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25/01/2025
04/11/2024

Relevant Queries on Piperacillin-Tazobactam (Piptaz) Dosing and Use
( this post is in response to a comment on previous fluid therapy post )

Here are some frequently asked questions regarding the use of Piptaz in critical and ward and surgical care:

Query 1:
“I’ve seen Piptaz given twice, three times, or even QID (four times daily). What’s the ideal dosing regimen for critically ill patients?”

Answer:
In critically ill patients, especially those on fluids or vasopressors, augmented renal clearance (ARC) can increase drug elimination rates, which can lead to lower antibiotic concentrations if dosed inadequately.

• Critically Ill Patients with ARC: Typically, QID (four times daily) dosing is ideal. Patients with high BMI (>40), weight >120 kg, cystic fibrosis, high MIC infections, or deep-seated/nosocomial infections may need this higher frequency or extended infusions to maintain effective drug concentrations.
• Stable Ward Patients: For patients without ARC, TID (three times daily) may be sufficient.

Query 2:
“Should we add metronidazole to Piptaz for anaerobic coverage in surgical and other patients?”

Answer:
For most cases, adding metronidazole to Piptaz is unnecessary because Piptaz alone provides comprehensive anaerobic coverage. Doubling with metronidazole offers no additional benefit and only increases the risk of side effects.

However, there are specific scenarios where metronidazole may be warranted. For instance, in cases of amoebic liver abscess, metronidazole can be added to Piptaz, as it targets the amoebic infection effectively. This is an exception rather than the norm, so consider it only when the clinical scenario justifies it.

Query 3:
“Is every gram-positive infection MRSA, and should we always cover for MRSA empirically. Does piptaz need gram positive cover if it is not MRSA ??

Answer:
Not all gram-positive infections are MRSA. MRSA coverage should only be considered in patients with particular risk factors, such as prolonged hospitalizations, recent surgeries, indwelling catheters, immunosuppression, or a known history of MRSA. Empirical MRSA treatment should be reserved for these high-risk cases or initiated if culture results confirm MRSA.
Piptaz has good gram positive cover expect MRSA .. so it doesn’t need VANCO in the name of gram positive cover .. please avoid this harm 90 percent times when we add vanco over piptaz there is no risk or infection with MRSA .. we are again doubling gram positive cover unnecessarily

Query 4:
“Should we adjust antibiotics like Piptaz or Meropenem according to renal clearance from day one in life-threatening infections?”

Answer:
In cases of life-threatening infections, adjusting antibiotics based on renal clearance from the outset is generally not recommended for 24 to 48 hours initially give full dose ..Here’s why:

1. Data Limitation: Most creatinine-based dosing adjustments are derived from studies in patients with Chronic Kidney Disease (CKD) and End-Stage Renal Disease (ESRD), not for Acute Kidney Injury (AKI). AKI is a highly dynamic condition, with renal function that can fluctuate significantly, unlike the relatively stable nature of CKD.
2. Delayed Creatinine Response: Serum creatinine, commonly used to estimate renal function, often lags by about 48 hours behind real-time changes. Relying on creatinine for immediate adjustments can lead to inaccurate dosing based on outdated renal status.
3. Risk of Underdosing: Due to these limitations, adjusting doses too soon can result in subtherapeutic drug levels, especially in the critically ill, where up to 50% of patients may fail to achieve necessary antibiotic concentrations early on. This underdosing heightens the risk of treatment failure, which can be life-threatening in severe infections.

To optimize outcomes, it is advisable to maintain full dosing during the first 1-2 days for critically ill patients. This approach helps ensure that severe infections—such as septic shock—are managed effectively upfront. After this initial period, once the patient stabilizes, renal and other organ functions can be reassessed, and dosing adjustments can be made accordingly.

QUESTION TIME 🔻With successful intubation after 2 laryngoscopic attempts with 2mcg/kg fentanyl, 0.2mg/kg Etomidate and 2...
06/06/2024

QUESTION TIME 🔻
With successful intubation after 2 laryngoscopic attempts with 2mcg/kg fentanyl, 0.2mg/kg Etomidate and 2.5mg/kg scoline, the patient gets bradycardia with a heart rate of 36 bpm.
What is the most likely cause ?
A. Hypoxia
B. Hypercapnia
C.Reflex bradycardia from sympathetic stimulation
D. SA node dysfunction
E. Succinylcholine

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