Paediatrics videos & books

2022-06-01 07:02:01 The hallmark of immune (also known as idiopathic) thrombocytopenia purpura (ITP) is the otherwise healthy appearing child with isolated thrombocytopenia. ITP is the most common cause of isolated thrombocytopenia in childhood. It occurs with equal frequency in both boys and girls. The presence of thrombocytopenia in a patient with otherwise normal cell lines, and a normal physical examination is enough to make the diagnosis, so further evaluation, such as a bone marrow biopsy, is unnecessary. Which children to treat and which treatment to use are areas of controversy in the management of ITP. Most acute ITP will resolve spontaneously, so many will recommend observation for children who appear well, are asymptomatic, and have platelet counts above 30,000. Platelet transfusions should be reserved only in the instance of ongoing or imminent bleeding. When a decision is made to treat, usually when the platelet count falls below 20,000, there are several options available. Treatment involves using IVIG, steroids, anti-D immunoglobulins, or combinations thereof. Combinations of medications may work synergistically. Prednisone is often used initially, as it can be given orally and is inexpensive. Typically, it will be tapered over 2 weeks to 3 months. By using combination therapy when needed, splenectomy can be avoided in the vast majority of cases. When it is necessary, it should be delayed, if at all possible, for at least a year after diagnosis. Open / Comment

2022-05-31 07:01:46 59) Following your initial evaluation and treatment, you see the child for follow-up in 1 week. She continues to appear well but still has obvious purpura and her platelet count is now 17,000. All other cell lines are normal. Of the options listed below, what… Open / Comment

2022-05-31 06:58:47 59) Following your initial evaluation and treatment, you see the child for follow-up in 1 week. She continues to appear well but still has obvious purpura and her platelet count is now 17,000. All other cell lines are normal. Of the options listed below, what is your most appropriate management at this time?
(A) admission to the regional children’s hospital for a platelet transfusion
(B) admission to the children’s hospital for a splenectomy
(C) reassurance to the parents and close outpatient follow-up
(D) admission to the children’s hospital for IVIG and steroids
(E) whole-blood transfusion with several hours of observation to ensure that there is no transfusion reaction Open / Comment

2022-05-26 19:16:01 The hallmark of immune (also known as idiopathic) thrombocytopenia purpura (ITP) is the otherwise healthy appearing child with isolated thrombocytopenia. ITP is the most common cause of isolated thrombocytopenia in childhood. It occurs with equal frequency in both boys and girls. The presence of thrombocytopenia in a patient with otherwise normal cell lines, and a normal physical examination is enough to make the diagnosis, so further evaluation, such as a bone marrow biopsy, is unnecessary. Which children to treat and which treatment to use are areas of controversy in the management of ITP. Most acute ITP will resolve spontaneously, so many will recommend observation for children who appear well, are asymptomatic, and have platelet counts above 30,000. Platelet transfusions should be reserved only in the instance of ongoing or imminent bleeding. When a decision is made to treat, usually when the platelet count falls below 20,000, there are several options available. Treatment involves using IVIG, steroids, anti-D immunoglobulins, or combinations thereof. Combinations of medications may work synergistically. Prednisone is often used initially, as it can be given orally and is inexpensive. Typically, it will be tapered over 2 weeks to 3 months. By using combination therapy when needed, splenectomy can be avoided in the vast majority of cases. When it is necessary, it should be delayed, if at all possible, for at least a year after diagnosis. Open / Comment

2022-05-25 19:15:40 Open / Comment

2022-05-21 11:18:46 #NEETPG2022 Posting
NEET PG 22 Recall questions & Discussion
join @doctorusmle Now Open / Comment

2022-05-20 11:16:01 The hallmark of immune (also known as idiopathic) thrombocytopenia purpura (ITP) is the otherwise healthy appearing child with isolated thrombocytopenia. ITP is the most common cause of isolated thrombocytopenia in childhood. It occurs with equal frequency in both boys and girls. The presence of thrombocytopenia in a patient with otherwise normal cell lines, and a normal physical examination is enough to make the diagnosis, so further evaluation, such as a bone marrow biopsy, is unnecessary. Which children to treat and which treatment to use are areas of controversy in the management of ITP. Most acute ITP will resolve spontaneously, so many will recommend observation for children who appear well, are asymptomatic, and have platelet counts above 30,000. Platelet transfusions should be reserved only in the instance of ongoing or imminent bleeding. When a decision is made to treat, usually when the platelet count falls below 20,000, there are several options available. Treatment involves using IVIG, steroids, anti-D immunoglobulins, or combinations thereof. Combinations of medications may work synergistically. Prednisone is often used initially, as it can be given orally and is inexpensive. Typically, it will be tapered over 2 weeks to 3 months. By using combination therapy when needed, splenectomy can be avoided in the vast majority of cases. When it is necessary, it should be delayed, if at all possible, for at least a year after diagnosis. Open / Comment

2022-05-20 11:11:01 The hallmark of immune (also known as idiopathic) thrombocytopenia purpura (ITP) is the otherwise healthy appearing child with isolated thrombocytopenia. ITP is the most common cause of isolated thrombocytopenia in childhood. It occurs with equal frequency in both boys and girls. The presence of thrombocytopenia in a patient with otherwise normal cell lines, and a normal physical examination is enough to make the diagnosis, so further evaluation, such as a bone marrow biopsy, is unnecessary. Which children to treat and which treatment to use are areas of controversy in the management of ITP. Most acute ITP will resolve spontaneously, so many will recommend observation for children who appear well, are asymptomatic, and have platelet counts above 30,000. Platelet transfusions should be reserved only in the instance of ongoing or imminent bleeding. When a decision is made to treat, usually when the platelet count falls below 20,000, there are several options available. Treatment involves using IVIG, steroids, anti-D immunoglobulins, or combinations thereof. Combinations of medications may work synergistically. Prednisone is often used initially, as it can be given orally and is inexpensive. Typically, it will be tapered over 2 weeks to 3 months. By using combination therapy when needed, splenectomy can be avoided in the vast majority of cases. When it is necessary, it should be delayed, if at all possible, for at least a year after diagnosis. Open / Comment

2022-05-19 11:10:30 58) A well-appearing 6-year-old presents to your office with a chief complaint of bruising. The parents report that the child had a cold 2 weeks ago but completely recovered. The child is sitting on the examining table, in no distress, discussing her favorite… Open / Comment

2022-05-19 11:09:02 58) A well-appearing 6-year-old presents to your office with a chief complaint of bruising. The parents report that the child had a cold 2 weeks ago but completely recovered. The child is sitting on the examining table, in no distress, discussing her favorite cartoons. On examination, you find mucosal bleeding and bruises on the child’s arms and chest. You order a complete blood count (CBC) that has the following results: WBC 12,000, hemoglobin 11 g/dL, and a platelet count of 45,000. What is the most likely cause of this child’s bleeding and bruising? Open / Comment