Specialist Pediatric Palliative Care Prescribing Practices: A Large 5-year Retrospective Audit

Anuja Damani1, Naveen Salins1, Arunangshu Ghoshal1

  • 1Department of Palliative Medicine, Tata Memorial Hospital, Mumbai, Maharashtra, India.

Insights

This audit of pediatric palliative care prescribing in India found significant noncompliance with WHO guidelines and poor use of generic names. Enhanced prescriber and patient education is crucial for effective symptom management in children with cancer.

Area of Science:

  • Oncology
  • Palliative Care
  • Pharmacology

Background:

  • Childhood cancer incidence is rising in India, highlighting the need for specialized pediatric palliative care.
  • Effective symptom management in pediatric cancer patients relies on precise knowledge of palliative care formularies, dosing, and guidelines.
  • This study retrospectively audited prescribing practices within a tertiary cancer center's specialist pediatric palliative care service.

Purpose of the Study:

  • To evaluate prescribing practices for pain and symptom control in children with advanced cancer receiving specialist palliative care.
  • To identify areas of noncompliance with established prescribing guidelines.
  • To assess the documentation of adverse drug events and patient compliance.

Main Methods:

  • A retrospective audit of 1135 medication records from children in specialist pediatric palliative care services.
  • Data collected over a 5-year period (2010-2014).
  • Analysis focused on drug types, quantities, adherence to guidelines, and documentation.

Main Results:

  • 51 drug types were prescribed, averaging 4.2 per prescription. Paracetamol (66.9%) and morphine (33.9%) were common. Ibuprofen was the most frequent NSAID (23.9%).
  • Over 50% of prescriptions included aperients, commonly a liquid paraffin and sodium-picosulfate combination. Dexamethasone was used in 51.9% of patients, often with oral chemotherapy.
  • Only 33% of prescriptions used generic names, and adverse effects were documented in just 9%. Noncompliance with WHO guidelines occurred in 25% of cases, with patient compliance at 40%.

Conclusions:

  • Knowledge of pediatric palliative care formulary, rational drug use, and dosing guidelines is vital for symptom control in children with life-limiting illnesses.
  • Poor prescribing practices, including noncompliance with WHO guidelines (25%) and infrequent use of generic names (33%), necessitate prescriber education.
  • Alarming patient noncompliance (nearly 66%) underscores the need for intensive patient, family, and caregiver education and empowerment.
Abstract

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