This document presents 4 case studies to discuss barriers to correct diagnosis in neurology. Case 1 describes a woman misdiagnosed with back pain who later presented with spinal epidural abscesses. Case 2 involves a man diagnosed with labyrinthitis who later had a cerebellar infarct. Case 3 is about a woman discharged with headaches who returned with a cerebellar infarct. The document emphasizes considering alternative diagnoses and thorough neurological exams to avoid missed diagnoses.
This study examined the incidence and severity of post-dural puncture headache (PDPH) in 151 patients who underwent spinal anesthesia with a 25-gauge needle for cesarean section. The results found that 21 patients (14%) reported PDPH after the procedure. Most PDPH cases were mild to moderate in severity. Onset of PDPH was typically 1-2 days post-procedure. The study recommends further research with larger sample sizes and higher gauge needles to determine the best preventative measures for reducing the incidence of PDPH following spinal anesthesia.
Childhood demyelinating syndromes
In the past decade, the number of studies related to demyelinating diseases in children has exponentially increased. Demyelinating disease in children may be monophasic or chronic. Typical monophasic disorders in children are acute disseminated encephalomyelitis and clinically isolated syndromes, including optic neuritis and transverse myelitis. However, some cases of acute disseminated encephalomyelitis or clinically isolated syndrome progress to become chronic disorders, including multiple sclerosis and neuromyelitis optica. This review summarizes the current knowledge on monophasic and chronic demyelinating disorders in children, focusing on an approach to diagnosis and management.
This document discusses hiccups (singultus), including classification, epidemiology, pathophysiology, etiology, investigation, and treatment options. Hiccups are involuntary contractions of the diaphragm that can be acute (<48 hours), persistent (48 hours to 1 month), or intractable (>1 month). While often benign, persistent and intractable hiccups may indicate underlying central nervous system, gastrointestinal, or cardiovascular pathology. Treatment involves pharmacological options like baclofen and gabapentin or non-pharmacological approaches.
Dr Trevor Pickersgill - Diagnosing a RelapseMS Trust
1) Diagnosing relapses in multiple sclerosis (MS) patients can be complex, as relapses can mimic other conditions and symptoms are not always clearly MS-related.
2) It is important to properly diagnose relapses to determine the MS disease course, guide treatment decisions, and understand the patient's prognosis.
3) In addition to traditional relapses, atypical presentations must be considered, such as relapses related to MS treatments, infections, neurological conditions mimicking MS, and non-neurological or functional issues. A thorough examination is needed.
Post dural puncture headache is a complication that can occur after a lumbar puncture or spinal anesthesia procedure. It is caused by leakage of cerebrospinal fluid through the puncture site in the dura mater, resulting in a decrease in intracranial pressure. Risk factors include being young, female, having a history of migraines or prior PDPH. Symptoms include frontal or occipital headache that worsens with upright position and improves with lying down. Treatment options range from bed rest, fluids and medications to more definitive treatments like epidural blood patch.
This document discusses disease modification in epilepsy. It presents evidence that seizures can cause neuronal injury through mechanisms like elevated biomarkers, hippocampal sclerosis, and hemicranial asymmetry related to seizure duration. Repeated seizures may lead to epileptogenesis through processes like neuroplastic changes, sprouting, and alterations in neuronal feedback loops. Interventions that can delay or prevent epileptogenesis aim to sufficiently prevent seizures and neuronal injury, improve neuronal recovery, and lower the seizure threshold over time to influence the progression of epilepsy from an early to a chronic phase. The cascade of neuronal injury involves mechanisms like glutamate excitotoxicity, calcium influx, free radicals, and mitochondrial damage, which antiepileptic drugs may act on to modify
My memorable case! AN UNANTICIPATED CARDIAC ARREST & UNUSUAL POST-RESUSCITATI...Prof. Mridul Panditrao
ABSTRACT
A case report of a primigravida, who was admitted with severe pregnancy induced hypertension
(BP 160/122 mmHg) and twin pregnancy, is presented here. Antihypertensive therapy was
initiated. Elective LSCS under general anaesthesia was planned. After the birth of both the babies,
intramyometrial injections of Carboprost and Pitocin were administered. Immediately, she suffered
cardiac arrest. Cardio pulmonary resucitation (CPR) was started and within 3 minutes, she was
successfully resuscitated. The patient initially showed peculiar psychological changes and with
passage of time, certain psycho-behavioural patterns emerged which could be attributed to near
death experiences, as described in this case report.
Guillain-Barré syndrome is an acute autoimmune disorder that causes inflammation of the peripheral nerves. It most commonly develops one to three weeks after a respiratory or gastrointestinal infection. Clinical features include rapidly progressive ascending paralysis, loss of deep tendon reflexes, and possible involvement of cranial nerves or the autonomic nervous system. Diagnosis is based on the clinical features and examination findings. Treatment involves intravenous immunoglobulin or plasma exchange to stop progression. Most patients recover fully but it may take several months and some are left with residual deficits.
This study examined the incidence and severity of post-dural puncture headache (PDPH) in 151 patients who underwent spinal anesthesia with a 25-gauge needle for cesarean section. The results found that 21 patients (14%) reported PDPH after the procedure. Most PDPH cases were mild to moderate in severity. Onset of PDPH was typically 1-2 days post-procedure. The study recommends further research with larger sample sizes and higher gauge needles to determine the best preventative measures for reducing the incidence of PDPH following spinal anesthesia.
Childhood demyelinating syndromes
In the past decade, the number of studies related to demyelinating diseases in children has exponentially increased. Demyelinating disease in children may be monophasic or chronic. Typical monophasic disorders in children are acute disseminated encephalomyelitis and clinically isolated syndromes, including optic neuritis and transverse myelitis. However, some cases of acute disseminated encephalomyelitis or clinically isolated syndrome progress to become chronic disorders, including multiple sclerosis and neuromyelitis optica. This review summarizes the current knowledge on monophasic and chronic demyelinating disorders in children, focusing on an approach to diagnosis and management.
This document discusses hiccups (singultus), including classification, epidemiology, pathophysiology, etiology, investigation, and treatment options. Hiccups are involuntary contractions of the diaphragm that can be acute (<48 hours), persistent (48 hours to 1 month), or intractable (>1 month). While often benign, persistent and intractable hiccups may indicate underlying central nervous system, gastrointestinal, or cardiovascular pathology. Treatment involves pharmacological options like baclofen and gabapentin or non-pharmacological approaches.
Dr Trevor Pickersgill - Diagnosing a RelapseMS Trust
1) Diagnosing relapses in multiple sclerosis (MS) patients can be complex, as relapses can mimic other conditions and symptoms are not always clearly MS-related.
2) It is important to properly diagnose relapses to determine the MS disease course, guide treatment decisions, and understand the patient's prognosis.
3) In addition to traditional relapses, atypical presentations must be considered, such as relapses related to MS treatments, infections, neurological conditions mimicking MS, and non-neurological or functional issues. A thorough examination is needed.
Post dural puncture headache is a complication that can occur after a lumbar puncture or spinal anesthesia procedure. It is caused by leakage of cerebrospinal fluid through the puncture site in the dura mater, resulting in a decrease in intracranial pressure. Risk factors include being young, female, having a history of migraines or prior PDPH. Symptoms include frontal or occipital headache that worsens with upright position and improves with lying down. Treatment options range from bed rest, fluids and medications to more definitive treatments like epidural blood patch.
This document discusses disease modification in epilepsy. It presents evidence that seizures can cause neuronal injury through mechanisms like elevated biomarkers, hippocampal sclerosis, and hemicranial asymmetry related to seizure duration. Repeated seizures may lead to epileptogenesis through processes like neuroplastic changes, sprouting, and alterations in neuronal feedback loops. Interventions that can delay or prevent epileptogenesis aim to sufficiently prevent seizures and neuronal injury, improve neuronal recovery, and lower the seizure threshold over time to influence the progression of epilepsy from an early to a chronic phase. The cascade of neuronal injury involves mechanisms like glutamate excitotoxicity, calcium influx, free radicals, and mitochondrial damage, which antiepileptic drugs may act on to modify
My memorable case! AN UNANTICIPATED CARDIAC ARREST & UNUSUAL POST-RESUSCITATI...Prof. Mridul Panditrao
ABSTRACT
A case report of a primigravida, who was admitted with severe pregnancy induced hypertension
(BP 160/122 mmHg) and twin pregnancy, is presented here. Antihypertensive therapy was
initiated. Elective LSCS under general anaesthesia was planned. After the birth of both the babies,
intramyometrial injections of Carboprost and Pitocin were administered. Immediately, she suffered
cardiac arrest. Cardio pulmonary resucitation (CPR) was started and within 3 minutes, she was
successfully resuscitated. The patient initially showed peculiar psychological changes and with
passage of time, certain psycho-behavioural patterns emerged which could be attributed to near
death experiences, as described in this case report.
Guillain-Barré syndrome is an acute autoimmune disorder that causes inflammation of the peripheral nerves. It most commonly develops one to three weeks after a respiratory or gastrointestinal infection. Clinical features include rapidly progressive ascending paralysis, loss of deep tendon reflexes, and possible involvement of cranial nerves or the autonomic nervous system. Diagnosis is based on the clinical features and examination findings. Treatment involves intravenous immunoglobulin or plasma exchange to stop progression. Most patients recover fully but it may take several months and some are left with residual deficits.
Have you ever tried to sleep in a brightly lit room with tubes and wires attached to you and people periodically talking to you ! moving you ! and touching you !
The document discusses strategies for managing sedation in neuro-ICU patients, including:
1) Titrating sedative and analgesic medications to keep patients calm, alert, and free of pain while being lightly sedated.
2) Using scales like the SAS and RASS to regularly assess sedation levels.
3) Preventing and identifying delirium using tools like the CAM-ICU, given its high prevalence in ICUs and association with poor outcomes.
4) Considering patient factors and medications when choosing a sedation regimen to balance safety, efficacy and risk of delirium.
This document describes the case of a 21-month-old boy who presented to the emergency room with a Glasgow Coma Score of 3 after reportedly falling from a standing position on a kitchen chair. Imaging showed subdural hemorrhage, subarachnoid hemorrhage, hypoxic-ischemic encephalopathy, and retinal hemorrhages. The autopsy later revealed an impact site on the skull and fatal injury to the cervicomedullary junction, as well as traumatic spinal cord injury without radiographic abnormality from T5 to T12. Biomechanical analysis could not rule out nonaccidental injury but found the injuries were also consistent with an accidental fall as described.
After watching this lecture, learners will be able to:
Describe the various etiologies of non-traumatic paralysis
Illustrate the neuro exam for the paralyzed patient
Recognize the signs and symptoms of acute peripheral neuropathies
Explain the treatment of acute peripheral neuropathies
This case report describes a 5-year-old boy with nephrotic syndrome who presented with sudden loss of vision. His blood pressure was elevated and imaging showed abnormalities in the parietal lobe white matter. After his blood pressure was normalized, his vision returned within 48 hours and follow-up imaging showed resolution of the abnormalities, leading to a diagnosis of posterior reversible encephalopathy syndrome (PRES). PRES is characterized by neurological symptoms including visual disturbances that are reversible if blood pressure is controlled. The report discusses the clinical features and imaging findings of PRES.
This document summarizes strategies for improving outcomes in ICU patients receiving sedation, including:
1) Using analgesia-first sedation and targeting light sedation to minimize risks of oversedation like longer duration of mechanical ventilation.
2) Regularly assessing sedation levels and pain to guide treatment. Non-benzodiazepine sedatives like dexmedetomidine may reduce risks of delirium.
3) Daily sedation interruption or awakening trials combined with early mobility can decrease duration of mechanical ventilation and length of stay.
The document discusses the pathophysiology of post-dural puncture headache (PDPHA). There are two main mechanisms proposed for PDPHA - excessive loss of cerebrospinal fluid (CSF) leading to intracranial hypotension and traction on pain-sensitive structures, and loss of CSF causing compensatory intracranial venodilation per the Munro-Kellie doctrine. The rate of CSF leak through the dural puncture can exceed the rate of CSF production, especially with larger gauge needles. Factors like needle size, design, and bevel orientation can affect the amount of CSF lost. Reinserting the stylet may help reposition arachnoid tissue and reduce leaks.
A 31-year-old female presented with a 3-week history of frequent, severe left-sided headaches associated with blurred vision, photophobia, and tearing of the left eye. CT scan revealed a 3 cm hyperdense mass in the midline cerebellum with focal cystic areas, causing hydrocephalus. MRI was performed. She was referred to neurosurgery for further management.
Tardive dyskinesia is a delayed onset movement disorder caused by dopamine receptor-blocking agents. It affects 20-50% of patients treated with neuroleptics long-term and is characterized by involuntary movements, especially of the face. Diagnosis involves ruling out other causes and observing symptoms for at least a month after discontinuing the offending drug. Management focuses on withdrawing the causal medication, though symptoms often persist long-term.
1) The document reports on 5 pediatric patients who had early diffuse cerebral hypodensities on CT scans within 5 hours of well-documented accidental head injuries.
2) All 5 patients presented with severe head injuries and immediate, unremitting coma, rapidly progressing to brain death within 48 hours.
3) This suggests that it is possible, though unusual, to develop CT hypodensities as early as 1 hour after accidental head injury in pediatric patients.
Leigh syndrome is a rare neurodegenerative disease caused by mitochondrial dysfunction from a genetic defect. It is characterized by bilateral brain lesions seen on imaging and variable symptoms. While it typically presents in infancy, it can occasionally present in adulthood. The diagnosis involves identifying characteristic brain lesions. Treatment focuses on nutritional supplementation like biotin and thiamine, as well as managing symptoms, but there is no cure for the underlying genetic condition.
This document discusses targeted temperature management (TTM), previously known as therapeutic hypothermia. It provides background on the mechanisms, history, recommendations and methods for TTM. Key points include that inducing mild hypothermia (32-36°C) for 24 hours after cardiac arrest can reduce neurological injury and improve outcomes. Several methods are described for cooling patients, including surface cooling with blankets/pads and internal cooling via intravenous fluids or catheters. Guidelines recommend TTM for comatose cardiac arrest patients with return of spontaneous circulation.
This document discusses the indications and contraindications for regional anesthesia. It notes that suitability depends on the surgery, surgeon preference, experience level, and patient state. Peripheral nerve blocks have advantages like less immunosuppression and nausea, and can be used for patients who can't tolerate general anesthesia. Risks include local anesthetic toxicity, nerve damage, and block failure. Absolute contraindications for neuraxial blocks are patient refusal, infection, coagulopathy, and increased intracranial pressure. Conditions like aortic stenosis and severe mitral stenosis are relative contraindications. Pre-existing neurological conditions were once thought to absolutely contraindicate neuraxial blocks but one study found no negative outcomes in patients who received these blocks
Chronic pains are highly prevalent conditions that are often linked through metaflammation and lifestyle factors. When pain becomes chronic, it undergoes pathological changes including sensitization of the peripheral and central nervous system. Effective management of chronic pains requires a multimodal approach that addresses both the source of pain and pain control through non-invasive and minimally invasive methods before considering more aggressive options.
Anti-NMDA receptor encephalitis is characterized by psychiatric symptoms, seizures, memory deficits, and autonomic dysfunction. It is caused by autoantibodies against the NMDA receptor. Diagnosis involves detecting antibodies in CSF or blood. Treatment includes immunotherapy like steroids, IVIg, or plasma exchange. With prompt treatment, around 75% of patients recover or have mild deficits, but delayed treatment leads to worse outcomes.
Fever, Friend or Foe? - Paul Young's Talk at SMACCprecordialthump
LITFL's Paul Young looks at the evidence for and against a beneficial role for fever in the critically ill in this whimsical and erudite walk through medical history and science. For audio go here: https://gmep.org/media/14605
Georgetown University Hospital Dept of Medicine Grand Roundsapplebyb
This document discusses Creutzfeldt-Jakob disease (CJD), a rare neurological prion disease. It covers the objectives of understanding diagnosis of CJD and managing patients with CJD. It describes the different etiologies of CJD including genetic, variant, and acquired forms. Diagnosis involves clinical signs, EEG, CSF tests, and MRI imaging. Experimental treatments including quinacrine, pentosan polysulphate, and doxycycline are summarized. Care and management of CJD involves education, communication, and symptom management, with the goals of caring for patients and supporting families during the disease course.
Both cases describe patients presenting with severe unilateral orbital or supraorbital pain, conjunctival injection, tearing, nasal congestion, and mild ptosis. Initial diagnoses of migraine or meningitis were revised after symptoms failed to resolve with treatment. Diagnosis of cluster headache was made based on episodic attacks meeting diagnostic criteria of severe unilateral headache, autonomic symptoms and response to corticosteroids. Cluster headache is often misdiagnosed due to lack of awareness of its clinical features.
A 32-year old female with a history of SLE and rheumatic heart disease presented with shortness of breath, leg swelling, and oliguria. Examination revealed signs of heart and kidney failure. Tests confirmed lupus nephritis and positive autoimmune markers. She was treated with antibiotics, diuretics, and steroids, followed by plasma exchange and renal biopsy showing class II lupus nephritis. She later developed fever and a new heart murmur, and was diagnosed with infective endocarditis treated with antibiotics.
1) 53 year old Native American female with history of osteoarthritis, depression, ADHD presented with altered mental status and psychosis 4 days after hip surgery.
2) On examination, she was agitated and diaphoretic with tremors in lower extremities and hyperreflexia. Labs showed elevated CK consistent with serotonin syndrome.
3) She was diagnosed with likely serotonin syndrome from an interaction between her antidepressants and possible amphetamine or THC use, and was admitted to the ICU.
Daily practice in medicine in general need awareness of critical signs and symptoms that can be the presentation of life threatening and fatal conditions
This document presents a case study of a 44-year-old man diagnosed with spontaneous intracranial hypotension (SIH) secondary to cerebrospinal fluid leaks at C1-C3 and T6-T10. He presented with progressive headache, nausea, vomiting, and intermittent double vision. Imaging showed bilateral subdural hematomas and evidence of subarachnoid hemorrhage. He deteriorated with additional cranial nerve palsies until epidural blood patches were placed, which provided immediate relief and full recovery. SIH is often misdiagnosed but can be identified through characteristic symptoms, lumbar puncture findings and imaging evidence of CSF hypovolemia.
Have you ever tried to sleep in a brightly lit room with tubes and wires attached to you and people periodically talking to you ! moving you ! and touching you !
The document discusses strategies for managing sedation in neuro-ICU patients, including:
1) Titrating sedative and analgesic medications to keep patients calm, alert, and free of pain while being lightly sedated.
2) Using scales like the SAS and RASS to regularly assess sedation levels.
3) Preventing and identifying delirium using tools like the CAM-ICU, given its high prevalence in ICUs and association with poor outcomes.
4) Considering patient factors and medications when choosing a sedation regimen to balance safety, efficacy and risk of delirium.
This document describes the case of a 21-month-old boy who presented to the emergency room with a Glasgow Coma Score of 3 after reportedly falling from a standing position on a kitchen chair. Imaging showed subdural hemorrhage, subarachnoid hemorrhage, hypoxic-ischemic encephalopathy, and retinal hemorrhages. The autopsy later revealed an impact site on the skull and fatal injury to the cervicomedullary junction, as well as traumatic spinal cord injury without radiographic abnormality from T5 to T12. Biomechanical analysis could not rule out nonaccidental injury but found the injuries were also consistent with an accidental fall as described.
After watching this lecture, learners will be able to:
Describe the various etiologies of non-traumatic paralysis
Illustrate the neuro exam for the paralyzed patient
Recognize the signs and symptoms of acute peripheral neuropathies
Explain the treatment of acute peripheral neuropathies
This case report describes a 5-year-old boy with nephrotic syndrome who presented with sudden loss of vision. His blood pressure was elevated and imaging showed abnormalities in the parietal lobe white matter. After his blood pressure was normalized, his vision returned within 48 hours and follow-up imaging showed resolution of the abnormalities, leading to a diagnosis of posterior reversible encephalopathy syndrome (PRES). PRES is characterized by neurological symptoms including visual disturbances that are reversible if blood pressure is controlled. The report discusses the clinical features and imaging findings of PRES.
This document summarizes strategies for improving outcomes in ICU patients receiving sedation, including:
1) Using analgesia-first sedation and targeting light sedation to minimize risks of oversedation like longer duration of mechanical ventilation.
2) Regularly assessing sedation levels and pain to guide treatment. Non-benzodiazepine sedatives like dexmedetomidine may reduce risks of delirium.
3) Daily sedation interruption or awakening trials combined with early mobility can decrease duration of mechanical ventilation and length of stay.
The document discusses the pathophysiology of post-dural puncture headache (PDPHA). There are two main mechanisms proposed for PDPHA - excessive loss of cerebrospinal fluid (CSF) leading to intracranial hypotension and traction on pain-sensitive structures, and loss of CSF causing compensatory intracranial venodilation per the Munro-Kellie doctrine. The rate of CSF leak through the dural puncture can exceed the rate of CSF production, especially with larger gauge needles. Factors like needle size, design, and bevel orientation can affect the amount of CSF lost. Reinserting the stylet may help reposition arachnoid tissue and reduce leaks.
A 31-year-old female presented with a 3-week history of frequent, severe left-sided headaches associated with blurred vision, photophobia, and tearing of the left eye. CT scan revealed a 3 cm hyperdense mass in the midline cerebellum with focal cystic areas, causing hydrocephalus. MRI was performed. She was referred to neurosurgery for further management.
Tardive dyskinesia is a delayed onset movement disorder caused by dopamine receptor-blocking agents. It affects 20-50% of patients treated with neuroleptics long-term and is characterized by involuntary movements, especially of the face. Diagnosis involves ruling out other causes and observing symptoms for at least a month after discontinuing the offending drug. Management focuses on withdrawing the causal medication, though symptoms often persist long-term.
1) The document reports on 5 pediatric patients who had early diffuse cerebral hypodensities on CT scans within 5 hours of well-documented accidental head injuries.
2) All 5 patients presented with severe head injuries and immediate, unremitting coma, rapidly progressing to brain death within 48 hours.
3) This suggests that it is possible, though unusual, to develop CT hypodensities as early as 1 hour after accidental head injury in pediatric patients.
Leigh syndrome is a rare neurodegenerative disease caused by mitochondrial dysfunction from a genetic defect. It is characterized by bilateral brain lesions seen on imaging and variable symptoms. While it typically presents in infancy, it can occasionally present in adulthood. The diagnosis involves identifying characteristic brain lesions. Treatment focuses on nutritional supplementation like biotin and thiamine, as well as managing symptoms, but there is no cure for the underlying genetic condition.
This document discusses targeted temperature management (TTM), previously known as therapeutic hypothermia. It provides background on the mechanisms, history, recommendations and methods for TTM. Key points include that inducing mild hypothermia (32-36°C) for 24 hours after cardiac arrest can reduce neurological injury and improve outcomes. Several methods are described for cooling patients, including surface cooling with blankets/pads and internal cooling via intravenous fluids or catheters. Guidelines recommend TTM for comatose cardiac arrest patients with return of spontaneous circulation.
This document discusses the indications and contraindications for regional anesthesia. It notes that suitability depends on the surgery, surgeon preference, experience level, and patient state. Peripheral nerve blocks have advantages like less immunosuppression and nausea, and can be used for patients who can't tolerate general anesthesia. Risks include local anesthetic toxicity, nerve damage, and block failure. Absolute contraindications for neuraxial blocks are patient refusal, infection, coagulopathy, and increased intracranial pressure. Conditions like aortic stenosis and severe mitral stenosis are relative contraindications. Pre-existing neurological conditions were once thought to absolutely contraindicate neuraxial blocks but one study found no negative outcomes in patients who received these blocks
Chronic pains are highly prevalent conditions that are often linked through metaflammation and lifestyle factors. When pain becomes chronic, it undergoes pathological changes including sensitization of the peripheral and central nervous system. Effective management of chronic pains requires a multimodal approach that addresses both the source of pain and pain control through non-invasive and minimally invasive methods before considering more aggressive options.
Anti-NMDA receptor encephalitis is characterized by psychiatric symptoms, seizures, memory deficits, and autonomic dysfunction. It is caused by autoantibodies against the NMDA receptor. Diagnosis involves detecting antibodies in CSF or blood. Treatment includes immunotherapy like steroids, IVIg, or plasma exchange. With prompt treatment, around 75% of patients recover or have mild deficits, but delayed treatment leads to worse outcomes.
Fever, Friend or Foe? - Paul Young's Talk at SMACCprecordialthump
LITFL's Paul Young looks at the evidence for and against a beneficial role for fever in the critically ill in this whimsical and erudite walk through medical history and science. For audio go here: https://gmep.org/media/14605
Georgetown University Hospital Dept of Medicine Grand Roundsapplebyb
This document discusses Creutzfeldt-Jakob disease (CJD), a rare neurological prion disease. It covers the objectives of understanding diagnosis of CJD and managing patients with CJD. It describes the different etiologies of CJD including genetic, variant, and acquired forms. Diagnosis involves clinical signs, EEG, CSF tests, and MRI imaging. Experimental treatments including quinacrine, pentosan polysulphate, and doxycycline are summarized. Care and management of CJD involves education, communication, and symptom management, with the goals of caring for patients and supporting families during the disease course.
Both cases describe patients presenting with severe unilateral orbital or supraorbital pain, conjunctival injection, tearing, nasal congestion, and mild ptosis. Initial diagnoses of migraine or meningitis were revised after symptoms failed to resolve with treatment. Diagnosis of cluster headache was made based on episodic attacks meeting diagnostic criteria of severe unilateral headache, autonomic symptoms and response to corticosteroids. Cluster headache is often misdiagnosed due to lack of awareness of its clinical features.
A 32-year old female with a history of SLE and rheumatic heart disease presented with shortness of breath, leg swelling, and oliguria. Examination revealed signs of heart and kidney failure. Tests confirmed lupus nephritis and positive autoimmune markers. She was treated with antibiotics, diuretics, and steroids, followed by plasma exchange and renal biopsy showing class II lupus nephritis. She later developed fever and a new heart murmur, and was diagnosed with infective endocarditis treated with antibiotics.
1) 53 year old Native American female with history of osteoarthritis, depression, ADHD presented with altered mental status and psychosis 4 days after hip surgery.
2) On examination, she was agitated and diaphoretic with tremors in lower extremities and hyperreflexia. Labs showed elevated CK consistent with serotonin syndrome.
3) She was diagnosed with likely serotonin syndrome from an interaction between her antidepressants and possible amphetamine or THC use, and was admitted to the ICU.
Daily practice in medicine in general need awareness of critical signs and symptoms that can be the presentation of life threatening and fatal conditions
This document presents a case study of a 44-year-old man diagnosed with spontaneous intracranial hypotension (SIH) secondary to cerebrospinal fluid leaks at C1-C3 and T6-T10. He presented with progressive headache, nausea, vomiting, and intermittent double vision. Imaging showed bilateral subdural hematomas and evidence of subarachnoid hemorrhage. He deteriorated with additional cranial nerve palsies until epidural blood patches were placed, which provided immediate relief and full recovery. SIH is often misdiagnosed but can be identified through characteristic symptoms, lumbar puncture findings and imaging evidence of CSF hypovolemia.
1. CC I have been having terrible chest and arm pain for the p.docxberthacarradice
1. CC: “I have been having terrible chest and arm pain for the past 2 hours and I think I am having a heart attack.”HPI: Mr. Hammond is a 57-year-old African American male who presents to the Emergency Department with a chief complaint of chest pain that radiates down his left arm. He states that he started having pain several hours ago and says the pain “it feels like an elephant is sitting on my chest”. He rates the pain as 8/10. Nothing has made the pain better or worse. He denies any previous episode of chest pain. Denies nausea, dyspnea, or lightheadedness. He was given 0.4 mg nitroglycerine tablet sublingual x 1 which decreased, but not stopped the pain.Lipid panel reveals Total Cholesterol 324 mg/dl, high density lipoprotein (HDL) 31 mg/dl, Low Density Lipoprotein (LDL) 122 mg/dl, Triglycerides 402 mg/dl, Very Low-Density Lipoprotein (VLDL) 54 mg/dlHis diagnosis is an acute inferior wall myocardial infarction.1 of 2 Questions:Why is HDL considered the “good” cholesterol?
QUESTION 2
. CC: “I have been having terrible chest and arm pain for the past 2 hours and I think I am having a heart attack.”HPI: Mr. Hammond is a 57-year-old African American male who presents to the Emergency Department with a chief complaint of chest pain that radiates down his left arm. He states that he started having pain several hours ago and says the pain “it feels like an elephant is sitting on my chest”. He rates the pain as 8/10. Nothing has made the pain better or worse. He denies any previous episode of chest pain. Denies nausea, dyspnea, or lightheadedness. He was given 0.4 mg nitroglycerine tablet sublingual x 1 which decreased, but not stopped the pain.Lipid panel reveals Total Cholesterol 324 mg/dl, high density lipoprotein (HDL) 31 mg/dl, Low Density Lipoprotein (LDL) 122 mg/dl, Triglycerides 402 mg/dl, Very Low-Density Lipoprotein (VLDL) 54 mg/dlHis diagnosis is an acute inferior wall myocardial infarction.2 of 2 Questions:Explain the role inflammation has in the development of atherosclerosis.
QUESTION 3
. A 45-year-old woman with a history of systemic lupus erythematosus (SLE) presents to the Emergency Room (ER) with complaints of sharp retrosternal chest pain that worsens with deep breathing or lying down. She reports a 3-day history of low-grade fever, listlessness and says she feels like she had the flu. Physical exam reveals tachycardia and a pleural friction rub. She was diagnosed with acute pericarditis.
Question:
What does the Advanced Practice Registered Nurse (APRN) recognize as the result of the pleural friction rub?
QUESTION 4.
A 15-year-old adolescent male comes to the clinic with his parents with a chief complaint of fever, nausea, vomiting, poorly localized abdominal pain, arthralgias, and “swollen lymph nodes”. States he has felt “lousy” for a couple weeks. The fevers have been as high as 102 F. His parents thought he had the flu and took him to an Urgent Care Center. He was given Tamiflu® and sent home. He says the Tamiflu.
This document discusses two medical cases presented in the Index of Suspicion column of Pediatrics in Review. Case 1 involves a 17-year-old girl with intermittent right arm swelling and pain over 2 years. After extensive testing, she was diagnosed with complex regional pain syndrome type 1 (CRPS). CRPS is caused by autonomic nervous system disruption and is characterized by severe pain, swelling, and skin changes. Case 2 presents a 7-year-old girl with a tender nodule behind her left ear. Imaging and biopsies confirmed the diagnosis.
Neurologic Emergencies 9-4-09 Jacobi medicine residents.pptDiveshBachoo1
The document describes 8 clinical cases presenting with various neurologic emergencies such as neuroleptic malignant syndrome, serotonin syndrome, carotid artery dissection, spinal epidural abscess, venous sinus thrombosis, myasthenic crisis, and Guillain-Barré syndrome. For each case, the history, exam findings, diagnostic workup, differential diagnosis, and management are discussed. The cases aim to review recognition and treatment of common acute neurological conditions.
Neurologic Emergencies 9-4-09 Jacobi medicine residents.pptDivesh Bachoo
This document presents 9 clinical cases involving various neurologic emergencies:
1. A man found unresponsive with rigidity is diagnosed with neuroleptic malignant syndrome based on elevated CK and the diagnostic triad of fever, altered mental status, and rigidity.
2. A woman withdrawing from an antidepressant exhibits features of serotonin syndrome including agitation and hyperthermia.
3. A woman with carotid artery dissection presents with headache, neck pain, and Horner's syndrome.
4. A man with "top of the basilar" syndrome has oculomotor deficits, behavioral changes, and visual field cuts consistent with a hyperdense basilar artery on CT.
5.
- A 2-year-old boy presented to the emergency department after experiencing a seizure associated with a fever of 104°F. His examination in the emergency department was normal.
- Febrile seizures are relatively common in young children, occurring in 4-8% of children between the ages of 6 months and 6 years. They are generally self-limited and do not require extensive evaluation unless prolonged or focal.
- The diagnosis of a febrile seizure must consider the possibility of central nervous system infection as the underlying cause, though for this patient the examination was normal and he likely experienced a simple febrile seizure.
The document discusses and compares croup and epiglottitis. For the first case, the 2 year old boy presented with noisy breathing, chest retractions, flared nostrils, and a barking cough worse at night, with a history of mild upper respiratory infection for 3 days and a fever of 100.4 degrees F. This is most likely a case of croup. The second case involves a 6 year old boy with high fever for 3 hours, sore throat, drooling, sitting with neck hyperextension, and inspiratory stridor, making epiglottitis the likely diagnosis in this case. Both sections provide details on epidemiology, clinical findings, diagnosis, differential diagnosis, management, complications and
This document summarizes key points about evaluating and managing headaches in the emergency department setting. It discusses distinguishing between primary and secondary headaches, red flags to identify high-risk causes, appropriate use of imaging like CT scans and lumbar punctures, specific conditions like subarachnoid hemorrhage and meningitis, and antibiotic treatment for meningitis. Case examples are also provided to demonstrate history taking, exam, differential diagnosis, and management of headache patients.
Mrs. E.W., a 73-year-old woman, presented with dizziness, clumsiness in her left hand, and unsteadiness over one week. Her symptoms progressed to include speech problems, weakness on her left side, and balance issues. Testing revealed abnormalities in her cerebellum but no acute cause was found. Over several weeks her condition deteriorated further. Additional testing uncovered a small tumor in her right breast. She was ultimately diagnosed with paraneoplastic cerebellar degeneration caused by an underlying primary B-cell lymphoma of the breast.
This is a Unfolding Case StudyPatient DetailsPrint Phase In.docxkenth16
This is a Unfolding Case Study
Patient Details:
Print Phase Info
|
Case Study History
Name:
James, Karen
Age:
57 Years
Gender:
Female
Karen James is a 57-year-old female who was admitted to the medical-surgical unit from her primary care physician’s office for treatment and evaluation of persistent and worsening influenza. She has a past medical history of asthma as well as depression and anxiety.
You are currently working on Phase 1. You have completed Phase 0 of this scenario.
Patient Details:
Print Phase Info
|
Case Study History
Name:
James, Karen
Age:
57 Years
Gender:
Female
Phase
1,
Wednesday
16:00
You have assumed care for Ms. James who is admitted to the medical-surgical unit for rehydration and management of respiratory distress.
Orient yourself to the patient and health record by locating the following pieces of information within the System Assessment Report and Patient Teaching, and type your answers in a Miscellaneous Nursing Note:
1). Run a report on all the System Assessments documented for the patient in the last 24 hours. You will need to go to Patient Charting > System Assessments > Show Saved Charting. What was documented for the respiratory effort? What was auscultated in the Lower Right Posterior lobe of the lungs? What was documented related to tissue perfusion?
2). What was the last documented temperature for Karen?
3). Does Ms. James use any sensory aides?
4) What does she rate her pain?
5) What is her MORSE Fall Risk Score?
Review the client's History and Physical, what indications can you see place this patient at risk for mobility issues or falls?
[LEARNER ACTION: In a misc nursing note identify risks for mobility and falls. Explain her score on the MORSE scale.]
When you are finished with this task, you may click Complete this Phase.
Patient Information
Chief Informant:
Patient
Chief Complaint:
Shortness of breath, productive cough
History of Current Problem:
Patient states she has had 3-week history of influenza. Has now developed a severe cough approximately 3 days ago with shortness of breath. Unable to sleep due to cough, which often causes bronchospasms. Patient also complains of fever, fatigue, and right-sided chest pain. Seen in urgent care 3 days ago and given Z-pack. No improvement in symptoms.
Allergies:
None known
Family History:
Mother died at age of 72 with breast cancer. Father is alive at the age of 79 and has congestive heart failure.
Past Medical History
Previous Illnesses:
Patient has asthma. Also states she gets bronchitis every 1-2 years.
Contagious Diseases:
None
Injuries or Trauma:
None
Surgical History:
Tonsillectomy and adenoidectomy as a child.
Dietary History:
Regular diet. Patient is 5'1" and 140 pounds. Has recently lost 20 pounds on Weight Watchers diet.
Other:
--
Social History:
No smoking, no drugs. Uses alcohol in social situations.
Current Medications:
Tylenol 650 mg PO every 4 hours PRN pain .
Viral infection in the central nervous system (CNS) is a common cause of seizures and epilepsy. Acute symptomatic seizures can occur in the context of almost all types of acute CNS viral infection. Secondary generalized seizures begin in one part of the brain, but then spread to both sides of the brain. In other words, the person first has a focal seizure, followed by a generalized seizure.
This file is designed by Mohammad saleh Moallem
learn to solve several cases in low back painHERRY632019
The patient presents with chronic low back pain following a work injury 5 years ago. On examination, he demonstrates vague tenderness in the lower back and limited flexion and extension. The most likely diagnosis is lumbar muscular strain or sprain. The next step is conservative treatment aimed at reducing pain and restoring function, including physical therapy, medications, and patient education. Further imaging or testing is not needed given the benign physical exam.
This 12-year old girl presents with progressive back pain and weakness. Her neuro exam shows diffuse reduced strength and absent reflexes. LP shows elevated protein. Of the treatment options, IVIg would be most beneficial as it is first-line treatment for Guillain-Barré syndrome, which presents with progressive weakness and albuminocytologic dissociation on LP. Steroids are not effective as monotherapy and the other options do not match the presentation or workup findings.
This patient likely has chronic tension-type headache. The key features are bilateral, pressing quality pain not worsened by activity and no associated nausea, visual changes or neurologic deficits. Stress is a common trigger. Naproxen provides relief indicating an inflammatory component. Preventive options include amitriptyline or tizanidine.
This document provides a summary of clinical syndromes and neurological conditions for medical students. It includes tables comparing upper and lower motor neuron signs. It also provides descriptions of various conditions like herpes simplex encephalitis, Guillain-Barre syndrome, cauda equina syndrome, multiple sclerosis, motor neuron disease, myasthenia gravis, Parkinson's disease, and Bell's palsy. Example cases are presented and the appropriate diagnosis and investigations are discussed for each case. Overall the document serves as a review of key neurology topics for medical students.
Similar to Double Jeopardy: Risk in Neurology (20)
International Cancer Survivors Day is celebrated during June, placing the spotlight not only on cancer survivors, but also their caregivers.
CANSA has compiled a list of tips and guidelines of support:
https://cansa.org.za/who-cares-for-cancer-patients-caregivers/
DECODING THE RISKS - ALCOHOL, TOBACCO & DRUGS.pdfDr Rachana Gujar
Introduction: Substance use education is crucial due to its prevalence and societal impact.
Alcohol Use: Immediate and long-term risks include impaired judgment, health issues, and social consequences.
Tobacco Use: Immediate effects include increased heart rate, while long-term risks encompass cancer and heart disease.
Drug Use: Risks vary depending on the drug type, including health and psychological implications.
Prevention Strategies: Education, healthy coping mechanisms, community support, and policies are vital in preventing substance use.
Harm Reduction Strategies: Safe use practices, medication-assisted treatment, and naloxone availability aim to reduce harm.
Seeking Help for Addiction: Recognizing signs, available treatments, support systems, and resources are essential for recovery.
Personal Stories: Real stories of recovery emphasize hope and resilience.
Interactive Q&A: Engage the audience and encourage discussion.
Conclusion: Recap key points and emphasize the importance of awareness, prevention, and seeking help.
Resources: Provide contact information and links for further support.
MBC Support Group for Black Women – Insights in Genetic Testing.pdfbkling
Christina Spears, breast cancer genetic counselor at the Ohio State University Comprehensive Cancer Center, joined us for the MBC Support Group for Black Women to discuss the importance of genetic testing in communities of color and answer pressing questions.
At Apollo Hospital, Lucknow, U.P., we provide specialized care for children experiencing dehydration and other symptoms. We also offer NICU & PICU Ambulance Facility Services. Consult our expert today for the best pediatric emergency care.
For More Details:
Map: https://cutt.ly/BwCeflYo
Name: Apollo Hospital
Address: Singar Nagar, LDA Colony, Lucknow, Uttar Pradesh 226012
Phone: 08429021957
Opening Hours: 24X7
2024 HIPAA Compliance Training Guide to the Compliance OfficersConference Panel
Join us for a comprehensive 90-minute lesson designed specifically for Compliance Officers and Practice/Business Managers. This 2024 HIPAA Training session will guide you through the critical steps needed to ensure your practice is fully prepared for upcoming audits. Key updates and significant changes under the Omnibus Rule will be covered, along with the latest applicable updates for 2024.
Key Areas Covered:
Texting and Email Communication: Understand the compliance requirements for electronic communication.
Encryption Standards: Learn what is necessary and what is overhyped.
Medical Messaging and Voice Data: Ensure secure handling of sensitive information.
IT Risk Factors: Identify and mitigate risks related to your IT infrastructure.
Why Attend:
Expert Instructor: Brian Tuttle, with over 20 years in Health IT and Compliance Consulting, brings invaluable experience and knowledge, including insights from over 1000 risk assessments and direct dealings with Office of Civil Rights HIPAA auditors.
Actionable Insights: Receive practical advice on preparing for audits and avoiding common mistakes.
Clarity on Compliance: Clear up misconceptions and understand the reality of HIPAA regulations.
Ensure your compliance strategy is up-to-date and effective. Enroll now and be prepared for the 2024 HIPAA audits.
Enroll Now to secure your spot in this crucial training session and ensure your HIPAA compliance is robust and audit-ready.
https://conferencepanel.com/conference/hipaa-training-for-the-compliance-officer-2024-updates
We are one of the top Massage Spa Ajman Our highly skilled, experienced, and certified massage therapists from different corners of the world are committed to serving you with a soothing and relaxing experience. Luxuriate yourself at our spas in Sharjah and Ajman, which are indeed enriched with an ambiance of relaxation and tranquility. We could confidently claim that we are one of the most affordable Spa Ajman and Sharjah as well, where you can book the massage session of your choice for just 99 AED at any time as we are open 24 hours a day, 7 days a week.
Visit : https://massagespaajman.com/
Call : 052 987 1315
Unlocking the Secrets to Safe Patient Handling.pdfLift Ability
Furthermore, the time constraints and workload in healthcare settings can make it challenging for caregivers to prioritise safe patient handling Australia practices, leading to shortcuts and increased risks.
TEST BANK For Accounting Information Systems, 3rd Edition by Vernon Richardso...rightmanforbloodline
TEST BANK For Accounting Information Systems, 3rd Edition by Vernon Richardson, Verified Chapters 1 - 18, Complete Newest Version
TEST BANK For Accounting Information Systems, 3rd Edition by Vernon Richardson, Verified Chapters 1 - 18, Complete Newest Version
TEST BANK For Accounting Information Systems, 3rd Edition by Vernon Richardson, Verified Chapters 1 - 18, Complete Newest Version
Can Allopathy and Homeopathy Be Used Together in India.pdfDharma Homoeopathy
This article explores the potential for combining allopathy and homeopathy in India, examining the benefits, challenges, and the emerging field of integrative medicine.
Hypertension and it's role of physiotherapy in it.Vishal kr Thakur
This particular slides consist of- what is hypertension,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is summary of hypertension -
Hypertension, also known as high blood pressure, is a serious medical condition that occurs when blood pressure in the body's arteries is consistently too high. Blood pressure is the force of blood pushing against the walls of blood vessels as the heart pumps it. Hypertension can increase the risk of heart disease, brain disease, kidney disease, and premature death.
2. 2
Goals
Lay out some cases to spur thought and
discussion.
Talk about barriers to correct diagnosis.
Break down your
own biases.
3. 3
Case #1 – Triage (Day 1)
Patient was a 54-year-old female who presented
to the ED with low back pain.
Nurse evaluation:
Vitals: T 98.8°F (37.1°C); P 102; R 16; 9/10 (no BP)
Chief Complaint: Dull but severe pain from neck to
knees posteriorly. No known recent injury.
Moderate distress. Temp with chills and sweats.
4. 4
Case #1 – Physician HPI
C/O back pain. Hx of chronic back pain, sciatica
and R hip bursitis.
Today pain is different than usual. Usually the
pain is lower back; today all the way from her
shoulder blades down to the back of her legs.
Pain is excruciating. She sees a psychiatrist
and is on several psychiatric medications.
Low-grade fever at home, between 99.5°F
(37.5°C) and 100.9°F (38.3°C). She has been
waking up sweaty at night for several days.
5. 5
Case #1 – PMH
PMH – Negative other than the psychiatric
history as above
Social History – Negative
Review of Systems:
Fever
Sweaty episodes
Weak and tired
Remainder of the ROS is negative
6. 6
Case #1 – Physician PE
Vitals: T 98.7°F (37.1°C); P 105; R 18; BP 117/77
General: Alert and responsive. Not toxic
appearing. Does not appear to be in severe
pain. Rates pain 10/10.
HEENT: Normal
Neck: [no documented exam]
Chest: Clear, no distress, nl breath sounds
Abdomen: Soft, NT; no guarding or rebound
7. 7
Case #1 – PE Continued
Back: Diffuse pain to palpation, mid back, low
back, sciatic grooves, posterior thighs. No
point tenderness. SLR negative.
Gait: Ambulates without difficulty.
Neurologic: [There was no documented
neurologic exam].
8. 8
Case #1 - ED Course
Physician ordered 25mg of promethazine
(Phenergan) and 10 mg morphine.
Patient required a second dose of 10 mg
morphine.
After that, the nurse noted partial relief.
Chem 20 all WNL. WBC 9.3. UA WNL.
No imaging.
9. 9
Case #1 - Disposition
Impression: “Exacerbation of chronic back
pain.”
Discharge Plan: “Patient requested an MRI. I
gave her a Rx for an outpatient MRI of the
lumbar spine. No urgency for this. No evidence
by history, examination or an acute neurologic
problem.”
No follow-up documented. No signature on the
discharge form.
10. 10
Case #1 – Day 3
Patient returned to the same ED after her
lumbar MRI.
Triage: Patient moved from MRI to the ED.
Needs pain relief. Sharp pain in mid and lower
back.
Vitals: T 97°F (36.1°C); P 78; R 18; BP 117/68
11. 11
Case #1 – Physician Evaluation
CC: Low back pain.
HPI: In for MRI today. Very uncomfortable.
Increasing pain in the back “very excruciating.”
Long Hx of back pain with multiple physician
referrals. Apparently was a surgical candidate,
but she declined lumbar disc surgery, opting
for conservative treatment. No loss of bowel or
bladder function. No extremity weakness. No
fever or chills. Ambulatory.
12. 12
Case #1 – Physician Evaluation
ROS: Otherwise negative
Physical Exam:
General: Alert but appears sedated
Extremities: Clear
Back: Tender over lumbar area of her back
Neurologic: DTSRs are grossly intact. There
are no sensory or motor deficits.
13. 13
Case #1 – ED Course
Patient received 2 mg IV hydromorphone
(Dilaudid) and 25 mg Promethazine
(Phenergan).
MRI Report: “Moderate sized central disc
protrusion at L5-S1. Mild annular bulging at
L4-L5. Neurolaminal encroachment at L5-S1.
Foramina and central canal are patent.”
Impression: Exacerbation of chronic back pain.
Discharge Plan: See PMD. Prednisone 60 mg
PO for 5 days. Return for increased pain.
14. 14
Case #1 – Day 8
Patient presented to the same ED for a third
time.
Chief Complaint: Low back pain.
HPI: In ED twice; seen by PMD, who ordered
pain meds. Ongoing pain, L4-L5 herniation on
MRI. Has appointment with neurology, but in to
much pain. Requesting admission.
Disposition: Admitted.
15. 15
Case #1 - Inpatient
Orthopedic consultation on day 10; same focus
as prior evaluations. Focus on prior low back
problem.
On day 11 she spiked a temp.
Day 12 ID Consult: Two-week history of shaking
chills and burning sensation down her legs.
Fever yesterday. Culture growing MRSA.
Profound weakness in all four extremities.
Back pain gone, as she has no feeling in her
back or lower extremities.
16. 16
Case #1 – Impression / Outcome
Impression: Bacteremia and spinal epidural
abscess.
Surgical Report: Epidural abscess C6-7
and L5-S1. Purulent material
found at both places.
Patient Outcome: Complete
permanent paralysis in her
lower extremities.
17. 17
Epidural Abscess
Symptoms can involve multiple levels.
Symptoms can move from one level to another.
Fever may be subtle and come and go.
Early there is absence of other neurologic
findings.
No longer only IVDA patients.
18. 18
Epidural Abscess
Plain imaging shows nothing.
Early labs may show nothing.
MRI needs contrast.
MRI may simply miss
the level.
19. 19
Epidural Abscess
Consider epidural abscess in the diff dx:
Change in character of the pain
History of fever or shaking chills
New symptoms with no mechanism!!
Avoid cognitive biases.
Document a complete exam of the relevant
organ system.
21. 21
Case #2 - Triage
A 33-year-old male presented to the ED with
a sudden onset of dizziness.
Triage: Sudden onset of dizziness. Spinning
feeling, vertigo. Started 3 hours PTA. No prior
similar problems.
Hx: HTN
Vitals: T 99.6°F (37.5°C); P 72; R 16; BP 140/90
22. 22
Case #2 – Physician Evaluation
HPI: Sudden onset of dizziness, spinning
feeling. Patient feels like he is off balance and
like he is going to pass out. Has had severe
nausea. No ear pain. No upper resp symptoms.
No headache or weakness.
PMH: HTN
PSH: Neg
Social Hx: Neg
23. 23
Case #2
HEENT: Normal ear exam.
Neck: Supple, no meningeal signs
Chest: Clear, nl BS, no respiratory distress
Heart: S1, S2 Nl, no murmurs
Abdomen: Benign
Extremities: Normal
Neurologic: Cranial nerves 2-12 intact. No
motor or sensory deficits. Reflexes normal.
24. 24
Case #2
Impression: Acute labyrinthitis
Disposition: Home, follow up as needed.
Outcome: He returned to the same ED the following
day with a headache, dizziness, vomiting, and
inability to gaze to the right. CT revealed a right
cerebellar infarct.
Admitted. Later that evening he developed
decorticate posturing. He continued to deteriorate
and died.
The family sued for failure to diagnose during the
first visit. Settled for an undisclosed amount.
25. 25
Case #3
Patient was a 42-year-old female who
presented to the ED with a headache.
Triage:
Headache for one week
Fiorinal Rx for headaches
Vitals: T 98.4°F (36.9°C); P 80; R 12; BP 150/90
26. 26
Case #3 – Physician Evaluation
HPI – Severe headache for 2 weeks. In bed
most of that time. Problem with walking; states
she loses her balance. Headache is severe; not
the worst headache of her life. Denies
associated symptoms.
PMH – Negative
PSH – Negative
Social - Negative
27. 27
Case #3
Constitutional: Awake, alert, O X 3. Appears
uncomfortable
HEENT: Nl TMs, oropharynx. No sinus pain or
pressure.
Neck: Supple, no meningeal signs
Chest: Clear, no rales or rhonchi. No resp
distress
Heart: S1, S2 normal, no murmurs
28. 28
Case #3
Abdomen: Normal exam, including BS, no
tenderness, no distention.
Extremities: All normal.
Neurologic: No focal deficits. CN NL. Motor
and sensory normal.
29. 29
Case #3 – ED Course
Toradol 60 IM
Only lab abnormality was a WBC of 17K,
no shift
CT read as negative by the radiologist
EP performed an LP. All WNL.
Repeat BP was 150/90. The nurse said patient
was C/O neck pain.
Nursing notes indicate pain relieved post-
Toradol.
30. 30
Case #3 - Disposition
Impression: Headache
Discharged to home.
Meds: Lortab and Pen V-K.
Told to follow up with neurologist and return
to the ED if condition worsened.
31. 31
Case #3 – Bounceback
Returned 12 hours later C/O a headache and
dizziness.
Seen by the same ED physician, who noted the
patient had the same complaint but now also
had a sore throat.
Nurse noted BP of 170/104, headache,
dizziness, nausea and pain in the neck.
32. 32
Case #3 – ED Course
Repeat CT with contrast revealed a left
cerebellar non-hemorrhagic infarct that was
new and C/W the CT from the day before.
MRI/MRA revealed left vertebral artery
occlusion with severe stenosis.
After admission, patient became unresponsive.
Intubated and resuscitated.
Massive cerebellar infarct.
Severe permanent disability.
33. 33
Challenges to Correct Diagnosis
Posterior Circulation Stroke
Notoriously challenging to diagnose.
They mimic other conditions.
Neurologic exam can be nuanced in these cases.
Basilar occlusion syndromes present with
hypertonicity that can be spastic and mimic seizure.
Time course is critical.
History often does not direct you to the diagnosis.
High index of suspicion in “bizarre” neurologic
presentations with any focal motor or ocular findings.
34. 34
Questions to Address
in a Case Like This
What was the last known normal time?
This is the time when the clock starts for the
therapeutic window.
Why the consideration of acute
decompensation from meningitis?
If one considers that likely, is LP still reasonable
with the risk of acute intracranial hypertension?
Is there another neurologic diagnosis more
likely than stroke in this case?
35. 35
High-Risk Stroke
Vertebrobasilar Stroke:
Untreated mortality 70%-80%
Survivors moderately to
severely disabled.,
70% recanalized
mortality to 25%-45%
2/3 with favorable outcome
Treatment window probably
up to 12 hours
ENDOSTROKE Study (2015)
tPA is standard of care
Thrombectomy may be helpful
36. 36
Case #4: “My Head Hurts”
26 y/o honorably discharged Marine
She presents to ED with worsening cephalgia
3 months after leaving the service; pain 9/10.
Seen in ED 2 days prior for headache:
Non-focal exam, improved with Toradol
No imaging done, clinical exam only
Discharged home with “migraine” as diagnosis
ROS:
Unremarkable; family notes heavy exercising
Meds:
None reported
37. 37
Case #4
T 99.4°F (37.4°C); P 94; R 22; BP 150/84; 98%
room air; glucose 160
In ED has “non-focal neurologic” examination:
No photophobia / phonophobia
Fundoscopy challenging
Headache seems worse when supine
Symptomatic treatment in ED:
Toradol, Compazine, IVF
Non-con head CT and screening labs
40. 40
Case #4 - ED Course
ED Course:
Some improvement with
medications; pain 4/10
Suddenly complains of
worsening pain
Brief seizure, 60 seconds, tonic-clonic
Post-ictal with left arm weakness
Emergent repeat non-contrast head CT
42. 42
Case #4 - Diagnosis & Treatment
Acute hemorrhagic stroke (ICH)
BP control in ED (SBP < 160)
Coagulation parameters checked and normal
Admitted to Neuro-ICU
Consultation in ED with neurology and
neurosurgery
43. 43
Case #4 - Diagnosis & Treatment
Diagnosis made in ICU
Cerebral venous sinus thrombosis
(Right transverse sinus)
Confirmed on CT – venography and MRI
ICU treatment
Heparin infusion, close monitoring
Good recovery, outstanding outcome
44. 44
Cerebral Venous Vein Thrombosis
Points to consider in this high-risk case:
26 y/o female with no history of migraine
and 2 visits to ED for headache.
Heavy exercise predisposes to dehydration.
NuvaRing / IUD not often reported as a medication.
CVST is notoriously challenging to diagnosis.
Supine positioning that worsens headache is
worrisome for increased intracranial pressure.
Initial non-con head CT on second visit was NOT
normal.
High index of suspicion is necessary.
Journal of Emergency Medicine, Vol. 42, No. 4, pp. 413-416, 2012.
45. 45
Potential ED Pitfalls
Anchoring on migraine
without a prior history.
Failure to recognize CVST in
differential diagnosis.
Average number of visits to an ED to diagnosis
CVST is ≥ 3.
Unusual diagnosis in ED, but potentially lethal.
Failure to recognize CVST may lead to
anchoring
bias by admitting services as well.
Journal of Emergency Medicine, Vol. 28, No. 2, pp. 140-147, 2010.
46. 46
Summary
Stay curious and pay attention to detail.
COMPLETE Neuro exam.
Look for what doesn’t fit.
Its okay to get an MRI.
Walk the patient around before you send
them home.