Skip to content
V

Vaishali Tembhare

Publications (4)

Nursing Skill and Responsibility in Administration of Low Molecular Weight Heparin by Prefilled Syringe

Vaishali Tembhare, Gaurav Mujbaile, Seema Singh, Achita Sawarkar, Maduri Shambharkar & Prerana Sakharwade · Journal of Pharmaceutical Research International · 2021

Abstract: Low-molecular-weight heparins (LMWHs) have proven to be effective in the prevention and treatment of thrombotic disorders, as well as   substitute for unfractionated heparin (UFH). LMWHs are a diverse collection of medicines with different biochemical and pharmacologica...

Open access Research Article 10.9734/jpri/2021/v33i47A32993

Effectiveness of Structured Teaching on Nursing Students’ Knowledge Regarding Light Pollution in a College at Wardha

Pallavi Patil & Vaishali Tembhare · Asian Journal of Environment & Ecology · 2026

Introduction: Light pollution, also referred to as photo pollution, occurs when excessive artificial light from human-made sources enters the atmosphere, particularly the troposphere. It contributes to environmental degradation, disrupts circadian rhythms, affects nocturnal wildl...

Open access Research Article 10.9734/ajee/2026/v25i7978

Case Report on Sacroccygeal (Teratomas) Germ Cell Tumor

Payal Nanotkar, Vaishali Tembhare, Khushabu Meshram, Pooja Kasturkar, Savita Pohekar, Jaya Khandar, Samrudhi Gujar & Achita Sawarkar · Journal of Pharmaceutical Research International · 2021

Sacrococcygeal teratomas are a type of germ cell tumour (GCTs) accounting for 40% of all GCTs of all GCT,s in children. Interestingly 75% occurs in females. Reporting here a case of 3 years old female baby hospitalized for surgical excision of sacrococcygeal teratoma. A female (3...

Open access Research Article 10.9734/jpri/2021/v33i47A33063

Effectiveness of Planned Teaching on Knowledge Regarding Noonan Syndrome among Nursing Students

Pragati Alnewar, Seema Singh & Vaishali Tembhare · Journal of Pharmaceutical Research International · 2021

Background: Noonan syndrome is a genetic multisystem disorder characterized by distinctive facial features, developmental delay, learning difficulties, short stature, congenital heart disease, renal anomalies, lymphatic malformation and bleeding difficulties, mutations that cause...

Open access Research Article 10.9734/jpri/2021/v33i47A33065