This document discusses a case of a 68-year-old female smoker presenting with malaise and poor appetite. Lab results showed hyponatremia. A CT scan revealed a right lung nodule. The patient was diagnosed with SIADH secondary to the lung mass. The document then provides details on hyponatremia, the approach to evaluating and treating a patient with hyponatremia including the role of arginine vasopressin, SIADH, and treatment strategies such as fluid restriction, demeclocycline, urea, lithium, and the non-peptide vasopressin receptor antagonist tolvaptan. It summarizes results from the SALT trials demonstrating tolv
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
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- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Antimicrobial stewardship to prevent antimicrobial resistanceGovindRankawat1
India is among the nations with the highest burden of bacterial infections.
India is one of the largest consumers of antibiotics worldwide.
India carries one of the largest burdens of drug‑resistant pathogens worldwide.
Highest burden of multidrug‑resistant tuberculosis,
Alarmingly high resistance among Gram‑negative and Gram‑positive bacteria even to newer antimicrobials such as carbapenems.
NDM‑1 ( New Delhi Metallo Beta lactamase 1, an enzyme which inactivates majority of Beta lactam antibiotics including carbapenems) was reported in 2008
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4. Hyponatremia
Hyponatremia defines as serum sodium
concentration <135meq/L.
Most frequent electrolyte abnormality in the
hospitalized pt.
Essentially common in critical care units. In addition
to being a potentially life-threatening condition,
hyponatremia is an independent predictor of death
among intensive care unit and geriatric patients and
those with heart failure, and cirrhosis.
(Arief at al 1976; Terian et al 1994; Borroni et al 2000; Lee et al 2000, Bennani et al 2003;
Goldberg et al 2004: Ruf et la 2005).
5. Hyponatremia
Changes in serum sodium concentration results
from derangements in water balance.
Low serum sodium concentration denotes a
relative deficit of sodium and /or a relative
excess of water.
As seen in the formula, hyponatremia may result
from either a decrease in the numerator or an
increase in the denominator.
Serum sodium = total body sodium
total body water
6. Approach to the patient with
Hyponatremia
Check serum osmolality.
increased or decreased.
Increased osmolality-----
---mannitol, glyceine or hyperglycemia
---movement of water from ICF to ECF
compartment. It causes translocational
hyponatremia.
Decreased osmolality can be due to other
causes.
7. Approach to the pt with
hyponatremia
Decreased serum osmolality --check
volume status. It could be:
Hypovolumeic,
Hypervolumeic or
Euvolumeic.
8. Approach to the patient with
Hyponatremia
Hypovolumeic Hyponatremia
(Dehydartion)
Decrease Sodium
Decrease water
Causes
Diarrhea
Diuretic use
Mineralcorticoid defeciency
Osmotic diuresis like mannitol
9. Approach to the patient with
Hyponatremia
Hypervolumeic Hyponatremia
Sodium content unchanged
Increase water
Causes
Heart Failure
Cirrhosis
Nephrotic syndrome
10. Approach to the patient with
Hyponatremia
Euvolumeic Hyponatremia
Sodium content unchanged
Relative increase in water
Cause
Syndrome of inappropriate diuretic hormone
(SIADH)
11. Approach to the patient with Hyponatremia
Hyponatremia with decreases serum osmolality
ECF volume ECF volume ECF volume
decreased normal (euvolumic) increased (edema)
Renal Extrarenal SIADH CHF
Diuretics GI losses Cirrhosis
Nephrotic syndrome
Urine Na Urine Na Urine Na Urine Na
TB Na
TB water
TB Na
TB water
TB Na
TB water
15. Vasopressin Action
After binding of AVP to V2
receptors --- c-Amp is formed---
increased expression of AQP2 and
AQP3 – insertion into cell
membrane.
Increase driving force for water
reabsorption.
Increased water flow in collecting duct.
16. Collecting duct Cell
Luminal surface Basolateral surface
Aquaporin 3
Aquaporin 4
V2 repceptors fpr ADH
Recycling
vesicles for
AQP-2 ADH
Without
ADH
collecting
duct is
impermeable
to water.
17. Collecting duct cell
Luminal surface
Basolateral surface
Aquaporin 3
Aquaporin 4
V2 repceptors for ADH
AQP-2
ADH
In Presence
of ADH
collecting
duct is
permeable
to water.
18. SIADH
Inappropriate release of ADH causes
siadh.
It is diagnosed by checking :
Serum sodium <135
Serum osmolality <280
Urine osmolality >100
Urine sodium >30
also low serum uric acid <4.0
25. Treatment strategies for Acute
hyponatremic emergencies
3% NaCl: 100ml bolus for severe
symptoms.
3% NaCl@1 to 2ml/kg/hr for 2 to 4 hours
plus furosemide.
Goal: correction by 4 to 6 mEq/L in first
few hours.
Monitor closely to avoid excessive
correction.
26. Treatment strategies for
chronic hyponatremia
Treatment Mechanism Advantages Limitations
Fluid restriction
(0.5- 1 liter/day)
Water intake Effective,
inexpensive
Poor compliance
Demeclocycline
(600-
1200mg/d)
Inhibits action
of adh
Easily available 3-4 days for
onset,
nephrotoxicity
Urea
(30mg/d)
Osmotic
diuresis
Decreased risk Poor
palatability,
Avoid in ckd
Lithium
(up to
900mg/d)
Inhibits action
of adh
Easily available Slow onset,
toxicity
27. Rate of correction
Acute symptomatic :
4 to 6 mEq/L in first 4 hours
Target <12 mEq/L in first 24 hours.
Chronic:
Target correction at <8 mEq/L in first 24 hours
Goal not to exceed;
12 mEq/L in first 24 hr
18 mEq/L in first 48 hr
28. Importance of appropriate serum
sodium correction
Too-rapid correction of hyponatremia (e.g., >12
mEq/L/24 hours) can cause osmotic
demyelination syndrome (ODS) resulting in:
dysarthria, dysphagia,
seizures, coma and death
spastic quadriparesis.
Risk factors for ODS:
severe malnutrition,
alcoholism,
advanced liver disease
29. The ideal therapy
Water excretion without electrolyte excretion
(Na+ and K+) Aquresis.
Prompt but safe correction in 24-48 hours;
<12mEq/L in first 24 hr
< 18mEq/L in first 48 hr
Eliminates fluid restriction.
Predictable and reliable action
Sustained effect and titratable
No unexpected side effects/toxicities.
30. Non-peptide AVP receptor
antagonist (Vaptans)
Aquaretic nonpeptide arginine vasopressin
receptor (AVPR) antagonists are safe and
effective hyponatremia therapies.
Varbalis,JG at al, Hyponatremia treatment guidelines 2007, Am J of
Med, 2007 Nov;120(11 Suppl 1):S1-21
Vaptans lead to aquaresis, an electrolyte-
sparing excretion of free water, that results in
the correction of serum sodium concentration.
Vasopressin antagonists in treatment of hyponatremia; Olszewski,W; Pol Arch MED
Wewn, 2007 Aug:117(8)
31. Non-peptide AVP receptor
antagonist
tolvaptan lixivaptan satavaptan conivaptan
Receptor V2 V2 V2 V1a/V2
Route of
administration oral oral oral IV
Urine volume
Urine osmolality
Na excretion/
24 hours
Low dose
High Dose
32. Non-peptide AVP receptor
antagonist
tolvaptan lixivaptan satavaptan conivaptan
Receptor V2 V2 V2 V1a/V2
Route of
administration oral oral oral IV
Urine volume
Urine osmolality
Na excretion/
24 hours
Low dose
High Dose
Not available in United
states
33. SALT Trial
Multicenter randomized, placebo-controlled,
double-blind phase 3 studies (Study of
Ascending Levels of Tolvaptan in Hyponatremia
1 and 2) [SALT-1 and SALT-2]
225 pts with hyponatremia due to SIADH,
cirrhosis or CHF vs 223 controls.
Serum Na <135 without neurological symptoms.
R.W.Schrier et al; Tolvaptan,a selective oral vasopressin v2 receptor
antagonist, for hyponatremia. New Eng JM, vol 355, no 20.Nov 16,2006
34. SALT Trial
Pt were randomly assigned to placebo vs 15mg
of tolvaptan
Dose of tolvaptan was increased to 30mg and
then to 60mg if necessary.
Primary end points;
Change in serum sodium from baseline to day 4
and day 30.
Serum sodium a week after discontinuation of
drug.
35. SALT Trial
Significant increase in as early as 8 hours :
7% of tolvaptan-treated patients had an increase in
serum sodium greater than 8 mEq/L
vs 1% of placebo-treated patients
Results consistent among patients with
heart failure, cirrhosis, and SIADH
The average rates of serum sodium correction
during the treatment initiation (first 24 hours) were
3.83 mEq/L for SAMSCA (15 mg) and
0.30 mEq/L for placebo
38. Results of SALT
In the SALT trials on Day 4, SAMSCA
increased serum sodium concentration by
4.8 mEq/L vs 0.2 mEq/L for placebo.
On Day 30, SAMSCA increased serum
sodium concentration by 7.4 mEq/L vs
1.5 mEq/L for placebo.
40. SALT Trial
None of the patients in these studies had
evidence of osmotic demyelination
syndrome (ODS) or related neurologic
sequel.
In patients receiving SAMSCA who
develop too-rapid rise in serum sodium,
discontinue or interruption of treatment
with SAMSCA and administration of
hypotonic fluid was considered.
41. Results of SALT
Reduced need for fluid restriction
Fluid restriction during the first 24 hours of
therapy with SAMSCA may increase the
likelihood of overly rapid correction of
serum sodium and should be avoided.
42. Results of SALT
Significant effect on fluid balance
With SAMSCA, urine output is greater than fluid
intake, which results in a net negative fluid balance.
43. Samsca
SAMSCA is indicated for the treatment of
clinically significant hypervolemic and
euvolemic hyponatremia (serum sodium
<125 mEq/L ) in heart failure, cirrhosis,
and SIADH.
It is available in 15mg, 30mg and 60mg
tablets.
44. Samsca
SAMSCA is contraindicated in the
following conditions:
Urgent need to raise serum sodium acutely
Inability of the patient to sense or
appropriately respond to thirst
Hypovolemic hyponatremia
Concomitant use of strong CYP 3A
inhibitors
Anuric patients
45. Samsca
SAMSCA should be initiated and re-
initiated in patients only in a hospital
where serum sodium can be monitored
closely.
Too rapid correction of serum sodium (e.g.,
>12 mEq/L/24 hours) can cause serious
neurologic sequel, including osmotic
demyelination syndrome (ODS).