Question from S 14 Flashcards

1
Q

Verbal actual

What are the challenges of IP&C and clinical management, in the absence of test results (pretend testing has been discontinued)

How would you manage these challenges?

A

Summarise problem - without diagnostic testing, there will be a significant impact on IP&C and management of patients.

This will include:
increased HAI/outbreaks
delayed discharge
increased Abx use
inappropriate anti-viral use
increased morbidity/ mortality

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2
Q

Verbal actual

What are the challenges of IP&C and clinical management, in the absence of test results (pretend testing has been discontinued)

How would you manage these challenges?
potential solutions

A

Management:

cohort patients by symptoms/ clinical syndrome and local epidemiological data

High risk patients (immunosuppressed) - put in side rooms as high risk of acquiring HAI

Update IP&C guidelines to reflect new practice

Consider sending a few samples as send-away tests, to establish outbreaks in your hospital e.g local network hospitals/ reference labs

Communicate new guidelines to stakeholders - IPC/ A&E/ GP etc

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3
Q

Verbal actual

Absence of clinical test results

What regulations do this break?
Who would you inform?

A

UKAS/ UKHSA

Inform them early, so they are aware of circumstances.
Including change to plan or change of assay

If a long term issue, need to tell them about change to our assay/method and scope of testing

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4
Q

Verbal actual

Absence of clinical test results due to supply chain issue

How will you review your policies after this incident?

A

I will learn from the event, and adapt so our service has greater resilience and flexibility

To build in resilience:
- increase stock of reagents, if storage allows
- avoid single-chain bottle necks - e.g only 1 supplier of reagent
- multi-channel supply chain contingencies
- review whether switching suppliers/ assays is warranted
- inter-tendencies with neighbouring lab networks
- review communication network for cascading information
- review current contingency plans
- communicateto UKAS

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5
Q

Verbal actual

39F admit to A&E
dry cough, SOB, myalgia
Inhaled steroids for asthma
No other PMHx

Respiratory viral PCR swab - A H1N1 pos

Requires admission

how would you manage this case?

History
Diagnosis
Management
IP&C
Public Health

A

Summarise case
- 39F on inhaled steroids, admitted with acute respiratory symptoms, and confirmed Influenza A H1N1 on testing

Clinical history
unwell contacts
travel
animal exposure e.g Avian influenza
recurrent infections - needs HIV test
sputum production - Influenza with secondary bacterial infection
Annual influenza vaccine

Diagnosis
CXR - bilateral interstitial pneumonia
Swab - check no other viral infections
Sputum culture
FBC - lymphopenia/ lymphocytosis
UE - check renal function if giving antiviral
HIV test

Management
Oseltamivir 75mg BD for 5 days
Start within 48 hours, consider up to 5 days as has lung condition

IP&C
side room - respiratory precautions
FFP3 if AGP performed

Public Health
Notify automatically by lab reporting

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6
Q

Verbal actual

Who 6x patient groups are indicated to have influenza PEP?

A

Age >65, Age <6 months
Pregnant women - up to 2 months post-partem
Chronic lung/ heart/ kidney/ liver conditions
Diabetes
Immunosuppressed
Morbid obesity - BMI >40
Asplenia

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7
Q

Verbal actual

What is oseltamivir PEP dosing based on?

A

Renal function

Weight - standard 75mg dosing based on >41kg

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8
Q

Verbal actual

What drugs are used as influenza PEP?

A

Oseltamavir

Use inhaled zanamavir if:
- local resistance reports high rates of oseltamivir resistance
- if severely immunosuppressed

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9
Q

Verbal actual

When does influenza treatment need to be initiated?

A

Within 48 hours of symptom onset

Can be up to 5 days if patients are high risk

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10
Q

Verbal actual

When does influenza PEP need to be initiated?

A

Start within 48 hours of last contact when patient was infectious

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11
Q

Verbal actual

Patient is influenza A contact

They had their routine annual influenza vaccine

Do they still require PEP?

A

Vaccine considered protective if:

  • it is a good match for circulating variants
  • it has been 14 days since immunisation date

If not, then give oseltamivir

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12
Q

Verbal actual

39F admit to A&E
dry cough, SOB, myalgia
Inhaled steroids for asthma
No other PMHx

Respiratory viral PCR swab - A H1N1 pos

Her 5 year old child presents to ED with URTI symptoms

Swab:
Influenza A H1N1 positive
Influenza A H3N2 positive
Influenza B positive

What is the most likely interpretation of these results?

A

Swab:
Influenza A H1N1 positive
Influenza A H3N2 positive
Influenza B positive

Likely reflects recent administration of Live intranasal vaccine

Other possibility is a triple co-infection

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13
Q

Verbal actual

Her 5 year old child presents to ED with URTI symptoms

Swab:
Influenza A H1N1 positive
Influenza A H3N2 positive
Influenza B positive

What is the most likely reason the child has symptoms?

A

Mother has H1N1 proven, and child is a contact

Therefore likely child has true H1N1 infection

Likely not protected, as it has not been 14 days since vaccine administration

Other possibility is URTI due to vaccine itself

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14
Q

Verbal actual

Her 5 year old child presents to ED with URTI symptoms

Swab:
Influenza A H1N1 positive
Influenza A H3N2 positive
Influenza B positive

Suspect child has H1N1 true infection, as mother has proven infection

How would you prove this?

A

History of timing of vaccine will hint at the diagnosis

  1. Check the respiratory PCR worksheet

Expect:
Influenza A H1N1 to have early take off
Influenza A H3N2/ B to have late-take off

Melt curves from wild type virus, and vaccine may be different

  1. Can send respiratory samples to the Respiratory Virus Unit in Colindale for sequencing
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