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1.
J Pak Med Assoc ; 73(8): 1663-1666, 2023 Aug.
Article in English | MEDLINE | ID: mdl-37697759

ABSTRACT

OBJECTIVE: To evaluate whether or not the pre-infusion checklist for rituximab was followed in patients of pemphigus vulgaris. Method: The audit, intervention and re-audit was conducted at the Dermatology Department, Medical Teaching Institution-Lady Reading Hospital, Peshawar, Pakistan, and comprised in-patients of pemphigus vulgaris, confirmed by skin biopsy and immunofluorescence, who received rituximab between January 1 to March 31, 2022. The randomly picked cases were reviewed to check if the standard guidelines for rituximab prior to infusion had been followed. After completion of the first audit cycle, the medical team was give awareness about the latest pre infusion rituximab guidelines, and they were also provided with a checklist and consent form to implement the change. Re-audit was performed from May to July, 2022, using the same method to see if improvements had been made. Data was analysed using SPSS 23. RESULTS: Of the 20 cases evaluated against 16 parameters, the first audit showed 7(43.5%) parameters to have been met across all cases. Re-audit comprised another set of 20 cases, and showed that 15(93.75%) parameters had been applied across the board Pneumococcal and influenza vaccine was the only element 1(6.25%) not touching universal application. CONCLUSIONS: Re-audit showed major improvement in compliance with the standard guidelines.


Subject(s)
Pemphigus , Humans , Pemphigus/drug therapy , Checklist , Rituximab/therapeutic use , Clinical Audit , Hospitals, Teaching
2.
J Pak Med Assoc ; 73(7): 1539-1541, 2023 Jul.
Article in English | MEDLINE | ID: mdl-37469078

ABSTRACT

Juvenile dermatomyositis (JDM) is a rare autoimmune disease characterised by inflammation of muscles and skin with extra muscular involvement of joints, heart, intestine, and liver. Pathogenesis of JDM is believed to be due to vasculopathy. Along with classic cutaneous features of JDM, rare findings include hypertrichosis, lipoatrophy, photosensitivity, bullous lesions, and hyperhidrosis. We present, here, a case of JDM with hypertrichosis as very few cases have been reported previously.


Subject(s)
Dermatomyositis , Hypertrichosis , Vascular Diseases , Humans , Dermatomyositis/complications , Dermatomyositis/diagnosis , Hypertrichosis/diagnosis , Hypertrichosis/etiology , Hypertrichosis/pathology , Skin/pathology , Inflammation/pathology
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