A preterm newborn developed respiratory distress soon after birth, with signs including grunting and cyanosis. Evaluation found respiratory distress syndrome (RDS). The baby was treated with nasal CPAP, surfactant, and mechanical ventilation. RDS is caused by surfactant deficiency in premature infants, resulting in alveolar collapse and impaired gas exchange. Management includes respiratory support, surfactant replacement therapy, and care to prevent complications.
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
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
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
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
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.
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.
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
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
263778731218 Abortion Clinic /Pills In Harare ,sisternakatoto
263778731218 Abortion Clinic /Pills In Harare ,ABORTION WOMEN’S CLINIC +27730423979 IN women clinic we believe that every woman should be able to make choices in her pregnancy. Our job is to provide compassionate care, safety,affordable and confidential services. That’s why we have won the trust from all generations of women all over the world. we use non surgical method(Abortion pills) to terminate…Dr.LISA +27730423979women Clinic is committed to providing the highest quality of obstetrical and gynecological care to women of all ages. Our dedicated staff aim to treat each patient and her health concerns with compassion and respect.Our dedicated group ABORTION WOMEN’S CLINIC +27730423979 IN women clinic we believe that every woman should be able to make choices in her pregnancy. Our job is to provide compassionate care, safety,affordable and confidential services. That’s why we have won the trust from all generations of women all over the world. we use non surgical method(Abortion pills) to terminate…Dr.LISA +27730423979women Clinic is committed to providing the highest quality of obstetrical and gynecological care to women of all ages. Our dedicated staff aim to treat each patient and her health concerns with compassion and respect.Our dedicated group of receptionists, nurses, and physicians have worked together as a teamof receptionists, nurses, and physicians have worked together as a team wwww.lisywomensclinic.co.za/
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.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
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
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
2. • A 32 weeks preterm baby born to a GDM mother by
LSCS, developed distress, grunting, cyanosis soon after
birth. His SPO2 was 90%, hyperoxia test was positive.
Downe’s score was 7, silverman-anderson score 8.
Urgent CXR was done which showed :
4. Now what next ???
• Baby shifted to NICU and put on warmer. RBS was normal,
other blood samples taken. IV fluids were started, ABG was
done which showed acidosis.
• Baby was put on nasal CPAP, meanwhile survanta was arranged.
• Baby then put on venti, surfactant given at 4 hours of life.
• Now clinically better.
11. Suspect surgical cause
• Obvious malformation
• Scaphoid abdomen
• Frothing
• History of aspiration
12. A progressively increasing O2 requirement to
maintain saturation is also a sensitive indicator
of the severity and progress of distress
>95% Term baby, pulmonary hypertension (PPHN)
88-94% 28-34 weeks preterm
85-92% Below 28 weeks gestational age
Guidelines for monitoring oxygen saturation levels
by pulse oximetry
MJAFI, Vol. 63, No. 3, 2007
GeneralConsiderations
13. Hyperoxia test
test Method result diagnosis
Hyperoxia 100 % fio2 5-10
min
Pao2 increases to
> 100 torr
Pao2 increases by
< 20 torr
Parenchymal
lung disease
PPHN / CCHD
Hyperoxia-
hypervetilation
MV 100 % fio2 &
VR 100-150 / min
Pao2 increases to
> 100 torr
w HV
Pao2 increases
at critical Pco2
No increase in
Pao2 with HV
Parenchymal
lung disease
PPHN
CCHD
21. Respiratory Distress Syndrome (RDS)
• Also known as Hyaline Membrane Disease (HMD)
• Commonest cause of preterm neonatal mortality
• RDS occurs primarily in premature infants; its incidence is
inversely related to gestational age and birth weight
Nelson Textbook of Pediatrics, 18th Ed.
Gestational age Percentages
Less than 28 wks 60-80%
32-36 wks 15-30%
37-39 wk 5%
Term Rare
Resp.Dis.Syn.
22. ETIOLOGYAND PATHOPHYSIOLOGY.
• Surfactant deficiency is the 1O cause of RDS.
• Low levels of surfactant cause high surface tension
• High surface tension makes it hard to expand the alveoli.
• Tendency of affected lungs to become atelectatic at end-expiration
when alveolar pressures are too low to maintain alveoli in
expansion
• Leads to failure to attain an adequate lung inflation and therefore
reduced gaseous exchange
23. • With advancing gestational age, increasing amounts of
phospholipids are synthesized and stored in type II alveolar
cells .
• Wk 20: start of surfactant production and storage. Does not
reach lung surface until later
• Wk 28-32: maximal production of surfactant and appears in
amniotic fluid
• Wk 34-35; mature levels of surfactant in lungs
• Quality : The amounts produced or released may be insufficient
to meet postnatal demands because of immaturity.
• Surfactant inactivating states eg maternal DM may lead to
surfactant of lower quality/ immature
24. • Rare genetic disorders may cause fatal respiratory distress
syndrome eg.
• Abnormalities in surfactant protein B and C genes
• gene responsible for transporting surfactant across membranes
(ABC transporter 3 [ABCA3]) are associated with severe and often
lethal familial respiratory disease
34. Initial Care
• Maintain warmth- cold stress will mimic other causes
of distress
• Monitor blood glucose levels- assure they are normal
• Provide enough oxygen to keep the baby pink
35. Is a Clinical diagnosis: respiratory distress occurring soon after birth.
Pay attention to risk factors! Pulse Oximetry: aim for SPO2 >85%.
ROUTINE!
Full blood count and Cultures to check for sepsis: rem culture only
positive 40-50% of the time!! gastic aspirates/ buffy smears for GBS
Chest radiograph: air bronchogram, reticular/ ground-glass appearance
after 6-12 hrs to full opacity later on.
Blood gases: hypoxia, hypercapnia, acidosis. Signs of RESP FAILURE
determine mgmt eg CPAP vs ventilation etc
Electrolytes, glucose, renal and liver function
Echocardiogram: diagnosing PDA, determine the direction and degree
of shunting, making the diagnosis of pulmonary hypertension and
excluding structural cyanotic heart disease
41. • Avery and Mead in 1959 were the first to demonstrate
that surfactant is deficient in the lungs of infants dying
of HMD
• Fujiwara in 1980 reported the 1st successful clinical
trial of tracheal applications of surfactant in infants
with RDS
• Commercial preparations of surfactant were
subsequently approved by the FDA in the USA in 1989
• Pulmonary Surfactants are phospholipids synthesized
in the type II cells lining the alveoli
42. Prophylactic therapy
Extremely preterm <28 wks
<1000 gm
Not routine in India
Rescue therapy
Any neonate diagnosed to have RDS
Surfactant therapy - Issues
Dose 100mg/kg phospholipid Intra tracheal
43. Types of Surfactant
Natural Surfactants: contain appoproteins SP-B & SP-C
• Curosurf (extract of pig lung mince)
• Survanta (extract of cow lung mince)
• Infasurf (extract of calf lung)
Synthetic Surfactants:do not contain proteins
• Exocerf
• ALEC
• Lucinactant (Surfaxin)
46. Mode of administration of Surfactant
• Dosing may be
divided into 2
alliquots and
adminitered via a
5-Fr catheter
passed in the ET
47. Management
Prevention:
• Tocolytics to inhibit premature labor.
• Antenatal corticosteroid therapy:
► They induce surfactant production and accelerate fetal lung
maturation.
► Are indicated in pregnant women 24-34 weeks' gestation at
high risk of preterm delivery within the next 7 days.
► Optimal benefit begins 24 hrs after initiation of therapy and
lasts seven days.
48. Diagnosis of lung maturity
• Amniotic Fluid Lecithin/Sphingomyelin Ratio
• ≥2 suggests lung maturity.
• ≤1.5 associated with HMD
• Phosphatidyl Glycerol estimation
• More specific than L/S ratio
• Absence is invariably associated with HMD
• Gastric Aspirate Shake Test
• Unreliable if gastric aspirate is contaminated with blood
or meconium
• Serial tests can be done to assess maturity of lungs
during course of disease
Resp.Dis.Syn.
49. Shake test
• Take a test tube
• Mix 0.5 ml gastric aspirate +
0.5 ml absolute alcohol
• Shake for 15 seconds
• Allow to stand 15 minutes for
interpretation of result
50. • NATURAL COURSE
• Usually illness peaks in 3 days, then gradual
improvement
• Improvement is often heralded by spontaneous
diuresis and the ability to oxygenate the infant at
lower inspired oxygen levels or lower ventilator
pressures
• Death may occur esp from day2-3
51. MORTALITY
• Death is rare on the 1st day,
• usually occurs between days 2 and 7
• causes are:
• alveolar air leaks (interstitial emphysema, pneumothorax),
• pulmonary hemorrhage
• Intracranial hemorrhage
• Late mortality from bronchopulmonary dysplasia
54. Meconium Aspiration Syndrome
Definition
MAS is defined as respiratory distress in
an infant born through meconium-
stained amniotic fluid (MSAF) whose
symptoms cannot be otherwise
explained
J Perinatol. 2008 Dec
Mec.Asp.Synd
55. Epidemiology
•Most common cause of respiratory
distress in term and post-term infants.
•MSAF observed in 5-25% of all births out
of which 10% develop MAS.
•One third require ventilator support
•10% develop air leaks
•5-10% of them have a fatal outcome
Mec.Asp.Synd
56. What is meconium?
• The term was coined by Aristotle from the Greek word
“meconium arion” meaning “opium like”
• Consists of gastrointestinal, hepatic and pancreatic secretions,
cellular debris, swallowed amniotic fluid, lanugo, vernix
caseosa and blood
• Appear in the fetal intestines by the 10th week of life gradually
increasing in amount to reach 200gms at birth
Mec.Asp.Synd
57. Cause of MSAF
• The passage of meconium from the fetus into amnion is
prevented by lack of peristalsis(low motilin level) , tonic
contraction of the anal sphincter, terminal cap of viscous
meconium.
• Vagal Stimulation due to in utero hypoxia, acidosis, cord or
head compression cause increased peristalsis and a relaxed
anal sphincter.
• Fetal maturation (post term) causes high motilin level
increased peristalsis
Mec.Asp.Synd
58. Risk factors for MAS
• Post term pregnancy
• Primigravida
• Maternal Anemia
• Chorioamnionitis
• Prolonged Labour
• Fetal Distress
• IUGR
• Maternal Age >30yrs
• Maternal DM
• Maternal heavy cigarette
smoking
• Pre-eclampsia / eclampsia
• Oligohydramnios
• Antepartum Hemorrhage
Mec.Asp.Synd
60. Mechanical obstruction of airways
• With onset of respiration – meconium migrates from central to
peripheral airways.
• Thick particulate and viscous meconium lead to complete or
partial airway obstruction.
• Complete obstruction Atelectasis Ventilation-Perfusion
(V-Q) mismatch
• Partial obstruction Ball-valve – air trapping Obstructive
Emphysema Risk of pneumothorax (15 – 33%)
Mec.Asp.Synd
61. Chemical pneumonitis
• Meconium in the airways initiates an inflammatory reaction
• Meconium inhibits oxidative burst and phagocytosis by
neutrophil increased risk of infection
• Meconium induces production of inflammatory cytokines
Injury of parenchyma and vascular leakage injury similar to
ARDS
Mec.Asp.Synd
62. Surfactant inactivation
• Bilirubin, fatty acid, triglycerides, cholesterol and proteins
present in meconium alter phospholipid structure of surfactant
reduced surfactant function
• Bile has cytotoxic effect on Type II Pneumocytes Reduced
surfactant production.
Mec.Asp.Synd
64. Clinical Features
History
• Maternal risk factors present
• Term or Post term Infants
• Meconium Stained Amniotic fluid (Thick
pea soup/Thin)
• IUGR.
• Many babies are depressed at birth.(in utero
aspiration)
Mec.Asp.Synd
65. Physical examination
• Evidence of postmaturity: peeling skin, long fingernails, and
decreased vernix.
• The vernix, umbilical cord, and nails may be meconium-stained,
depending upon how long the infant has been exposed in
utero.
• In general, nails will become stained after 6 hours and vernix
after 12 to 14 hours of exposure .
• umbilical cord staining (thick-15min, thin-1hour)
Mec.Asp.Synd
68. • Features of respiratory distress within first few hours of birth
• The chest typically appears barrel-shaped, with an increased
anterior-posterior diameter caused by over inflation.
• Auscultation reveals rales and rhonchi -immediately after birth.
• Some patients are asymptomatic at birth and develop
worsening signs of respiratory distress as the meconium moves
from the large airways into the lower tracheobronchial tree.
• In case of massive meconium aspiration, meconium pigments
may be absorbed from lungs excreted in urine. Urine may
appear dark brown in colour.
Mec.Asp.Synd
69. Diagnosis
MAS must be considered in any infant
born through MSAF who develops
symptoms of Respiratory Distress with
typical chest x ray findings
Mec.Asp.Synd
70. Diagnosis
• A chest radiographs is characterized by hyperinflation of the
lung field and coarse nodular opacities due to areas of
atelectasis and consolidation.
• There are coarse irregular patchy infiltrates
• A pneumothorax and pneumomediastinum may be present .
Mec.Asp.Synd
75. Diagnosis
• Arterial blood gas measurements typically show hypoxemia and
hypercarbia.
• Infants with pulmonary hypertension and right-to-left shunting
may have a gradient in oxygenation between preductal and
postductal samples.
• Echocardiogram for evaluation of Persistent Pulmonary
Hypertension.
Mec.Asp.Synd
76. Management
• Prenatal management: Key management lies in prevention during
prenatal period.
• Identification of high risk pregnancies and close monitoring.
Pregnancy that continue past due date, induction as early as 41
weeks may help prevent meconium aspiration.
• If there is sign of fetal distress corrective measure should be
undertaken or infant should be delivered in timely manner.
• Amnioinfusion has no role.
Mec.Asp.Synd
77. Delivery Room Management
Baby delivered through MSAF
Intrapartum Suctioning
Assess the baby after 10-15 sec
Vigorous
• HR > 100/min
• Spontaneous Respiration
• Crying
• Reasonable tone
No intervention
Non Vigorous
• Intubate
• Tracheal Suction
Mec.Asp.Synd
78. • When the infant is not vigorous:
1. Place under radiant warmer but delay
stimulation.
2. Clear airways as quickly as possible.
3. Intubation and then suction directly to the ET
tube. repeat until either ‘‘little meconium
is recovered, or until the baby’s heart rate
indicates that resuscitation must proceed
without delay’’.
4. May also require saline lavage to remove
thick particles.
5. After all meconium is sucked out, ventilate
the baby with bag and mask.
Mec.Asp.Synd
79. Postnatal Management
• Shift to NICU setup with respiratory support facilities available
• Gastric wash with normal saline to reduce gastritis and
aspiration of meconium stained products.
• Close monitoring for Respiratory distress.
• Most infants who develop symptoms will do so in the first 12
hours of life.
Mec.Asp.Synd
80. Management
• Consider CPAP, if FiO2 requirements >0.4; however CPAP
mayaggravate air trapping and must be used cautiously.
• Mechanical ventilation: in severe cases (paCO2 >60 mmHg
orpersistent hypoxemia (paO2 <50 mmHg).
• Correct systemic hypotension (hypovolemia, myocardial
dysfunction).
• Manage PPHN, if present
• Manage seizures or renal problems, if present.
• Surfactant therapy in infants whose clinical status continue
todeteriorate.
82. Transient Tachypnea of Newborn
• Also called Wet Lung Syndrome or Type II Respiratory Distress
Syndrome
• The most common cause of neonatal respiratory distress
constituting more than 40 percent of cases
• 11 per 1,000 live births.
• Represents a milder form of HMD or due to failure of drainage
of alveolar fluids resulting in pulmonary edema decreased
compliance and increased airway resistance Respiratory
Distress
Tran.Tachy.Newborn
83. Risk Factors
• Term or Near Term Babies
• Male Child
• Cesarean Section
• Delayed cord clamping or cord milking
• Macrosomia
• Maternal Sedation
• Large amount of IV Fluids to mother during labor
• Maternal Asthma
• Maternal Diabetes
Tran.Tachy.Newborn
84. Clinical Features
• Tachypnea immediately after birth or within 6hrs after delivery
with mild to moderate respiratory distress.
• These manifestations usually persist for 12-24hrs, but can last
up to 72hrs
• Auscultation usually reveals good air entry with or without
crackles
• Usually maintain good color and are alert.
Tran.Tachy.Newborn
85. • X-Ray Chest
• Hyperinflation of the lungs
• Linear streaking at hila due to dilated lymphatics
• Interlobar Fluid
• Mild Cardiomegaly
• Chest x-ray usually shows evidence of clearing by 12-18 hrs
with complete resolution by 48-72 hrs
Tran.Tachy.Newborn
89. TTN is a clinical diagnosis
of exclusion
Tran.Tachy.Newborn
90. General Management
• Provide an adequate nutrion. Infants with sustained
RR >60 breaths/min should not be fed orally &
should be maintained on gavage feedings for RR 60-
80 breaths/min, and NPO with IV fluids or TPN for
more severe tachypnea
91. Results from slow absorption of
lung fluid
Term born by LSCS/IDM /maternal
asthma
Mild respiratory distress
Peaks at about 36 hours of life
Resolve spontaneously
SUMMARY : Transient Tachypnea of
the Newborn
96. Others
Pneumomediastinum
• It can occur with aggressive ETT insertion, Ryle's feeding tube
insertion, lung disease, MV, or chest surgery (e.g., TEF).
Pneumopericardium
Pneumoperitoneum
Subcutaneous emphysema
Systemic air embolism
100. Management
• Conservative therapy: close observation of the
degree of respiratory distress as well as oxygen
saturation, without any other intervention aiming at
spontaneous resolution and absorption of air.
• Needle aspiration should be done for suspected
cases of pneumothorax with deteriorating general
condition until intercostal tube is inserted.
• Decompression of air leak according to the type
(intercostal tube insertion in case of pneumothorax).