Showing posts with label CAP14. Show all posts
Showing posts with label CAP14. Show all posts

Wednesday, 22 November 2017

Meningitis

Causes
Viral or aseptic meningitis is the most common form and may be caused by enteroviruses.
Meningococcal disease is the most common (Neisseria meningitides) - infancy and adolescence and over the Winter months.
Pneumococcal - commonest cause in elderly people. Often have a distant focus of pneumococcal infection like pneumonia, otitis media, mastoiditis, sinusitis or endocarditis. Has a 30% mortality rate.
TB meningitis - often develop gradually over days or even weeks and is more  common in the immunocompromised, especially with HIV.
Listeria meningitis remains uncommon. Neonates, the elderly, and immunocompromised people are at greatest risk.


Recurrent lymphocytic meningitis, also known as Mollaret’s meningitis, is a rare disease that is estimated to have a prevalence of 2.7 per 100 000 population. HSV-2 is the most common cause of recurrent lymphocytic meningitis, being responsible for 84% of recurrent meningitis in one study.
A suddenly worsening headache, followed by emerging signs of meningism, is often associated with rupture of the abscess. Rupture of a brain abscess is associated with a high mortality: up to 80%. Emergency surgery is indicated.


Clinical Presentation When a patient recovers from bacterial meningitis, headache, fatigue, and difficulty with coordination, concentration, and memory may persist for several months.


Rash - may be petechial, or in its early stages may be erythematous. The rash occurs in at least 60% of adults.


Triad of fever, headache, and neck stiffness(70% sensitivity) in less than 50% of patients. Changes in mental state are relatively sensitive and tend to occur more often in bacterial than viral meningitis.

Kernig's test is positive if there is pain or resistance in the lower back or posterior thigh when the knee is extended while the hip is flexed to 90°. Kernig's sign can be a useful test if positive, but a negative test does not exclude meningitis.

Brudzinski’s sign is not specific for meningococcal meningitis. You can elicit the sign by passive flexion of the neck, resulting in flexion of the hips and knees if positive.


Encephalitis  has a similar presentation to meningitis, but confusion and drowsiness tend to be more prominent.


Management of Suspected Meningitis in the Emergency Department
  1. Recognise
  2. Investigate – Take extra two EDTA (purple) tubes for meningococcal or pneumococcal DNA using PCR. Do not wait for the results before commencing treatment. It is difficult to differentiate viral meningitis from bacterial meningitis on clinical grounds alone so we need to do a LP.
  3. Treat –
    a. Sepsis 6 with antibiotics as per trust antimicrobial guidelines
    (Ceftriaxone 2g + amoxicillin 2g if >50years or immunocompromised)
    b. Dexamethasone 10mg IV
    c. Aciclovir if features of encephalitis (fluctuating consciousness, motor or sensory deficits, altered behaviour and personality changes, and speech or movement disorders).
    There are currently no treatments with a proven benefit for the common causes of viral meningitis, although acyclovir is often used, despite it being nephrotoxic and lowering seizure threshold. It does reduce the mortality of encephalitis from 70% to less than 30%. Treatment should be supportive.
  4. CT would be indicated if there are focal neurological signs, papilloedema, controlled or uncontrolled seizures, GCS <12 or diagnostic uncertainty. The medical team may ask the ED team to arrange the CT, but this should not delay their review of the patient.
  5. For continuity of care, it is expected that the medical team will report “acute meningitis” to  Health Protection Team (SLHPT) .
  6. Isolate – as per trust policy
    A patient with known or suspected meningococcal meningitis should be isolated in a single room with droplet precautions for 24 hours from the time that effective antibiotic treatment has been started.
    Staff caring for the patient should observe the standard infection control precautions and wear FFP3 masks, gloves and aprons.
    Staff performing procedures that may generate aerosols, for example suctioning, intubation or inserting an airway, should wear properly fitted FFP3 masks and eye protection.
  7. Antibiotic Prophylaxis for close contacts should be coordinated by SLHPT. OH Assist will coordinate antibiotic prophylaxis for healthcare workers
    Antibiotic prophylaxis is offered to the following groups of people:
  8. Those who have had prolonged close contact with the patient during the seven day incubation period. This includes people who live or sleep in the same household, dormitory or halls of residence.
  9. Intimate (kissing) contacts.
  10. Those exposed transiently to large droplets from the upper respiratory tract of the patient during their admission to hospital. For example, a healthcare-worker inserting an airway or suctioning the upper respiratory tract without wearing appropriate personal protective equipment may be at risk.
References
http://www.journalofinfection.com/article/S0163-4453(16)00024-4/abstract http://www.journalofinfection.com/cms/attachment/2048213088/2058279234/mmc1.pdf
https://www.uptodate.com/contents/viral-encephalitis-in-adults?source=search_result&search=meningitis%20aciclovir&selectedTitle=3~150 http://lgnet/download.cfm?ver=10662
https://www.rcemlearning.co.uk/modules/intracranial-infections/
http://learning.bmj.com/learning/modules/flow/ICH.html?execution=e1s1&moduleId=5003335&status=LIVE&action=start&_flowId=ICH&sessionTimeoutInMin=90&locale=en_GB&shouldStartAtQuestionSection=false
http://learning.bmj.com/learning/modules/flow/ICH.html?execution=e2s1&moduleId=10041919&status=LIVE&action=start&_flowId=ICH&sessionTimeoutInMin=90&locale=en_GB&shouldStartAtQuestionSection=false

Sunday, 14 August 2016

Sepsis

So Sepsis confuses me. There's loads of guidelines we're supposed to follow (some with out of date evidence) and it's not as simple as it could be. I've tried to simplify it... but might easily have misinterpreted something!

Sepsis = life threatening organ dysfunction due to dysregulated host response to infection. “SOFA” helps define and “prove” organ dysfunction. 

CEM and Surviving Sepsis Criteria define with SIRS
Need at least two of:
Temp > 38.3   Temp <36
WCC >12 or WCC <4
HR >90 RR >20
AMS BM >7.7

Patients with at least two SIRS criteria and suspected infective source should have the sepsis six delivered ASAP (within three hours of time of presentation according to surviving sepsis, within an hour if severe sepsis according to RCEM and most trusts).  Surviving sepsis state within six hours of presentation we need vasopressors, re-assessment and re-check of the lactate.

Septic Shock – need vasopressors to keep MAP >65, lactate >2 despite fluid resuscitation. Sepsis 6 – 30mg/ kg for hypotension or lactate >4.

SOFA Scores
New studies have shown that SIRS is non specific and should no longer used for sepsis prognosis. They instead suggest a “SOFA (sepsis related organ failure assessment)” score where a changing score of > 2 = mortality of 10%.
 The Qsofa is a quick bedside alternative, and >2 factors + suspected infection should make you think of sepsis:
"BAT" BP <100
          AMS
                        Tachypnoea RR >22
This has not made its way into national guidelines yet.

RCEM Guidelines 
Screen for sepsis using “SIRS criteria”
Sepsis risk stratify. Start sepsis six immediately if any one of:
SBP <90mmHg or >40mmHg fall from baseline
MAP <65mmHg
Heart rate >130 per minute*
New need for supplemental oxygen to maintain saturations >90% and bilateral infiltrates.
Respiratory rate >25 per minute*
AVPU = V, P or U*
PaO2 / FiO2 ratio <300 (mmHg) or <39.9 (kPa)
Lactate >2.0mmol/L
Creatinine >176.8µmol/L
INR >1.5
aPTT >60s
Platelet count <100 x109/L
Bilirubin >34.2µmol
Urine output <0.5mL/kg for two consecutive hours

Uncomplicated Sepsis: Decide whether to initiate sepsis six or not, >ST4 review within an hour, hourly obs, repeat lactate in two hours.

Red Flag Sepsis: HR > 130, AVPU less than A, RR >25
If blood results not confirmatory for severe sepsis, senior to review.

Red Flag or Severe: Severe sepsis is no longer in the Sepsis definitions but is in the RCEM guideline. Sepsis six ASAP, but within 60 minutes. >ST4 review. Obs 30minly.  Repeat lactate.

Septic Shock: As above. Inform EM Consultant. Refer to outreach.  Persisting hypotension requiring vasopressors to maintain MAP. Blood lactate >2mmol/L despite adequate volume resuscitation.

NICE Guidelines – July 2016
High risk of sepsis: in <1 year and >75 (or very frail). Immunosuppressed – by drugs or disease. Surgery in past six weeks. Breach of skin integrity. IV drug user. Indwelling lines or catheters. Pregnant or <6 weeks post partum.

Risk stratification for 12years and older – history. Respiratory (>25 or >40% FiO2 to keep sats >92% = high. Moderate = RR 21 – 24). BP (High = <90 or >40 below normal. Mod =91 – 100mmg Hg.). Circ (High = HR >130 bpm, anuric 18 hours, <0.5ml/hour if catheterised. Mod = HR 91 – 130 or new arrhythmia. Anuric 12 – 18 hours. 0.5 – 1ml / kg). Temp (Mod = temp <36). Skin (High = mottled or ashen, cyanosis, non blanching rash. Mod = Skin signs of infection).

There is a different stratification for children <5, and aged 5 – 11.

If >1 high risk criteria, senior clinical decision maker to review. Tests for glucose, lactate, cultures, FBC, CRP, U&E, creatinine, clotting. Antibiotics. Discuss with a Consultant. If septic shock, IV fluids stat, and refer to critical care. If lactate 2-4, give IV fluid bolus within an hour. Lactate <2, consider IV fluids. Monitor every 30minly. Consultant to r/v if failure to respond.

CEM Standards – severe sepsis and septic shock
Observe temp, PR, RR, BP, Mental status, BM on arrival.
Senior EM review within an hour
High flow O2 before leaving ED
Lactate, blood cultures
20mls/ kg fluid – 75% within an hour of arrival, 100% before leaving ED. Antibiotics – 50% within an hour, 100% before leaving ED.
Urine output measured before leaving the ED.

Trials
EGDT: Rivers. Found mortality benefit for EGDT.
ProCESS: Looked at protocol resus vs. usual car in septic shock. More ICU admissions in EGDT group. No difference otherwise.
ARISE: Australia. No advantage of EGDT.
PromMISe: UK based. No advantage over EGDT, which also increases costs.

Some theories: busted!
• Activated protein C - doesn't work
• Steroids - don't work, may be a small role only.
• Intensive insulin therapy - was based on harm from hyperglycaemia now used as moderate therapy only.

CRP
C reactive protein (CRP) is a protein produced by the liver in response to triggers from macrophages and adipose cells, which binds to the surface of dead or dying cells to activate the complement system.
CRP will rise within 2 hours of inflammation onset and peak at 48hrs. A normal level of CRP is not truly known.

References and Resources
http://www.rcem.ac.uk/Shop-Floor/Clinical%20Standards/Sepsis
http://www.heftemcast.co.uk/sepsis-in-the-ed/
http://www.heftemcast.co.uk/sepsis-smaccback/
http://www.frca.co.uk/article.aspx?articleid=100855
http://stemlynsblog.org/early-goal-directed-therapy-dead-st-emlyns/
http://www.survivingsepsis.org/SiteCollectionDocuments/SSC_Bundle.pdf http://stemlynsblog.org/the-promise-study-egdt-rip/
http://stemlynsblog.org/surviving-sepsis-update/
http://foam4gp.com/2015/07/23/foam4gp-map-my-esr-is-bigger-than-your-crp-or-do-we-care-not/