NEONATAL JAUNDICE IS MOST COMMON CAUSE OF MORBIDITY IN 1ST WEEK OF LIFE IT IS ALSO MOST COMMON CAUSE OF READMISSION AFTER DISCHARGE .THIS BEAUTIFUL SLIDE FOR NNJ.
TORCH, which includes Toxoplasmosis, Other (syphilis, varicella-zoster, parvovirus B19), Rubella, Cytomegalovirus (CMV), and Herpes infections, are some of the most common infections associated with congenital anomalies.
Please find the power point on Phototherapy in jaundice . I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
TORCH, which includes Toxoplasmosis, Other (syphilis, varicella-zoster, parvovirus B19), Rubella, Cytomegalovirus (CMV), and Herpes infections, are some of the most common infections associated with congenital anomalies.
Please find the power point on Phototherapy in jaundice . I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
Intrahepatic Cholestasis of Pregnancy : Dr Sharda Jain & Dr Jyoti Agarwal Lifecare Centre
Intrahepatic Cholestasis of Pregnancy : Dr Sharda Jain & Dr Jyoti Agarwal
Intrahepatic cholestasis of pregnancy (ICP) is characterized by Pruritus and an elevation in serum bile acid concentrations, typically developing in the late second and/or third trimester and rapidly resolving after delivery.
neonatal sepsis is commonest cause of death in neonatal period,but it is preventable by prevention,timely recognition appropriate antibiotics and supportive care.
Intrahepatic Cholestasis of Pregnancy : Dr Sharda Jain & Dr Jyoti Agarwal Lifecare Centre
Intrahepatic Cholestasis of Pregnancy : Dr Sharda Jain & Dr Jyoti Agarwal
Intrahepatic cholestasis of pregnancy (ICP) is characterized by Pruritus and an elevation in serum bile acid concentrations, typically developing in the late second and/or third trimester and rapidly resolving after delivery.
neonatal sepsis is commonest cause of death in neonatal period,but it is preventable by prevention,timely recognition appropriate antibiotics and supportive care.
PNEUMONIA IS MAJOR CAUSE OF MORTALITY IN UNDER 5 YR OF AGE, IN THIS PPT I TRIED TO COVER ALL IMPORTANT FACTOR ABOUT PNEUMONIA, FOLLOW WHO PLAN FOR MANAGEMENT GOD WILL DO REST FOR BETTERMENT OF YOUR PT.
DIARRHOEA IS LEADING CAUSE OF MORTALITY IN INDIA AS WELL AS GLOBALLY .THIS IS NICE PPT BASED ON WHO GUIDELINES,DIARRHOEA IS EASY TO TREAT BUT STILL IT IS IS 2ND MOST COMMON CAUSE OF CHILDHOOD MORTALITY AFTER PNEUMONIA
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
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disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
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the 11 DSM-5 behaviors be present within a 12-month period (mild
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The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
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TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of 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 leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
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. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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2. INTRODUCTION
MOST COMMON MORBIDITY IN 1ST WEEK OF LIFE
OCCUR IN; 60% TERM,80% PRETERM
MOST COMMON CAUSE OF READMIASSON AFTER DISCHARGE
IN NEONATES JAUNDICE VISIBLE SKIN AND EYE >5-7MG/DL
IN ADULT >2MG/DL
MOST CASES JAUNDICE IS BENINGN AND NO INTERVENTION IS
REQUIRED.APPROX 5-10% HAVE SINGIFICANT JAUNDICE REQUIRED
TREATMENT TO LOWER S. BILIRUBIN LEVEL
HIGH LEVEL CARRY RISK OF NEUROLOGICAL IMPAIRMENT SO
REQUIRE T/T TO LOWER DOWN
3. 3 BASIC MECHANISM ;
1. INCREASED PRODUCTION FROM DEGRADATION OF RED CELL
2. DECREASE CLEARENCE BY IMMATURE HEPATIC MECHANISM
3. REABSORBTION BY ENTEROHEPATIC MECHANISM
4.
5.
6. TYPE OF BILIRUBIN
UNCONJUGATED BILIRUBIN CONJUGATED BILIRUBIN
BIND TO ALBUMIN CONJUGATED WITH
GLUCOURONIC ACID
FAT SOLUBLE WATER SOLUBLE
CAN CROSS BBB EXCREATED IN STOOL AND
URINE
TOXIN IN HIGH LEVEL TO BRAIN NOT TOXIC
7. PHYSIOLOGICAL VS PATHOLOGICAL JAUNDICE
PHYSIOLOGICAL IMMATURITY OF NEONATES TO HANDLE
INCREASED BILIRUBIN PRODUCTION,
IN TERM JAUNDICE APPEAR 24-72 HR OF LIFE TSB GOES PEAK
LEVEL 12-15MG/DL @ DAY 3 THAN FALL
IN PT PEAK LEVEL OCCUR ON 3-7 DAYS OF AGE CAN RISE
OVER 15MG/DL THAN FALL CAN TAKE WEEKS
8. PATHOLOGICAL JAUNDICE
PRESENCE OF ONE OR MORE OF FOLLOWING CONDITION
WOULD QUALIFY A NEONATES HAVE PATHOLOGICAL JAUNDICE
1. VISIBLE JAUNDICE ON DAY 1ST OF LIFE( >5)
2. PRESENCE OF JAUNDICE ARM AND LEG ON D2(121-13MG/DL)
3. YELLOW PALM AND SOLE ANYTIME
4. TSB INCREASES >.2MG/DL PER HR YA 5MG/DL IN 24 HR
5. SIGN OF ACUTE BILIRUBIN ENCEPHALOPATHY AND
KERNICTERUS
6. DIRECT BILIRUBIN >1.5-2MG/DL AT ANY TIME
7. CLINICAL JAUNDICE PERSISTINGBEYOND 2WK IN TERM AND 3
WK IN PRETERM
9. CAUSES OF PATHOLOGICAL JAUNDICE
HEMOLYSIS; ABO,RH,MINOR GROUP INCOMPATIBILITY,ENZYME
DEF EG G6PD DEFICIT,AIHA
DECREASED CONJUGATION DUE LIVER ENZYME IMMATURITY
INCREASE ENTEROHEPATIC CIRCULATION SUCH AS LACK OF
ADEQUATE FEEDING THAT INCLUDE INSUFFICIENT
BREASTFEEDING /INFANT NOT FEED DUE TO ILLNESS,GI
OBSTRUCTION
EXTRAVASATED BLOOD ;CEPHALHEMATOMA,EXTENSIVE
BRUISING ETC
10. VISUAL INSPECTION
EXAMINE BABY IN BRIGHT NATURAL LIGHT /ALT IN WHITE
FLUORESCENT LIGHT,WITH NO YELLOW BACKGROUND
NAKED BABY….EXAMINE BLANCHED SKIN AND GUMS AND
SCLERA
NOTE EXTENT OF JAUNDICE (KRAMER S LAW
FACE 5-7MG/DL
CHEST 8-10MG/DL
LOWE ABD AND THIGH 12-15MG/DL
SOLES/PALMS >15MG/DL
11. NEONATES AT HIGHER RISK OF JAUNDICE
<38 WK
PREVIOUS CHILD WITH SIGNIFICANT JAUNDICE
VISIBLE JAUNDICE IN FIRST 24 HR OF LIFE
AGE SPECEFIC TSB LEVEL BEING ABOVE >95TH CENTILE
INADEQUACY OF BREASTFEEDING COMMON CAUSE I.E
BREASTFEEDING JAUNDICE
12. MEASUREMENT OF SERUM BILIRUBIN
1. TRANSCUTANEOUS BILIRUBINOMETRY TcB
CAN USE >35 WEEK OR MORE GESTATION AFTER 24 HR OF
LIFE ,
TcB HAS A GOOD CPRRELATION WITH TSB AT LOWER LEVEL
BUT IT BECOME UNRELIABLE ONCE TSB LEVEL GOES
BEYOND 14MG/DL
2. BIOCHEMICAL ; HIGH PERFORMANCE LIQUED
CHROMATOGRAPHY(HPLC) GOLD STANDARD
TSB ESMITATION BY VANDENBERGH REACTION
3. MICRO METHOD OF TSB ESTIMATION; BASED ON
SPECTROPHOTOMETRY AND ESTIMATE TSB ON MICRO
BLOOD SAMPLE
13.
14. LABORATORY TESTS
1. TOTAL AND DIRECT BILIRUBIN
2. BLOOD GROUP AND RH OF MOTHER AND BABY
3. HEMATOCRIT,RETICULOCYTE COUNT AND PERIPHERAL
SMEAR
4. G6PD ASSAY
5. COOMB TEST
6. SEPTIC SCREEN
7. LFT.TFT
8. TPORCH TITRE
9. LIVER SCAN WHEN CONJUGATED HYPERBILIRUBINEMIA
10.USG OF LIVER AND BILE DUCT IN CHOLESTASIS
15. LABORATORY DIAGNOSIS
LABORATORY FEATURE RH ABO
BLOOD TYPE OF MOTHER RH NEGATIVE O
BLOOD TYPE IN INFANT RH POSITIVE A OR B
ANEMIA MARKED MINIMAL
DCT POSITIVE NEGATIVE
ICT POSITIVE USUALLY POSITIVE
20. PHOTOTHERAPY
MAINSTAY OF TREATING HYPERBINEMIA
BLUE GREEN LIGHT 460-490NM ,BILIRUBIN MOLECULE
ISOMERISE TO HARMLESS FORM
CFL,HALOGEN BULB,HIGH INTENSITY LIGHT EMITTING
DIODE(LED) AND FIBROOPTIC SOURCES.
CFL MOST COMMONLY DUE LOW COST AND EASY AVABIELITY
21. LED HAS ADVANTAGE OF LONG LIFE (50,000 HR) AND CAPABLE OF
DELIVER HIGHER IRRADIANCE THAN CFL LAMPS
EXPOSE MAXIMAL SURFACE AREA OF BABY ( AVOIAD BLOCKING OF
LIGHT BY ANY EQUIPMENT,LARGE DIAPER OR EYE
PATCHES,CAP,HAT ,TAPE
MAKE SURE LIGHT FALL ON BABY PERPENDICULARLY IF THE BABY
IN INCUBATOR
MINIMUM INTERRUPTION OF PT DURING FEEDING SESSION OR
PROCEDURE
KEEP THE DISTANCE BABY AND LIGHT 30-45CM
22. PRINCIPLE OF PHOTOTHERAPY
NATIVE BILIRUBIN (WATER INSOLUBLE)
PHOTO ISOMER OF BILIRUBIN (WATER SOLUBLE) STRUCTURAL ISOMERISM I.E LUMIRUBIN
URINE
2. CONFIGURATIONAL PHOTO ISOMERISM Z..E
3. PHOTO OXIDATION OF BILIRUBIN INTO WATER SOLUBLE AND LESS LIPOPHILIC
COLORLESS FORM OF BILIRUBIN
23. PHOTOTHERAPY TECHNIQUE
• PERFORM HAND WASH
• PLACE BABY NAKED IN CRADLE OR INCUBATOR
• FIX EYE SHADES
• KEEP BABY ATLEAST 45 CM FROM LIGHT
• START PHOTOTHERAPY
• FREQUENT EXTRA FEED 2 HRLY
• TURN BABY AFTER EACH FEED
• TEMP RECORD 2-4 HRLY
• WEIGHT RECORD DAILY
• MONITOR URINE FREQUENTLY
• MONITOR BILIRUBIN LEVEL
24. SE OF PHOTOTHERAPY
1. INCREASED INSENSABLE WATER LOSS
2. LOOSE STOOL
3. SKIN RASH
4. BRONZE BABY SYNDROME
5. HYPERTHERMIA
6. HYPOCALCEMIA
25. MONITORING AND STOPPING PHOTOTHERAPY
MONITOR TEMP OF BABY EVERY 2-4 HR,MEASURE TSB EVERY
12-24HR
DISCONTINUE PT ONCE 2 VALUE 12 HR APART FALL BELOW
CURRENT AGE SPECIFIC CUT OFFS
MONITOR REBOUND BILIRUBIN RISE WITHIN 24 HR AFTER
STOPPING PT
ROLE OF SUNLIGHT
NOT HELP IN TREATMENT
A/W RISK OF SUNBURN AND THEREFORE SHOULD BE AVOIDED
26. EXCHANGE TRANSFUSION
DVET SHOULD BE PERFORM IF TSB LEVEL REACH TO AGE SPECEFIC
CUT-OFF VALUE FOR EXCHANGE TRANSFUSION OR INFANT SHOW
SIGN OF ENCEPHALOPATHY IRRESPECTIVE OF TSB LEVEL
INDICATION @ BIRTH----- CORD TSB IS ≥ 5 OR CORD HB≤ 10G/DL
DONE BY PULL AND PUSH TECHNIQUE VIA UMBILICUS UMBILICAL
CATHETOR
VOLUME OF BLOOD 2X VOLUME OF BLOOD OF BABY 160-180ML/KG
TO PREPARE BLOOD FOR DVET 2/3 OF PRBC AND 1/3 OF
P PLASMA
27.
28. OTHER
IVIG REDUCE HEMOLYSIS SO REDUCE JAUNDICE IN ABO/RH INCMPATABILITY
REDUCE SIGNIFICANTLY NEED OF EXCHANGE TRANSFUSION
NOW IVIG HAS REPLACED EXCHANGE TRANSFUSION AS THE SECOND LINE OF TREATMENT IN INFANT
WITH ISOIMMUNE JAUNDICE
DOSE 1G/KG/DOSE IV
IV HYDRATION; IN SEVERE HYPERBILIRUBINEMIA AND EVIDENCE OF DEHYDRATION EG WT LOSS AN EXTRA
FLUID 50ML/KG N/3 OVER 8 HR DECREASE NEED OF ET
PHENOBARBITAL (LUMINAL)/CLOFIBRATE OR STEROIDS NO PROVEN EVIDENCE OF BENEFIT SO SHOULD
NOT BE EMPLOYED