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Consortium for Pharmaceutical Education and Practice Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Consortium for Pharmaceutical Education and Practice, Hospital Road, Taluk Headquarters Hospital, Peermade.

The Consortium for Pharmaceutical Education and Practice (CPEP) is a professional hub for Pharmacy Practising Professionals to update and educate on their day to day assignments.

Hâ‚‚RAs or PPIs? Choosing the right acid-suppressive therapy depends on the clinical indication, symptom burden and patien...
01/11/2026

Hâ‚‚RAs or PPIs? Choosing the right acid-suppressive therapy depends on the clinical indication, symptom burden and patient-specific factors.

This review covers their pharmacology, clinical indications, combination therapy, important drug interactions, safety considerations and appropriate PPI deprescribing.

A practical reference for clinical pharmacists and healthcare professionals involved in gastrointestinal pharmacotherapy.

HRS-AKI: A practical approach to clinical managementManaging hepatorenal syndrome–acute kidney injury (HRS-AKI) requires...
25/10/2026

HRS-AKI: A practical approach to clinical management

Managing hepatorenal syndrome–acute kidney injury (HRS-AKI) requires timely diagnosis, appropriate vasoconstrictor therapy, careful monitoring and decisions around renal replacement therapy.

This carousel covers key management points, including vasoconstrictor alternatives, when to consider RRT, modality selection, and the role of liver transplantation.

A focused clinical reference for healthcare professionals involved in the care of patients with cirrhosis and HRS-AKI.

-AKI

Burn care involves much more than treating the wound. From the first minutes of assessment to fluid resuscitation, dress...
22/10/2026

Burn care involves much more than treating the wound. From the first minutes of assessment to fluid resuscitation, dressing selection, infection prevention and rehabilitation, every decision can influence healing and long-term function.

This CPEP clinical reference brings together key principles of burn assessment and management for healthcare professionals, with a focus on practical decisions, early recognition of complications and timely specialist involvement.

Save this carousel for your clinical reference, and share it with colleagues involved in emergency care, clinical pharmacy and burn management.

How to switch between statins: dose equivalence and what to check nextSwitching from one statin to another requires more...
19/10/2026

How to switch between statins: dose equivalence and what to check next

Switching from one statin to another requires more than matching milligram doses. The expected LDL-C reduction, drug interactions, tolerability and the patient’s cardiovascular risk all matter.

This CPEP guide covers: • Atorvastatin and rosuvastatin dose comparisons • How simvastatin compares with rosuvastatin • Dose intensity of other commonly used statins • Important drug interactions and safety considerations • When to repeat the lipid profile and reassess treatment

Use the comparisons as a clinical reference, not as an exact milligram-for-milligram conversion. After switching, reassess the lipid response in 4–12 weeks and adjust treatment according to the patient’s risk and guideline-recommended goals.

Reference: 2026 ACC/AHA Multisociety Guideline on the Management of Dyslipidemia; VOYAGER meta-analysis.

P-CABs vs PPIs: Understanding vonoprazan in clinical practiceHow do potassium-competitive acid blockers differ from PPIs...
15/10/2026

P-CABs vs PPIs: Understanding vonoprazan in clinical practice

How do potassium-competitive acid blockers differ from PPIs, and what does stronger acid suppression mean for patient care?

This 5-slide review covers P-CAB pharmacology, intragastric pH data, clinical evidence in erosive oesophagitis, H. pylori eradication and NERD, plus practical vonoprazan dosing considerations.

Greater acid suppression does not automatically mean better outcomes in every clinical setting. Evidence and prescribing decisions remain indication-specific.

**ESR, CRP or Procalcitonin? A clinical guide to interpretation**ESR, CRP and procalcitonin (PCT) are commonly used in c...
13/10/2026

**ESR, CRP or Procalcitonin? A clinical guide to interpretation**

ESR, CRP and procalcitonin (PCT) are commonly used in clinical practice, but they answer different questions. Knowing when to order them—and how to interpret the result in context—is just as important as the value itself.

**ESR** changes relatively slowly and is influenced by factors such as age, anaemia, pregnancy and renal disease. It may be useful in selected chronic inflammatory conditions, but is less suited to assessing rapid changes.

**CRP** responds more quickly to inflammation and can help assess the clinical trajectory. However, infection is only one of many causes of an elevated CRP, and a low early result does not exclude an evolving infection.

**Procalcitonin (PCT)** can support antibiotic-stewardship decisions in selected patients. In adults with sepsis or septic shock, the 2026 Surviving Sepsis Campaign suggests using PCT alongside clinical evaluation to help guide antibiotic discontinuation when the optimal duration is unclear and source control is adequate. PCT should not replace clinical assessment when deciding whether to initiate antibiotics.

In practice, interpret all three markers alongside the history, examination, microbiology, timing of sampling and response to treatment. An isolated result rarely tells the whole story.

CKD + Type 2 Diabetes: The 2026 Treatment UpdateManaging diabetic kidney disease requires more than glycaemic control. T...
10/10/2026

CKD + Type 2 Diabetes: The 2026 Treatment Update

Managing diabetic kidney disease requires more than glycaemic control. The 2026 approach focuses on preserving kidney function, reducing cardiovascular risk and selecting therapies according to eGFR, albuminuria and individual patient needs.

In this clinical carousel, we cover the decisions that matter in practice:

🔹 **eGFR + UACR:** Assess kidney function and albuminuria to stratify risk and guide treatment.

🔹 **SGLT2 inhibitors:** Prioritise agents with proven kidney and cardiovascular benefits when indicated.

🔹 **ACE inhibitors/ARBs:** Optimise renin–angiotensin system blockade in patients with hypertension and albuminuria.

🔹 **Finerenone:** Address residual albuminuric risk in eligible patients despite maximally tolerated ACEi/ARB therapy.

🔹 **GLP-1 receptor agonists:** Understand the cardiovascular benefits and evolving kidney-outcome evidence, including the FLOW trial of semaglutide.

The central principle is to use complementary therapies where indicated, monitor treatment response and individualise decisions according to kidney function, potassium, cardiovascular risk and tolerability.

**For clinicians managing T2DM with CKD, these are important treatment decisions to revisit in 2026.**

MASLD/MASH: 2026 Clinical UpdateThe management of MASLD and MASH continues to evolve, with greater emphasis on identifyi...
05/10/2026

MASLD/MASH: 2026 Clinical Update

The management of MASLD and MASH continues to evolve, with greater emphasis on identifying patients at risk of progressive fibrosis, addressing cardiometabolic risk factors and selecting appropriate treatment.

For healthcare professionals, clinical management extends beyond treatment initiation. Follow-up should include assessment of weight, glycaemic control, lipid profile, liver biochemistry, treatment tolerability and relevant drug interactions. Non-invasive tests can help reassess fibrosis risk when interpreted alongside the patient's clinical findings.

An important point in practice: improvements in liver enzymes or body weight alone do not confirm MASH resolution or fibrosis regression. Treatment response and safety should be assessed using the relevant clinical guidance and prescribing information.

This carousel brings together key clinical considerations for the assessment, treatment and follow-up of MASLD/MASH, including current evidence on semaglutide and resmetirom.

Save this reference for clinical practice and share it with colleagues involved in metabolic and liver disease care.

β-Lactam Antibiotics: 2026 UpdateOptimising β-lactam therapy in critically ill patients requires attention to pharmacoki...
03/10/2026

β-Lactam Antibiotics: 2026 Update

Optimising β-lactam therapy in critically ill patients requires attention to pharmacokinetic variability, PK/PD targets and the infusion strategy. Sepsis, altered volume of distribution and changes in renal clearance can affect antibiotic exposure, making dose individualisation and therapeutic drug monitoring relevant in selected patients.

This update reviews practical approaches to β-lactam dose individualisation, TDM sampling and model-informed precision dosing. It also examines the 2026 focused update on prolonged infusion: in severely ill adults, particularly those with Gram-negative infections, prolonged infusion is suggested over short infusion. The pooled analysis reported lower mortality (RR 0.91; 95% CI 0.85–0.97; 28 RCTs) and higher clinical cure (RR 1.11; 95% CI 1.06–1.17; 21 RCTs). The recommendation is conditional, with moderate-certainty evidence for mortality and low-certainty evidence for clinical cure.

A practical reference for clinicians involved in antimicrobial prescribing, critical care and antimicrobial stewardship.

INOTROPES | A practical haemodynamic approachInotropes are not simply “drugs that increase cardiac output.” Their role d...
01/10/2026

INOTROPES | A practical haemodynamic approach

Inotropes are not simply “drugs that increase cardiac output.” Their role depends on the underlying haemodynamic problem, the presence of tissue hypoperfusion, arterial pressure, vascular tone, and the patient’s response to treatment.

This 4-slide clinical guide covers:
• When inotropic therapy should be considered
• Cardiac output, arterial pressure and tissue perfusion
• Choosing between inotropes, vasopressors and inodilators
• SCAI Shock Classification A–E
• Key principles for monitoring response and reassessment

For clinicians managing cardiogenic shock, understanding the haemodynamic phenotype is essential for selecting vasoactive therapy and avoiding unnecessary exposure to its risks.

Save this for ward rounds, emergency assessment and cardiogenic shock management.

Address

Hospital Road, Taluk Headquarters Hospital
Peermade
685531

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm
Saturday 9am - 5pm

Telephone

+919895137331

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