphine, and human anti-tetanus immunoglobulin into his unaffected forearm, and then placed an oxygen mask over Orca's face. He took Orca's glasses and went to toss them, but Orca grabbed his hand.
"Oi! Don't throw those out, china, I wanna keep 'em! Jord, take the glasses from him!" Orca yelled.
Jordanna held out her unhurt hand. "You heard the man. Give them here."
The medic shrugged and handed Jordanna the glasses, and she put them away in her jump bag. The helicopter finally took off, so Jordanna sat back in one of the seats.
"You doin' alright, love?" She asked Orca, smiling at him. He looked oddly at peace, probably from the morphine kicking in.
"Just fine," he replied in a lazy tone, his eyelids struggling to stay open. "This is the good shit."
Jordanna giggled. "Yeah, it sure is."
One of the medics came over to Jordanna, sitting beside her, uncomfortably close. She slid away a bit.
"Lieutenant Lewis, are you injured?" The medic asked.
She shrugged. "Left hand's probably broken, a couple of ribs are hurt. I'm okay though, don't start a report for me. Don't take my vitals or anything."
The medic raised an eyebrow. "Ma'am, if you're hurt, we need to open a case. Can I check your hand?"
Jordanna jerked her hand away from him. "No. And don't open a case for me, or I'm gonna kick you off what still remains of the squad. You do know I'm head of medicine for Shoreline, don't you?"
His eyes widened and he backed away. "Oh, you're THAT Lieutenant Lewis? Jordanna Lewis? My apologies, ma'am. We'll keep our attention on the commander."
"I thought so," Jordanna said under her breath as the medic got up and returned to the other side of the helicopter.
"Hey, Jord?" Orca called to her, still in a sleepy daze.
Jordanna leaned towards him. "Yeah?"
"Will you sing for me?" He asked. "Just one song?"
She rubbed the back of her head and felt her cheeks warm up. "Oh, Orca...not in front of these guys…"
"Please?"
With one look at him, at how helpless he looked in that state, Jordanna changed her mind. She leaned back against the seat and smiled.
"On a cobweb, afternoon,
In a room full of emptiness,
By a freeway, I confess,
I was lost in the pages,
Of a book, full of death,
Reading how we'll die alone,
And if we're good, we'll lay to rest,
Anywhere we want to go.
In your house, I long to be,
Room by room, patiently,
I'll wait for you there,
Like a stone,
I'll wait for you there,
Alone…
Alone…"
As Jordanna sang the last of the chorus, she leaned her head back against the wall and closed her eyes, finally allowing herself to rest. She knew Orca was resting, too, as he'd gone quiet and wasn't chatting the medics' ears off. It wasn't sleep, but the small amount of shuteye that Jordanna got on the ride to the hospital was enough to distract her from the pain.
#wip day#tag game#my ocs#my writing#jordanna lewis#orca#uncharted oc#orca uncharted#x: those cunts from shoreline
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I got 25% of my questions correct today so who's the winner in all of this? The people I paid for their question bank, probably
100 days of productivity
Day 10
RS/CVS
endocarditis prognosis: viridans = good prognosis (overall strep mortality ~5%); staph/culture-negative = poor prognosis (overall staph mortality ~30%); prosthetic valves and low serum complement also assoc. w/ poor prognosis
prosthetic valves = gent + RIF + fluclox if known MSSA source + vanc if unknown MSSA or suspected MRSA or PCN allergy
native valves = fluclox if MSSA; benzylpenicillin if strep + low-dose gent if less PCN-sensitive; vanc + RIF if PCN-allergy or MRSA; amox/(vanc if PCN-allergic) + low-dose gent if neither
latent TB in HIV → INH x9 mos
AV block: MILD RASH: myotonic muscular dystrophy, IHD, Lyme, digitoxicity (often +atrial tachy), RHD, aortic abscess/aortic root dilation, sarcoid, hypo/hyperkalaemia
CNS
NCS: ↓compound muscle action potential amplitude → axonal neuropathy
NCS: reduced velocity/conduction blocks → myelin disorders; reduced amplitude → axonal disorders
dizziness + absent corneal reflex = acoustic schwannoma
mumps meningitis causes low CSF glucose! however, other CSF stigmata point to viral disease (normal to mildly elevated protein, lymphocytes, negative stains/cultures) (differentiate from TB by acuity of mumps vs subacuity/chronicity of TB + cobwebbing in TB + *markedly* elevated protein in TB; PCR is 75% sensitive for TB)
GIT
best single-marker indicator of severity in acute pancreatitis is CRP; good predictor of necrosis
mucoid diarrhoea + very mild anaemia + hypokalaemia → villous adenoma (IRL, anaemia → r/o ca colon; but a colonoscopy will catch the adenoma anyway)
inducing Crohn's remission: 1. glucocorticoids + salazines 2. add-on azathioprine/6-mercaptopurine or MTX if cannot use aza/6-MP 3. add-on infliximab (I am unsure why aza/6-MP are used for inducing remission as they take upwards of 2-3 months to take effect; they are generally excellent for *maintaining* remission, not inducing it, but them's the guidelines I guess)
Endo/Repro/Infections
9am cortisol between 100-500 → inconclusive; proceed to cosyntropin test (but as long as levels <500 you will proceed with cosyntropin stimulation test)
urethritis NAAT-neg for gono/chlam → doxy x1 wk or azithromycin (NAAT will only be positive 2 weeks after likely transmission event)
malaria: sensitivity of QBC is greater than than of thick smear for parasite burden estimation, but less than that of thin smear for species identification
Onc/Haem
AIHA: in warm, the haemolysis occurs *extravascularly* (hence haptoglobin and peripheral smear will NOT show stigmata of haemolysis); in cold, the haemolysis occurs *intravascularly* (so hapto/smear WILL reflect haemolysis)
myelofibrosis = V617F JAK2 mutation (asso. w/ teardrop poikilocytosis)
Renal/Biochem/Toxo
MDRD equation for eGFR: CAGE: Creat, Age, Gender, Ethnicity
ADPKD assoc. w/ AR (aortic root dilation), MVP/MR, TR
warfarin × azathioprine interaction → ↓warfarin effect → impaired thromboprophylaxis in immunosuppressed (mechanism unknown)
atorvastatin (only) × digoxin → digitoxicity (inhibition of digoxin transport by the p-glycoprotein efflux transporter)
all statins interact with fibrates, but fenofibrate has the least potential for precipitating the myotoxic interaction and should be preferred when both statins and fibrates must be prescribed
thiazides cause impotence in up to 33% of patients???
if VICKO STUMBLED, luckily for him those toxins are dialysable: Valproate, Isoniazid/Isopropyl alcohol, Carbamazepine, Kerosene/Ketones, Organophosphates, Salicylates, Topiramate, Urea, Methanol/Methylxanthines (caffeine, theophylline etc), Barbiturates/Benzos, Lithium, Ethylene glycol/Ethanol, Dabigatran
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