The overall nursing care provided to the patient was rated as GOOD based on the computation using the rating scale. Areas that can be improved include pain management and patient education. Continued monitoring and evaluation is recommended.
- Please continue to monitor patient closely and follow up on any labs or tests ordered. Maintain NPO status, IV fluids, medications and rest as directed to support recovery from surgery. Contact medical team promptly if any concerns arise.
this presentation is comparative study on patient. this presentation provide detail and comprehensive knowledge about fracture, its complication as well as fracture of shaft of femur and its treatment and nursing management
Spina bifida is a condition that affects the spine and is usually apparent at birth. It is a type of neural tube defect (NTD). Spina bifida can happen anywhere along the spine if the neural tube does not close all the way.
Spina bifida is a birth defect where the spinal cord fails to close properly, leaving it exposed. There are three main types: spina bifida occulta, which has no protrusion and is usually asymptomatic; meningocele, which involves protrusion of meninges and cerebrospinal fluid in a sac; and myelomeningocele, the most severe form, which involves protrusion of meninges, spinal cord, and cerebrospinal fluid. Treatment involves surgery to close the defect as well as management of any related conditions like hydrocephalus or paralysis. Parents are counseled and trained to care for the child's lifelong medical needs.
Spina bifida is a birth defect where the spine and spinal cord do not form properly, leaving an opening in the spine. It occurs in about 1-2 per 1000 live births. There are three main types: spina bifida occulta which has no symptoms, meningocele which is a sac protruding from the spine containing fluid and membranes, and myelomeningocele which is the most severe form where the spinal cord and membranes protrude out. Treatment depends on the type but may include surgery to close the opening after birth along with management to prevent infections and complications.
Central nervous system defects include disorders caused by an imbalance of cerebrospinal fluid (as in hydrocephalus) and a range of disorders resulting from malformations of the neural tube during embryonic development (often called “neural tube defects”). These defects vary from mild to severely disabling.
Spina bifida is a birth defect where there is an incomplete closing of the backbone and membranes around the spinal cord. It is a developmental congenital anomaly
Patient P.V., a 74-year-old male, presented with progressive body weakness that began 15 days prior. He reported weakness starting in his lower extremities and progressing upwards. He was admitted to the hospital with a chief complaint of body weakness and a diagnosis of Guillain-Barré syndrome was considered. Guillain-Barré syndrome is an autoimmune disorder where the body's immune system attacks the peripheral nervous system, causing muscle weakness and possible paralysis. Nursing care involved assessing the patient, administering medications to treat the condition, providing respiratory support if needed, and patient/family education on Guillain-Barré syndrome and its management.
Spina bifida is a birth defect where the spinal column does not fully close around the spinal cord. It occurs when the neural tube fails to close properly during early embryonic development. The main types are spina bifida occulta (mildest), meningocele (meninges protrude through opening), and myelomeningocele (most severe where spinal cord and membranes protrude). Symptoms range from minor skin marks to paralysis depending on location and severity of the defect. Treatment involves surgery to cover the exposed tissues and may include shunts to drain excess cerebrospinal fluid. Lifelong management focuses on rehabilitation, prevention of infections and complications, and addressing mobility, bladder, and bowel issues.
- Please continue to monitor patient closely and follow up on any labs or tests ordered. Maintain NPO status, IV fluids, medications and rest as directed to support recovery from surgery. Contact medical team promptly if any concerns arise.
this presentation is comparative study on patient. this presentation provide detail and comprehensive knowledge about fracture, its complication as well as fracture of shaft of femur and its treatment and nursing management
Spina bifida is a condition that affects the spine and is usually apparent at birth. It is a type of neural tube defect (NTD). Spina bifida can happen anywhere along the spine if the neural tube does not close all the way.
Spina bifida is a birth defect where the spinal cord fails to close properly, leaving it exposed. There are three main types: spina bifida occulta, which has no protrusion and is usually asymptomatic; meningocele, which involves protrusion of meninges and cerebrospinal fluid in a sac; and myelomeningocele, the most severe form, which involves protrusion of meninges, spinal cord, and cerebrospinal fluid. Treatment involves surgery to close the defect as well as management of any related conditions like hydrocephalus or paralysis. Parents are counseled and trained to care for the child's lifelong medical needs.
Spina bifida is a birth defect where the spine and spinal cord do not form properly, leaving an opening in the spine. It occurs in about 1-2 per 1000 live births. There are three main types: spina bifida occulta which has no symptoms, meningocele which is a sac protruding from the spine containing fluid and membranes, and myelomeningocele which is the most severe form where the spinal cord and membranes protrude out. Treatment depends on the type but may include surgery to close the opening after birth along with management to prevent infections and complications.
Central nervous system defects include disorders caused by an imbalance of cerebrospinal fluid (as in hydrocephalus) and a range of disorders resulting from malformations of the neural tube during embryonic development (often called “neural tube defects”). These defects vary from mild to severely disabling.
Spina bifida is a birth defect where there is an incomplete closing of the backbone and membranes around the spinal cord. It is a developmental congenital anomaly
Patient P.V., a 74-year-old male, presented with progressive body weakness that began 15 days prior. He reported weakness starting in his lower extremities and progressing upwards. He was admitted to the hospital with a chief complaint of body weakness and a diagnosis of Guillain-Barré syndrome was considered. Guillain-Barré syndrome is an autoimmune disorder where the body's immune system attacks the peripheral nervous system, causing muscle weakness and possible paralysis. Nursing care involved assessing the patient, administering medications to treat the condition, providing respiratory support if needed, and patient/family education on Guillain-Barré syndrome and its management.
Spina bifida is a birth defect where the spinal column does not fully close around the spinal cord. It occurs when the neural tube fails to close properly during early embryonic development. The main types are spina bifida occulta (mildest), meningocele (meninges protrude through opening), and myelomeningocele (most severe where spinal cord and membranes protrude). Symptoms range from minor skin marks to paralysis depending on location and severity of the defect. Treatment involves surgery to cover the exposed tissues and may include shunts to drain excess cerebrospinal fluid. Lifelong management focuses on rehabilitation, prevention of infections and complications, and addressing mobility, bladder, and bowel issues.
A baby girl born at 38 weeks was diagnosed with hydrocephalus after birth. She underwent a ventriculoperitoneal shunt placement surgery at 8 days old to drain excess cerebrospinal fluid from her brain ventricles into her abdomen. The surgery involved placing a catheter from her brain ventricle into her abdomen, with a valve to regulate fluid flow. Precautions were taken due to her young age, including maintaining her body temperature. She was placed under general anesthesia and monitored closely after the surgery for potential complications like infection.
The document describes a medical case report for a 3-day-old female infant admitted to the NICU for neonatal jaundice. She presented with yellowish discoloration of the skin and eyes. Her vital signs were normal except for occasional hypothermia. Her physical exam found jaundice, poor nutrition, and abnormal neurological responses. She was treated and discharged after her jaundice improved over a few days.
This document summarizes information about a 2-year-old male patient named Master Sahitya who was admitted to the hospital for pneumonia. It includes his medical history, physical exam findings, lab results, treatment including antibiotics, and nursing care plan. The patient had a fever, cough and breathing difficulties and was diagnosed with pneumonia likely caused by a previous viral infection. He received antibiotics and other treatments during his hospital stay.
Hydrocephalus is characterized by an abnormal accumulation of cerebrospinal fluid in the brain ventricles. It can be caused by increased CSF production, decreased absorption, or blockage of CSF flow pathways. The document discusses the types, causes, signs and symptoms, diagnostic tests, treatment including shunt surgeries, and nursing management of hydrocephalus.
The nursing care plan addresses a client with schizophrenia and disturbed thought processes. The plan identifies assessments of non-reality based thinking, disorientation, and impaired judgment. Expected outcomes include the client being free from injury, demonstrating decreased anxiety, and responding to reality-based interactions. Interventions include being sincere and honest, setting consistent expectations, not making promises that cannot be kept, and encouraging talking without prying for information to provide structure and avoid reinforcing delusions or mistrust.
This document provides an overview of neurologic nursing lecture notes. It covers:
1. The divisions of the nervous system including the central nervous system (CNS), peripheral nervous system (PNS), and autonomic nervous system (ANS).
2. An overview of the structure and function of the nervous system including the brain, spinal cord, cranial nerves, and spinal nerves.
3. Sympathetic and parasympathetic responses including effects on heart rate, blood pressure, respiration, gastrointestinal function, urinary function and more.
4. Toxic substances that can pass the blood-brain barrier such as bilirubin, lead, ammonia, and carbon monoxide.
Hydrocortisone (brand name Cortef) is a steroid medication used for replacement therapy and treatment of allergic and inflammatory disorders. It works by entering target cells and binding to receptors to initiate anti-inflammatory and immunosuppressive effects. Common side effects include weight gain, increased blood sugar, weakness, osteoporosis and immunosuppression. Nursing considerations for patients on hydrocortisone include assessing for risk factors, monitoring for side effects, and evaluating the effectiveness of treatment.
This document provides information about tuberculous meningitis (TB meningitis). It discusses the anatomy and physiology of the central nervous system and meninges. Key points include:
1) TB meningitis is caused by Mycobacterium tuberculosis infection of the meninges and results in inflammation concentrated at the base of the brain.
2) Symptoms include fever, seizures, headaches, and stiff neck. Diagnosis involves lumbar puncture and analysis of cerebrospinal fluid.
3) Treatment requires a prolonged course of multiple antitubercular drugs as well as steroids to reduce inflammation and potential complications like hydrocephalus.
This document summarizes the development of the central nervous system during the 4th week of gestation. It describes how the neural groove deepens and closes to form the neural tube. Cells within the neural tube then differentiate into neuroblasts and neurons. The meninges develop from surrounding mesenchyme. Vertebral bodies form around the notochord and projections extend around the neural canal to form the vertebral arches. Failure of these arches to fuse can result in spina bifida. The document further describes the types and causes of spina bifida and approaches to management.
Spina bifida is a birth defect where the spine and spinal cord do not form properly. It can range from mild to severe, causing physical and intellectual disabilities. It occurs when the neural tube fails to close fully during early embryonic development. The three main types are spina bifida occulta, meningocele, and myelomeningocele. Treatment involves surgery to repair the spine and prevent infection, along with physical therapy, bladder and bowel management, and orthopedic care. Prevention focuses on adequate folic acid intake before and during pregnancy to help reduce risks.
The family assessment document summarizes a community health nurse's home visit with the Mabatid family. The nurse conducted an initial assessment of the family, collecting information on their structure, socioeconomic factors, environment, and health. Key issues identified were improper waste disposal and a large mosquito presence. The nurse prioritized these problems and created a family nursing care plan focused on educating the family on proper waste segregation and disposal. The activity reinforced the important role community health nurses play in preventive care, health education, and addressing issues at their source within families and communities.
The document provides information on spinal cord injury, including:
- The anatomy and physiology of the spinal cord, including its segments, grey and white matter, and dermatomes and myotomes.
- The classification of spinal cord injuries as complete or incomplete (including types of incomplete injuries like anterior cord syndrome), and types of paralysis.
- The causes, risk factors, signs and symptoms, diagnostic tests, and medical and surgical management of spinal cord injuries.
- Nursing diagnoses and complications related to spinal cord injuries.
This document summarizes several primitive and protective reflexes seen in infants, including the age at which each reflex appears and disappears. It lists 8 primitive reflexes - rooting, sucking, Moro, asymmetric tonic neck, palmar grasp, planter grasp, Babinski, and stepping - along with their descriptions and typical age ranges. It also outlines 4 protective reflexes - neck righting, parachute (sideways), parachute (forward), and parachute (backward) - and notes that they typically persist beyond the listed ages.
The document provides a nursing care plan for a 62-year-old female patient, Mrs. Kulsum, who is being treated for Pott's Spine at L3 and L4 levels. It includes her medical history, physical examination findings, lab results, medications and nursing assessments. The nursing diagnoses identified are acute pain, impaired mobility, altered nutrition, impaired skin integrity, self-care deficit, ineffective coping and risks for infection and aspiration due to her condition and restricted activity.
The patient was experiencing dizziness and had high blood pressure. The nurse assessed the patient and found their blood pressure to be elevated at 180/110. The nurse diagnosed the patient with hypertension and explained to the patient that it is a condition where blood pressure is abnormally high, putting them at risk for health problems like heart disease. The nurse's plan was to educate the patient on hypertension, identify lifestyle factors that could be contributing to it, and ensure the patient understands the importance of following their treatment plan and making healthy changes.
1. The document presents a case study of a 74-year-old male patient diagnosed with Parkinson's disease. It includes details on the patient's history, examination findings, and management.
2. The objectives of the case study were to share knowledge with supervisors, get feedback, and improve presentation skills. Parkinson's disease causes abnormal movements and difficulties with walking.
3. Examination revealed symptoms of Parkinson's disease including a shuffling gait, masked facial expressions, tremors, and rigidity.
Drug study - Tranexamic Acid, Nalbuphine HCL, Ranitidine HCLMj Hernandez
Ceftriaxone sodium is a third generation cephalosporin antibiotic that works by inhibiting bacterial cell wall synthesis, promoting instability and killing bacteria. It is indicated for UTIs, respiratory infections, gynecologic infections, bone/joint infections, intra-abdominal infections, skin infections, and meningitis. Adverse reactions include headache, fever, diarrhea and allergic reactions like rash. Nurses should check for penicillin allergies and monitor patients with impaired vitamin K synthesis or low stores as the drug may affect clotting.
Nalbuphine hydrochloride is an opioid agonist-antagonist used for moderate to severe pain as an adjunct to anesthesia
Dexamethasone is a glucocorticoid that suppresses inflammation and the immune response. It has numerous side effects involving many body systems if used long-term or improperly. It is indicated for chronic inflammatory disorders, allergies, hematologic diseases, neoplasms, and autoimmune diseases. Nursing care for dexamethasone involves frequent monitoring for side effects involving fluid balance, electrolytes, skin, respiratory status, and psychological changes. Patients require education about proper administration and reporting any adverse effects.
The nursing care plan addresses a patient complaining of dizziness. It assesses the patient's risk for hypertension due to lack of disease knowledge. The diagnosis is risk for hypertension. The plan includes defining hypertension and its treatment regimen to the patient, identifying modifiable risk factors like diet and stress, and suggesting lifestyle changes to control blood pressure such as rest, exercise, and limiting sodium and caffeine. The rationale is to educate the patient and decrease risk of end-organ damage from long-term high blood pressure. The evaluation will assess the patient's understanding after interventions.
This nursing care plan addresses impaired skin integrity in a patient. Short term goals within 2 days include the patient reporting any altered sensations or pain at the wound site, understanding the wound healing plan, and describing wound care measures. Long term goals within 2 weeks include decreasing wound size and increased healing tissue. The plan involves assessing the wound characteristics, monitoring for infection signs, providing wound dressing and care, administering antibiotics if needed, educating the patient on nutrition, wound monitoring and care, and repositioning the patient to prevent further injury.
This document provides an overview of magnetic resonance imaging (MRI) and several case examples demonstrating its clinical applications. The key points covered include:
- MRI works by detecting tiny movements of protons in tissue when exposed to magnetic fields. Different sequences like T1 and T2 provide different tissue contrasts.
- Brain MRI is very useful for detecting lesions and assessing anatomy without radiation. Several brain cases demonstrate common conditions like tuberculoma, multiple sclerosis, and mitochondrial disease.
- Spine MRI is now the primary imaging method for evaluating the spine. Examples show common spinal pathologies and the importance of classification of disc abnormalities.
- MRI has many clinical uses beyond the brain and spine, such as cardiac imaging
This document discusses various congenital anomalies that affect the central nervous system, including neural tube defects (NTDs) such as spina bifida occulta, meningocele, meningomyelocele, encephalocele, and anencephaly. It describes the embryology of neural tube formation and risk factors for NTDs such as folic acid deficiency. The document also discusses craniosynostosis, which is the premature fusion of skull sutures, and the various types including plagiocephaly, scaphocephaly, and trigonocephaly. It notes treatment may involve surgery to correct skull growth abnormalities.
A baby girl born at 38 weeks was diagnosed with hydrocephalus after birth. She underwent a ventriculoperitoneal shunt placement surgery at 8 days old to drain excess cerebrospinal fluid from her brain ventricles into her abdomen. The surgery involved placing a catheter from her brain ventricle into her abdomen, with a valve to regulate fluid flow. Precautions were taken due to her young age, including maintaining her body temperature. She was placed under general anesthesia and monitored closely after the surgery for potential complications like infection.
The document describes a medical case report for a 3-day-old female infant admitted to the NICU for neonatal jaundice. She presented with yellowish discoloration of the skin and eyes. Her vital signs were normal except for occasional hypothermia. Her physical exam found jaundice, poor nutrition, and abnormal neurological responses. She was treated and discharged after her jaundice improved over a few days.
This document summarizes information about a 2-year-old male patient named Master Sahitya who was admitted to the hospital for pneumonia. It includes his medical history, physical exam findings, lab results, treatment including antibiotics, and nursing care plan. The patient had a fever, cough and breathing difficulties and was diagnosed with pneumonia likely caused by a previous viral infection. He received antibiotics and other treatments during his hospital stay.
Hydrocephalus is characterized by an abnormal accumulation of cerebrospinal fluid in the brain ventricles. It can be caused by increased CSF production, decreased absorption, or blockage of CSF flow pathways. The document discusses the types, causes, signs and symptoms, diagnostic tests, treatment including shunt surgeries, and nursing management of hydrocephalus.
The nursing care plan addresses a client with schizophrenia and disturbed thought processes. The plan identifies assessments of non-reality based thinking, disorientation, and impaired judgment. Expected outcomes include the client being free from injury, demonstrating decreased anxiety, and responding to reality-based interactions. Interventions include being sincere and honest, setting consistent expectations, not making promises that cannot be kept, and encouraging talking without prying for information to provide structure and avoid reinforcing delusions or mistrust.
This document provides an overview of neurologic nursing lecture notes. It covers:
1. The divisions of the nervous system including the central nervous system (CNS), peripheral nervous system (PNS), and autonomic nervous system (ANS).
2. An overview of the structure and function of the nervous system including the brain, spinal cord, cranial nerves, and spinal nerves.
3. Sympathetic and parasympathetic responses including effects on heart rate, blood pressure, respiration, gastrointestinal function, urinary function and more.
4. Toxic substances that can pass the blood-brain barrier such as bilirubin, lead, ammonia, and carbon monoxide.
Hydrocortisone (brand name Cortef) is a steroid medication used for replacement therapy and treatment of allergic and inflammatory disorders. It works by entering target cells and binding to receptors to initiate anti-inflammatory and immunosuppressive effects. Common side effects include weight gain, increased blood sugar, weakness, osteoporosis and immunosuppression. Nursing considerations for patients on hydrocortisone include assessing for risk factors, monitoring for side effects, and evaluating the effectiveness of treatment.
This document provides information about tuberculous meningitis (TB meningitis). It discusses the anatomy and physiology of the central nervous system and meninges. Key points include:
1) TB meningitis is caused by Mycobacterium tuberculosis infection of the meninges and results in inflammation concentrated at the base of the brain.
2) Symptoms include fever, seizures, headaches, and stiff neck. Diagnosis involves lumbar puncture and analysis of cerebrospinal fluid.
3) Treatment requires a prolonged course of multiple antitubercular drugs as well as steroids to reduce inflammation and potential complications like hydrocephalus.
This document summarizes the development of the central nervous system during the 4th week of gestation. It describes how the neural groove deepens and closes to form the neural tube. Cells within the neural tube then differentiate into neuroblasts and neurons. The meninges develop from surrounding mesenchyme. Vertebral bodies form around the notochord and projections extend around the neural canal to form the vertebral arches. Failure of these arches to fuse can result in spina bifida. The document further describes the types and causes of spina bifida and approaches to management.
Spina bifida is a birth defect where the spine and spinal cord do not form properly. It can range from mild to severe, causing physical and intellectual disabilities. It occurs when the neural tube fails to close fully during early embryonic development. The three main types are spina bifida occulta, meningocele, and myelomeningocele. Treatment involves surgery to repair the spine and prevent infection, along with physical therapy, bladder and bowel management, and orthopedic care. Prevention focuses on adequate folic acid intake before and during pregnancy to help reduce risks.
The family assessment document summarizes a community health nurse's home visit with the Mabatid family. The nurse conducted an initial assessment of the family, collecting information on their structure, socioeconomic factors, environment, and health. Key issues identified were improper waste disposal and a large mosquito presence. The nurse prioritized these problems and created a family nursing care plan focused on educating the family on proper waste segregation and disposal. The activity reinforced the important role community health nurses play in preventive care, health education, and addressing issues at their source within families and communities.
The document provides information on spinal cord injury, including:
- The anatomy and physiology of the spinal cord, including its segments, grey and white matter, and dermatomes and myotomes.
- The classification of spinal cord injuries as complete or incomplete (including types of incomplete injuries like anterior cord syndrome), and types of paralysis.
- The causes, risk factors, signs and symptoms, diagnostic tests, and medical and surgical management of spinal cord injuries.
- Nursing diagnoses and complications related to spinal cord injuries.
This document summarizes several primitive and protective reflexes seen in infants, including the age at which each reflex appears and disappears. It lists 8 primitive reflexes - rooting, sucking, Moro, asymmetric tonic neck, palmar grasp, planter grasp, Babinski, and stepping - along with their descriptions and typical age ranges. It also outlines 4 protective reflexes - neck righting, parachute (sideways), parachute (forward), and parachute (backward) - and notes that they typically persist beyond the listed ages.
The document provides a nursing care plan for a 62-year-old female patient, Mrs. Kulsum, who is being treated for Pott's Spine at L3 and L4 levels. It includes her medical history, physical examination findings, lab results, medications and nursing assessments. The nursing diagnoses identified are acute pain, impaired mobility, altered nutrition, impaired skin integrity, self-care deficit, ineffective coping and risks for infection and aspiration due to her condition and restricted activity.
The patient was experiencing dizziness and had high blood pressure. The nurse assessed the patient and found their blood pressure to be elevated at 180/110. The nurse diagnosed the patient with hypertension and explained to the patient that it is a condition where blood pressure is abnormally high, putting them at risk for health problems like heart disease. The nurse's plan was to educate the patient on hypertension, identify lifestyle factors that could be contributing to it, and ensure the patient understands the importance of following their treatment plan and making healthy changes.
1. The document presents a case study of a 74-year-old male patient diagnosed with Parkinson's disease. It includes details on the patient's history, examination findings, and management.
2. The objectives of the case study were to share knowledge with supervisors, get feedback, and improve presentation skills. Parkinson's disease causes abnormal movements and difficulties with walking.
3. Examination revealed symptoms of Parkinson's disease including a shuffling gait, masked facial expressions, tremors, and rigidity.
Drug study - Tranexamic Acid, Nalbuphine HCL, Ranitidine HCLMj Hernandez
Ceftriaxone sodium is a third generation cephalosporin antibiotic that works by inhibiting bacterial cell wall synthesis, promoting instability and killing bacteria. It is indicated for UTIs, respiratory infections, gynecologic infections, bone/joint infections, intra-abdominal infections, skin infections, and meningitis. Adverse reactions include headache, fever, diarrhea and allergic reactions like rash. Nurses should check for penicillin allergies and monitor patients with impaired vitamin K synthesis or low stores as the drug may affect clotting.
Nalbuphine hydrochloride is an opioid agonist-antagonist used for moderate to severe pain as an adjunct to anesthesia
Dexamethasone is a glucocorticoid that suppresses inflammation and the immune response. It has numerous side effects involving many body systems if used long-term or improperly. It is indicated for chronic inflammatory disorders, allergies, hematologic diseases, neoplasms, and autoimmune diseases. Nursing care for dexamethasone involves frequent monitoring for side effects involving fluid balance, electrolytes, skin, respiratory status, and psychological changes. Patients require education about proper administration and reporting any adverse effects.
The nursing care plan addresses a patient complaining of dizziness. It assesses the patient's risk for hypertension due to lack of disease knowledge. The diagnosis is risk for hypertension. The plan includes defining hypertension and its treatment regimen to the patient, identifying modifiable risk factors like diet and stress, and suggesting lifestyle changes to control blood pressure such as rest, exercise, and limiting sodium and caffeine. The rationale is to educate the patient and decrease risk of end-organ damage from long-term high blood pressure. The evaluation will assess the patient's understanding after interventions.
This nursing care plan addresses impaired skin integrity in a patient. Short term goals within 2 days include the patient reporting any altered sensations or pain at the wound site, understanding the wound healing plan, and describing wound care measures. Long term goals within 2 weeks include decreasing wound size and increased healing tissue. The plan involves assessing the wound characteristics, monitoring for infection signs, providing wound dressing and care, administering antibiotics if needed, educating the patient on nutrition, wound monitoring and care, and repositioning the patient to prevent further injury.
This document provides an overview of magnetic resonance imaging (MRI) and several case examples demonstrating its clinical applications. The key points covered include:
- MRI works by detecting tiny movements of protons in tissue when exposed to magnetic fields. Different sequences like T1 and T2 provide different tissue contrasts.
- Brain MRI is very useful for detecting lesions and assessing anatomy without radiation. Several brain cases demonstrate common conditions like tuberculoma, multiple sclerosis, and mitochondrial disease.
- Spine MRI is now the primary imaging method for evaluating the spine. Examples show common spinal pathologies and the importance of classification of disc abnormalities.
- MRI has many clinical uses beyond the brain and spine, such as cardiac imaging
This document discusses various congenital anomalies that affect the central nervous system, including neural tube defects (NTDs) such as spina bifida occulta, meningocele, meningomyelocele, encephalocele, and anencephaly. It describes the embryology of neural tube formation and risk factors for NTDs such as folic acid deficiency. The document also discusses craniosynostosis, which is the premature fusion of skull sutures, and the various types including plagiocephaly, scaphocephaly, and trigonocephaly. It notes treatment may involve surgery to correct skull growth abnormalities.
Cervical spondylosis syndrome is caused by the degeneration of cervical intervertebral discs and secondary degeneration of cervical joints, which can compress the spinal cord, nerve roots, or vertebral artery. It presents with neck pain and pain or numbness that radiates to the arms. Diagnosis is made through x-rays, CT scans, or MRIs showing osteophyte formation and disc space narrowing. Treatment includes neck braces, physical therapy, medications, and sometimes surgery such as anterior cervical discectomy and fusion. Prevention involves avoiding neck injuries through proper safety techniques.
Floppy infant syndrome is caused by conditions affecting the central nervous system, spinal cord, neuromuscular junction, muscles or peripheral nerves. Key features include generalized hypotonia and weakness, with varying involvement of face, arms and legs depending on the site of involvement. Spinal muscular atrophy is a genetic disorder causing degeneration of motor neurons leading to weakness. Myasthenia gravis is an immune disorder causing weakness through antibodies blocking acetylcholine receptors.
This document provides an overview of the medulla oblongata. It begins with an introduction and outline. It then describes the gross appearance and internal structures of the medulla, including the pyramids, olives, and medial lemnisci. It discusses the blood supply, venous drainage, and functions of the medulla, which include respiration, cardiac and vasomotor centers, and reflex centers. The document concludes by covering diseases of the medulla such as genetic, developmental, vascular, degenerative, infectious, inflammatory, and neoplastic conditions.
The document discusses brain tumors and their classification. It provides details about:
1) Primary brain tumors can arise from neurons, glia or meninges and metastases can spread from other organs. Prognosis depends on histology and location.
2) Brain tumors are classified based on their cell of origin - the majority are neuroepithelial tumors like gliomas and astrocytomas.
3) Symptoms vary based on tumor location but commonly include headaches, seizures, and neurological deficits.
This case describes a patient who suffered a cerebellar infarction after a motorcycle accident without a helmet. Some key points:
- Initial CT was normal but follow up CT showed a large left cerebellar infarction and obstructive hydrocephalus.
- He underwent an emergency suboccipital craniectomy and decompression which allowed for recovery.
- Now, 48 hours later, he is becoming progressively drowsy with vomiting.
My thoughts on what is happening and next steps:
1. He is likely experiencing increased intracranial pressure from edema and hydrocephalus related to the large cerebellar infarction.
2. I would obtain an emergent CT to re-evaluate for worsening
Presentation1.pptx, congenital malformation of the brain.Abdellah Nazeer
More than 2000 congenital brain malformations have been described. Magnetic resonance imaging is useful for studying these conditions. The document provides an overview of important congenital brain malformations, including disorders of organogenesis like Chiari malformations, holoprosencephaly, and cephaloceles. Disorders of histogenesis and cytogenesis such as neurocutaneous syndromes, vascular malformations, and tumors are also discussed. The imaging features of various malformations are presented to aid diagnosis.
CMC Neuroimaging Case Studies - Cerebral Venous Sinus ThrombosisSean M. Fox
Drs. Faith Meyers, Steven Perry, Madison Watts, and Brandon Friedman are Emergency Medicine Residents at Carolinas Medical Center and interested in medical education. Along with the guidance of Dr. Michael Gibbs (Chair of Emergency Medicine), Dr. Jonathan Clemente (Chief of the Department of Radiology and Neuroradiology specialist), Dr. Christa Swisher (Neurocritcal Care Intensivist), and Dr. Scott Wait (Chief of Pediatric Neurosurgery) they aim to help educate us on Neuroimaging. In this presentation they will address Cerebral Venous Sinus Thrombosis. Follow along with the EMGuideWire.com team as they post the CMC Neuroimaging Case Studies.
This set will cover:
- Cerebral Venous Sinus Thrombosis
This document discusses focal cortical dysplasia, a type of neuronal migration disorder caused by abnormal proliferation and migration of neurons during brain development. It begins by providing background on normal cortical development. It then defines focal cortical dysplasia and describes its characteristics and appearance on imaging studies. The document notes that focal cortical dysplasia is a common cause of epilepsy, especially in pediatric patients. Surgical treatment can successfully treat epilepsy in many patients with focal cortical dysplasia if the abnormal cortex is fully resected.
Diagnosis and Management of Special Populations 2010Dominick Maino
Diagnosis and Management of Special Populations presents the latest in the assessment and treatment of those with physical, cognitive, and behavioral abnormalities. Up to date information concerning the etiology, prevalence/incidence and physical/cognitive findings of individuals with developmental/acauired disabilities (Cerebral palsy, Down syndrome, Fragile X syndrome, autism, acquired/traumatic brain injury) will be discussed. New diagnostic and treatment techniques are reviewed. The eye care practitioner will be able to confidently provide eye and vision care for those with disability at the end of this presentation.
1) The document discusses various pathologies that can affect the clivus region, including congenital malformations, acquired conditions, and primary and secondary neoplasms.
2) Examples of discussed pathologies include proatlas segmentation failure, neuroenteric cysts, basilar invagination, fibrous dysplasia, chordoma, plasmacytoma, and meningioma.
3) The pathologies are described in terms of their etiology, clinical presentation, diagnostic evaluation, and treatment options.
This document discusses congenital anomalies of the central nervous system, including their etiology, primary neurulation, neural tube closure, and specific disorders. Key points include: Folic acid deficiency and infections like rubella can cause anomalies. Primary neurulation occurs around 3-4 weeks and involves the neural tube, epidermis, and neural crest. Neural tube closure begins in the cervical region and finishes around day 29. Specific disorders result from failures of these processes and include anencephaly, meningocele, myelomeningocele, encephalocele, and Chiari malformation. Diagnosis involves imaging like MRI and treatment may involve surgical repair or decompression.
The document discusses several types of central nervous system (CNS) tumors including gliomas, meningiomas, and pilocytic astrocytomas. Key points include:
- Gliomas are the most common CNS tumors in adults and children arising from glial cells. Astrocytomas including glioblastoma multiforme are the most common gliomas.
- Meningiomas arise from arachnoid granulation cells and are typically benign, slow growing tumors attached to the dura.
- Pilocytic astrocytomas are a type of low-grade glioma that predominantly affects children and presents as a cystic mass with a mural nodule, often
A 60-year-old female presented with numbness in both lower limbs for 6 weeks and weakness in both lower limbs for 4 weeks. Neurological examination found loss of sensation below the T6 level and impaired vibration and joint position sense. MRI of the dorsal spine showed a lesion in the D4 and D5 vertebral bodies with extradural and intradural components causing spinal cord compression. Differential diagnoses included aggressive hemangioma, plasmacytoma, and aneurysmal bone cyst. Imaging findings were most consistent with aggressive hemangioma.
This OSCE document describes 12 clinical spots or cases presented to a pediatric resident. For each spot, key details are provided such as the patient's history, examination findings, and any relevant investigations. The resident is asked to identify diagnoses, interpretations, treatment plans, and other clinical information. This OSCE evaluates the resident's ability to synthesize clinical data and demonstrate sound medical knowledge and reasoning for various common and important pediatric presentations.
1. Spinal tuberculosis commonly affects the thoracic and lumbar spine in young adults. It can cause neurological deficits through mechanisms such as inflammatory edema, extradural masses, and meningeal involvement.
2. Diagnosis is based on imaging findings on X-ray, CT, or MRI showing bone destruction and abscesses. Treatment involves chemotherapy and sometimes surgery to debride tissue, drain abscesses, or correct deformities.
3. Complications of spinal tuberculosis include paraplegia, cold abscesses, spinal deformities, and recurrence which may require longer treatment or surgical intervention.
This document provides an overview of syringomyelia, including:
- It is a spinal cord cavity filled with cerebrospinal fluid, with a prevalence of 9 per 100,000 people.
- It can be caused by traumatic injury, Chiari malformation, or other craniovertebral junction anomalies.
- Symptoms depend on the location and extent of the syrinx and can include sensory loss, weakness, pain, and autonomic dysfunction.
- Magnetic resonance imaging is the best way to diagnose and assess syringomyelia.
- Treatment may involve surgery to decompress the craniovertebral junction, open the syrinx, or place a shunt
Craniosynostosis is the premature fusion of skull bone sutures, impairing normal brain and skull development. It occurs in 3.4 per 10,000 births, more commonly in males. Types include sagittal, coronal, lambdoid, metopic, and multiple sutures. Diagnosis involves history, examination finding atypical head shape, and radiological confirmation of suture fusion. Treatment is early surgical release of fused sutures and skull reconstruction to allow brain growth. Syndromes like Crouzon and Apert involve additional genetic mutations and systemic abnormalities.
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CP of Spina Bifida
1. By:
Mark Kevin Felisilda, RN
Jun Rey Carlo Fundales,RN
Jonathan Gonzales, RN
Julberry Juan, RN
2. Spina bifida comes from the latin word “divided spine”. is a rare
congenital condition where there is failure of closure of the spinal cord due to
some factors that causes the spinal cord to create a sac-like cyst at the back of
the person. The most common type of this condition is spina bifida occulta. It has
been reported that in 1000 live births 1-2 babies have this kind of condition
worldwide, in the Philippines it has been said that out of 86,241,691² of the
population 5,174 were reported to have spina bifida in the year 2004
(curereaserch.com).
Our patient belongs to the category of spina bifida cystica with
meningocele, a mild and rare form of neural tube defect where the spinal cord is
not involved in the herniation. He was admitted in the neuro female ward with a
chief complain of headache and increase in the head circumference. We chose
this case because this is a rare condition in which it is not commonly seen in the
ward. It is an interesting case because not all have knowledge about this
condition; we want to broaden our knowledge about this case so that we may be
able to help prevent the occurrence of this condition in the community.
3. After two months of exposure at Davao Regional Hospital specifically
at Ortho / Neuro Ward, this case study aims to enhance our knowledge and
understanding regarding the diagnosis of our client so as to develop new skills
in dealing with this kind of illness and to improve our learning regarding Spina
Bifida that would be helpful in our future nursing profession.
After this case study, we will be able to:
• Establish good interpersonal relationship with the client and his family to gain
their cooperation during the process of gathering data;
• Determine the client health status through analyzing the nature of Spina Bifida
and its deviation from the normal physiologic process;
• Trace the health history of the client and his family by taking the past and
present health history to know the predisposing and precipitating factors of
client’s condition;
• Define and discuss thoroughly the complete diagnosis of the client;
4. • Present a through physical assessment on the client’s condition which serves as
a baseline data;
• Discuss the anatomy and physiology of the involved system in the disease;
• Trace the pathophysiology of the disease process by presenting the etiology,
predisposing and precipitating factors, its signs and symptoms present in the
patient;
• Interpret the results of congregated diagnostic procedures and laboratory
examinations and its clinical significance;
• Identify and discuss the different drugs used in the management of the client’s
condition;
• Formulate nursing care plan to provide adequate nursing interventions;
• Make a detailed discharge planning necessary for the wellness of the client
using the acronym METHOD;
• Interpret the general prognosis of the client base on a criteria; and
• Appreciate the experience we had upon accomplishing the said case study as
well as retaining the supplemental knowledge that we were able to acquire
throughout our 2 months exposure on the ward
5. Name: Patient S
Age: 4 years old
Gender: Male
Date of Birth: November 24, 2007
Address: Purok 4, Southern Davao, Panabo City, Davao Del Norte
Religion: Roman Catholic
Nationality: Filipino
Mother’s Name: Sheila
Father’s Name: Arjie
Siblings: Mayumi, Arsheil
Ordinal Position: Second among the three siblings
Ward: Neuro Ward
Date & Time Admitted: January 26, 2012 @ 3:30pm
Admitting Physician: Dr. Lucio Temonio Jr
Chief Complain: Increasing head circumference
Addmitting Diagnosis: Spina Bifida with Non – Communicating Hydrocephalus
Final Diagnosis: Meningocoele T4 – T6 with Syringomyelia T4 – T9, Obstructive
Hydrocephalus Secondary to Chiari II Malformation
6. Mother:
- Visits pre natal check-up
- Complete immunzations
- ( -) medications during pregnancy
- Experienced emesis gravidarum and UTI
- Avoids taking vitamns and supplements
- Sometimes stressed out from work
Patient:
-Cyst growing at the back of the patient
- Advised surgical treatment but refused d/t lack of financial support
- Complete immunizations, no known allergies on food and drugs
- Age 2: experienced convulsion
- Change in behavior: short temper
- Right eye and jaw cannot completely move
- Experience head ache and increase head circumference
-Increasing head circumference and head ache
7. Father’s Side Mother’s Side
Unknown Unknown Mario
Norma
Arjie Arnel † Sheila “Lolong” Unknown
Sheryll
Legend:
Patient S Arsheil - Male
Mayumi
←
- Female
† - Deceased
- Atrio – Septal defect
- Hypertension
- Diabetes
← - Patient
8. - Mesomorphic body built.
- Slightly kyphotic and the right shoulder is lower than the left.
-On DAT with SAP
-IVF of D5.03 Nacl 500cc @ 60cc/hr, infusing well at left metacarpal vein.
Temperature: 36.8°C
Heart Rate: 108 bpm
Pulse Rate: 100 bpm
Respiratory Rate: 25 cpm
Blood Pressure: 90/60 mmHg
9. 1/26/12 The doctor ordered to admit in neuro ward
Insert IVF
For VP shunting
1/27/12 For official reading of CXR
For pedia clearance
1/28/12 Ordered ECG 12 leads
1/29/12 Discontinue IVF
1/30/12 For Cranial CT scan
1/31/12 To secure 1 unit PRBC for OR use
10. 2/1/12 Pre op orders made
For insertion of IVF
Provided with pedia clearance
2/2/12 Post Op orders
Ordered CBC post operative
2/3/12 May have DAT with SAP
Still flat on bed
2/4/12 May elevate head with 1 pillow
11. 2/5/12 For dressing tomorrow
2/6/12 Decrease IVF to 50 cc/hr
D/C Tramadol & Ranitidine
2/7/12 May now remove IVF
Shift IV Meds to P.O
2/8/12 MGH as ordered
12.
13.
14. Predisposing Precipitating factors:
factors: - Nutrition
- Age - Medications
- Heredity - Socio-economic factors
- Unknown -Diabetes
- Increased body temp
1st month of
pregnancy
Central Nervous
System begins to
form
Defect in the spinal
cord
Failure of spine to join Defect in the closure
the lumbosacral area of the neural tube
Dx:
Spina bifida - X ray
occulta - CT scan Protruding sac through Protrusion with some
- MRI the defect- containing parts of the spinal
meninges cord
15. s/sx:
- dimple formation of Meningocele Myelomeningocele
the affected area
- tuft of hair in the
affected area Dx:
-Translumination
- CT scan
- MRI
If Treated If Not
- Surgical repair of
menigocele
No diret flow of csf
and myelomeningocele to the spinal cord
Good Prognosis Obstruction of fluid
in the brain
CSF unable to
circulate
s/sx:
- increased ICP Hydrocephalus
- increase head Accumulation of CSF
circumference in the brain
- sunken eyeballs
- vomiting
16. Fluid may
If Treated If Not possibly force
their way out
-VP shunt Fluid continues
to accumulate in Displacement of
the brain the foramen
magnum
Good Prognosis Shunt
Learning
Complication Chiari malformation
disabilities
s/sx: Mental s/sx:
- headache retardation - headache - muscle weakness
- nausea & vomiting - nausea - increased ICP
- fever - dizziness
If not treated
Myelomeningocele Compression of
the spinal cord
Flaccid paralysis Loss of bowel Loss of sensation s/sx:
of the lower control and bladder choking, arm
limb control stiffness, difficulty in
feeding, swallowing, and
Impaired mobility breathing
Impaired urinary Impaired bowel
elimination elimination
Muscle atrophy
17. Hematology Jan 26, 2012 – CBC, Blood typing Creatinine,Electrolytes Jan 26, 2012
Blood component B+ Creatinine 56.9mmol/L Normal
Hemoglobin 126g/L Decreased Sodium 145.8 mmol/L Normal
WBC 7.4 10^g/L Normal Potassium 3.73 mmol/L Normal
Neutrophils .31 Decreased
Calcium 1.19 mmol/L Normal
Lymphocytes .60 Increased
Eosinophils .09 Increased
Hematocrit .35 Decreased
Protrombine time 14.0 Normal
APTT 34.5 secs Normal
Cranial CTS Jan 31, 2012
Urinalysis Jan 26, 2012 - Non communicating hydrocephalus
- No evident acute intracerebral hemorrhage
Color Light yellow Normal
Leukocytes Negative Normal
Albumin Negative Normal
pH 6.0 Normal
Sugar Negative Normal
Sp. Gravity 1.005 Decreased
Blood Negative Normal
Pus cells 0-2 Normal
18. Hematology Feb 2, 2012 –CBC Feb 5, 2012
Culture and Sensitivity
Hemoglobin 126g/L Decreased
No growth after 72 hours of incubating
WBC 7.4 10^g/L Increased
Neutrophils .31 Increased
Lymphocytes .60 Normal
Hematocrit .35 Decreased
FBS Feb 2, 2012
2.48 mmol/L Normal
CSF analysis Feb 2, 2012
Color Colorles Normal
s
Transpar Cloudy Indicates increase in WBC
ency or infection
Lymphoc 92 Increased
ytes
20. Brand name: Apo-metoclop
Classification: Antiemtic
Mode of Action: Bocks chemoreceptor trigger zone
which prevents or minimize
nausea and vomiting
Indication: Prevent or reduce vomiting during and
after operation
Side Effects:
CNS: sedation, fatigue, headache
GI: dry mouth, constipation, nausea and vomiting,
diarrhea
GU: decrease libido
CV: hypotension, bradycardia
Systemic: rashes
21. Brand name: Suprax
Classification: 3rd Generation Cephalosphorin
Mode of Action: Inhibits cell wall synthesis
Indication: Prophylaxis for post op patients
Side Effects:
CNS: headache, dizziness
GI: nausea and vomiting, diarrhea, abdominal pain
GU: nephrotoxicity
Integ: rash, urticaria
Respi: dyspnea
Systemic: anaphylaxis
22. Brand name: Zinacef
Classification: 2nd Generation Cephalosphorin
Mode of Action: Inhibits cell wall synthesis
Indication: Prophylaxis for post op patients
Side Effects:
CNS: dizziness, headache
GI: diarrhea, nausea and vomiting, abdominal
cramps
GU: nephrotoxicity
Systemic: anaphylaxis
23. Brand name: Paracetamol, Acetaminophen, Tylenol
Classification: Antipyretic, Analgesic
Mode of Action: Block pain impulses peripherally that
occur in response to inhibition of
prostaglandin synthesis; anti pyretic
action results from inhibition of
prostaglandin in the CNS
Side Effects:
CNS: drowsiness
GI: nausea and vomiting, diarrhea, hepatotoxicity
Integ: rash, urticaria
24. Brand Name: Toradol, Tramal, Oltram
Classification: Opioid analgesic
Mode of Action: Not completely known, binds to opioid
receptors, inhibits reuptake of
norepinehrine
Indication: to relieve pain
Side Effects:
CNS: dizziness, headache, anxiety
GI: nausea and vomiting, GI bleeding, constipation
CV: orthostatic hypotension, decrease blood pressure
25. Computation: Rating Scale:
POOR –1 x 2 = 2 0 – 1.5 = Poor
FAIR – 2 x 2 = 4 1.5 – 2.0 = Fair
GOOD – 3 x 3 = 9 2.0 – 2.5 = Good
Total: 15 / 7 = 2 = GOOD
CONCLUSION: