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Pediatric Growth and Development Guide

The document outlines key aspects of pediatric nursing, focusing on growth and development milestones from neonates to adolescents, including essential nutrients like calcium and vitamin D for absorption. It describes developmental tasks, reflexes, and the importance of vaccinations, while also addressing abnormal heart defects and hematologic disorders such as hemophilia. Additionally, it emphasizes the significance of proper nutrition and monitoring for developmental delays in children.

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0% found this document useful (0 votes)
16 views8 pages

Pediatric Growth and Development Guide

The document outlines key aspects of pediatric nursing, focusing on growth and development milestones from neonates to adolescents, including essential nutrients like calcium and vitamin D for absorption. It describes developmental tasks, reflexes, and the importance of vaccinations, while also addressing abnormal heart defects and hematologic disorders such as hemophilia. Additionally, it emphasizes the significance of proper nutrition and monitoring for developmental delays in children.

Uploaded by

aisajumlail
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

PEDIATRIC NURSING (NORMAL) - essential nutrient needed: CALCIUM

- vitamin required for better absorption: VITAMIN D "Calciferol"


Neonate/Newborn
- normal height for newborn: 20 inches

- height multiplies at:
Infant (Below 1 y.o.)
o 4 years old - 2x

o 12 years old - 3x
Toddler (1-3 y.o.)
DEVELOPMENT

- qualitative changes; observable data
Preschooler (3-6 y.o.) Early Childhood
- developmental tasks: set of skills and competence that
↓ children must accomplish to deal effectively with their
environment.
School Age (6-12 y.o.) Middle Childhood
I. DDST (Denver Developmental Screening Test) – A tool used to
↓ determine delayed, normal, and advanced development

Adolescent (12-18 y.o.)


II. CATEGORIES OF DEVELOPMENT

1. Gross (Big) and Fine (Small) Motor Skills


DEFINITION OF TERMS
- NOTE: gross > fine * (gross skills develop first!)
Growth - increase in size; height and weight.
2. Language
Development - advancement from lower to more advance stage;
skills and abilities; standing and sitting. - universal language of children: crying

Maturation - increase in competence and adaptability; - absent crying: hearing loss.


capabilities, rationalizing.
3. Personal - personality development

- Psychosexual: Sigmund Freud


GROWTH AND DEVELOPMENT
- Psychosocial: Erik Erikson
- have a predictable pattern; continuous, orderly, and
progressive - Cognitive: Jean Piaget

- each human being accomplished these in a manner unique - Moral: Lawrence Kohlberg
to that individual
4. Social
- cephalocaudal (head to tail) *
- PLAY: major socializing event: provides stimulation
- proximodistal (near to far) - e.g. elbows should work first needed to learn.
before the wrist. *
- TYPES OF PLAY:

o Solitary - play alone (infant)


GROWTH
o Parallel - play independently but among other
- quantitative change, measurable data children (toddler)

- rapid during INFANCY * o Cooperative/Associative - children play


together (preschooler)
- slow during SCHOOL AGE
o Competitive - play that involves competition
- increased during the beginning of ADOLESCENCE (school age)

- off during early ADULTHOOD REFLEXES

1. Rooting - stroke the check = starts sucking

I. Weight 2. Sucking - stroke the lips = starts sucking

• one of the most important health indicators! 3. Tonic Neck Reflex - if the child's head faces right, the right arm
will extend and the left arm will flex.
• "at birth, weight is more variable than height."
4. Palmar Grasp - close the fingers around an object.
• normal weight for newborn: 7-7.5 lbs (3.2-3.4 kg)
5. Plantar Grasp - toes curl down when the sole of the foot is
• NOTE: neonatal weight loss is normal IF below 1 lb.
pressed.
• weight multiplies at:
6. Pincer Grasp - holds a small object using the thumb and the
o 6 months - 2x index finger.

o 12 months - 3x 7. Parachute Grasp - extend arms when about to fall.

o 24 months - 4x 8. Babinski Reflex - stroke the sole of the foot = fanning out of the
toes. NOTE: should disappear in toddler stage, if not, may indicate
(+) neurologic disorder (Brain Tumor: "Glioma")
II. Height
9. Moro – Startle Reflex – Moro: Causes by movement/Motion.
- increase due to skeletal growth; elongation of: DIAPHYSIS Startle: Causes by sounds. Most involuntary reflexes start to fade
(middle part of bone) at 6 months
DEVELOPMENTAL MILESTONES C. Signs of Teething

1 Month - drooling

- (+) strong head lag - gum rubbing

- hands predominantly closed - increase thumb sucking

- strong palmar grasp - biting on hard objects

- watched parent's face intently as they talk to the infant - inflammation due to pain (intervention: cold teething
ring)
2 Months
7 Months
- lifts head while in prone (45°)
- sits leaning forward on both hands; sits with support
- closure of posterior fontanelle (TRIANGULAR)
- transfers object from one hand to another
- fading of grasp reflex
8 Months
- demonstrates social smile
- sits steadily unsupported
3 Months
- crawling: stuck in bed/floor
- lifts head while in prone (90º)
- onset of: SEPARATION ANXIETY
- slight head lag
- combines syllables such as "dada" without meaning
- able to hold head more erect when sitting but still bobs
forward - parachute reflex

- (-) grasp reflex 9 Months

- can recognize familiar faces and objects, such as - creeping: not stuck anymore
feeding bottles.
- eruption of lateral incisors
4 Months
- pulls self to standing position and stands while holding on
- rolls from back to side a furniture

- balances head well in sitting position - NOTE: an infant who does not pull to a standing position
by 11 or 12 months of age should be evaluated for
- disappearance of Moro, Tonic, Neck and Rooting Reflex possibility of Developmental Hip Dysplasia

5 Months - Pincer grasp; PRIORITY: prevent aspiration

- can turn from abdomen to back (roll over) 10 Months

- PRIORITY: safety - stand with support

- do not let the infant sleep in prone: may cause SIDS - eruption of lower lateral incisors
(other causes: co-sleeping and soft beddings: can
cause respi. depression) - says "dada" with meaning

- holds head more erect when sitting - develops object permanence

- puts feet to mouth when in supine 11 months

- smiles at mirror image - Cruising: walks while holding on furniture

6 Months XII. 12 Months

- holds bottle - walks with one hand held

- extends arms out to be picked up - may attempt to stand alone and take first step

- begins to imitate sounds - can say 3-5 words with meaning

- onset of STRANGER ANXIETY (crying); (-) crying may 15 Months


indicate autism spectrum disorder
- walks alone

A. Eruption of the FIRST TEETH: 18 Months

1. Lower Central Incisors: first dental visit - can run and climb stairs

2. Upper Lateral Incisors - closure of anterior fontanelle (DIAMOND)

3. Lateral Incisors NEWBORN

B. Milk Teeth/Deciduous Teeth: TEMPORARY Anthropometric Measurements

- complete at 3 years old a) Head Circumference: 33-35 cm*

- total of 20 teeth b) Chest Circumference: 31-33 cm

- replaced at the age of 6 years old c) Abdominal Circumference: 31-33 cm

NOTE: Jaundice in newborn is normal if it appeared after 24-hours


after birth. It is caused by LIVER IMMATURITY = (-) conversion of
unconjugated bilirubin.
Hyperbilirubinemia Interventions (Phototherapy) 3. To be fed

- remove newborn clothes - to prevent hypoglycemia (Can cause brain damage)

- cover the eyes - NOTE: blood glucose should never be below 40 mg/dL;
ensure uninterrupted breastfeeding.
- cover the genitals
- RA 7600 "Rooming in and Breastfeeding Act of 1992"

RBC Breakdown: Spleen - exclusive breastfeeding: Executive Order 51: Philippine


Milk Code of 1986
Heme: bilirubin (unconjugated): water insoluble
- NOTE: Breastmilk is low in sodium
Globin: ammonia
- colostrum contains IGA (antibodies)
Liver
- introduction of solid foods: 6 MONTHS; intervals: 4-7 DAYS

- NOTE: food should not be mixed in bottle and fed through
Conjugated bilirubin = water soluble a nipple with a large bottle.

Excretion STAGES OF DEVELOPMENT

I. Infant (below 1 year old)

BASIC NEEDS OF NEWBORN Psychosexual: Oral Stage - feeding, pacifier

1. To be warmed Psychosocial: Trust vs. Mistrust - consistent provision of basic needs;


avoid numerous individuals catering the infant's needs.
- to prevent hypothermia and heat loss
Cognitive: Sensorimotor
- NOTE: newborns have poor thermoregulation caused by
less brown fat immature HYPOTHALAMUS Play: Solitary - e.g. rattles, colorful toys

Fear: Stranger

A. Types of Heat Loss

a. Evaporation (evaPOration = punasan) II. Toddler (1-3 years old) - "The Great Imitators"
- when the body is wet, the water evaporates. Psychosexual: Anal Stage - toilet training

- immediate and thorough drying Psychosocial: Autonomy vs. Shame and Doubt

b. Convection (convection = electric fan) - Negativism


- temper tantrum: offer choices, promote safety, ignore
- heat loss due to surrounding air
the behavior
- do not place the newborn in contact with electric fan
Cognitive: Preoperational
c. Conduction (conDuction = dikit)
- egocentrism - inability to see the point of view of others.
- transfer of heat from higher temperature to water temperature
Moral: Preconventional/Premoral
- do not place the newborn in contact with cold surface
Play: Parallel - push and pull toys

Fear: Separation
2. To be protected

- from infection and injury


III. Preschooler (3-6 years old) "Magical Thinkers"
- vaccinations: if temperature reaches 38.5° HOLD
- highest level of curiosity
A. Types of Vaccination
- risk of poisoning: PRIORITY: safety
1. BCG - Tuberculosis
Psychosexual: Phallic Stage - loves the opposite sex, hates the
Site: Right Deltoid same sex.

Psychosocial: Initiative vs. Guild - allows the child to participate.

2. Hepa B - Hepatitis Cognitive: Preoperational - inability to convene.

Site: Vastus Lateralis Moral: Preconventional

Play: Cooperative/Associative - e.g. role playing

3. Vitamin K - Hemorrhage Fear: Body Mutilation

Site: Vastus Lateralis


IV. School Age (6-12 years old)

NOTE: newborns are at risk of bleeding caused by STERILE COLON Psychosexual: Latent - suppressed sex desires

Psychosocial: Industry vs. Inferiority

- support child's activities


- recognize efforts and give compliments
Cognitive: Concrete Operational DEOXYGENTED BLOOD FLOW

- perceptual thinking: making judgments based on what Right Atrium


they see.
- conceptual thinking: making judgments based on ↓
reason.
Right Ventricle
Moral: Conventional

Play: Competitive
Pulmonary Artery → Lungs
Fear: Death, School, Displacement

Ductus Arteriosus
V. Adolescent (12-18 years old) "Puberty Stage"

a. menarche (first menses)
Aorta
b. thelarche (breast development)

c. adrenarche (sexual maturation)


PEDIATRIC NURSING (ABNORMAL)
Psychosexual: Genital
ACYANOTIC HEART DEFECTS
Psychosocial: Identity vs. Role Confusion
- (-) Cyanosis
Cognitive: Formal Operational - hypothetical/abstract - Non – life threatening congenital disorders

Moral: Post-Conventional – morality PATENT DUCTUS ARTERIOSUS

Focus: Body Image - Failure of the Ductus Arteriosus to close at birth

Fear: Peer Rejection - hates parents Manifestations:

- Machinery-like murmur (Note! Can be asymptomatic)


FETAL CIRCULATION
Medical Management:
Fetal Lungs
- Indomethacin
- non-functional (during pregnancy)
- Ibuprofen
- fluid-filled
Surgical Management:
What serves as the fetal lungs during pregnancy?
- Surgical Ligation
- Placenta
COARCTATION OF THE AORTA
Umbilical Cord (AVA)

- has 2 arteries, and 1 vein.


- Narrowing of the Aorta
- Narrowed aorta = Less oxygenated blood in systemic
circulation (compensatory mechanism).

OXYGENATED BLOOD FLOW Manifestations:

Upper Extremities Lower Extremities

Placenta - Bounding pulse - Diminished pulse


- High BP - Low BP

- Cool to touch
Umbilical Vein
- Pallor
↓ - Numbness and tingling

Ductus Venosus

↓ Management:

Inferior Vena Cava


- Balloon Angioplasty

ASTRIAL SEPTAL DEFECT (ASD)
Right Atrium
- Patent foramen ovale, hole in between the Right and
↓ Left atrium

Foramen Ovale Blood from: Superior and Inferior Vena Cava → Right Atrium

↓ Blood from: Left atrium → Right Atrium → Right Ventricle →


Congestion
Left Atrium
Manifestations:

Enlargement of the Right Ventricle → Right Ventricular
Left Ventricle
Hypertrophy

Enlargement of the Pulmonary Artery
Aorta
VENTRICULAR SEPTAL DEFECT (VSD) 4. Overriding of the Aorta - causes mixing of oxygenated and
deoxygenated blood
- Hole in between the Right and Left Ventricle
Manifestations:
Blood from: Right Atrium → Right Ventricle - Cyanosis - NDx: Ineffective tissue Perfusion
- “TET SPELL”
Blood from: Left ventricle → Right Ventricle → Congestion
- Exertional Dyspnea
- Pallor
Manifestations: - Clubbing of fingers
- SCHAMROTH WINDOW TEST
- Enlargement of the Right Ventricle → Right Ventricular
Hypertrophy
- Diminished blood flow to systemic circulation Management:
- Positioning:
• Squatting/Tripoding
Management:
• Knee Chest position
- Application of Dacron Patch - Oxygen therapy: 6-8L/min

PULMONIC STENOSIS HEMATOLOGIC DISORDERS

- Narrowing of the Pulmonic Valve


HEMOPHILIA

Blood from: Right Atrium → Right Ventricle → Pulmonary Artery → - X-linked disorder
Right Ventricular Congestion - FEMALE: Carrier
- MALE: Manifests the disease

Manifestations:
Cause:
- Enlargement of the Right Ventricle → Right Ventricular - Deficiency in clotting factor → Bleeding
Hypertrophy
- Murmur: 2nd ICS, Left
Types:
- Dyspnea
- Diminished blood flow to systemic circulation - HEMOPHILIA A - “Classic Hemophilia”: CF 8
- HEMOPHILIA B - “Christmas Disease”: CF 9
- HEMOPHILIA C - “Rosenthal Syndrome”: CF 11
Management:
- Balloon Angiopathy Manifestations:
- Easy bruising
CYANOTIC HEART DEFECTS - Prolonged bleeding time N:1-10 mins
- Trauma >>> Hemorrhage
- (+) Cyanosis
- HEMARTHROSIS: Bleeding joints - Hallmark sign!
- Life-threatening congenital anomaly
Rest
- Poor supply of oxygenated blood: Systemic Circulation Ice
Compression
Transposition of the Great Arteries or Transposition of the Great Elevate
Vessels (TOGA) - SPONTANEOUS HEMATURIA - Classic Sign

Management:
Right ventricle is connected to: Aorta
- Cryoprecipitate
Left ventricle is connected to: Pulmonary Artery
- Bleeding precautions:
• Avoid contact sports
Manifestations: • Soft bristled toothbrush
- Severe Cyanosis • Use electric razor
- Fatigue
VON WILLEBRAND DISEASE

What makes the patient alive? PDA (Patent Ductus Arteriosus) -


- Bleeding Disorder
allows blood mixing

Cause:
Management:
- Inability of the platelets to adhere → Excessive Bleeding
- Oxygen therapy: 6-8 L/min
- Limit physical activities
- PROSTAGLANDIN E: Alprostadil (keeps PDA open) Problem: Platelet adhesion

Surgical Management: Injury → Bleeding → Platelets will go to the site → Platelet adhesion
- Blalock- Hanlon Operation - surgical procedure to → Forms a Platelet Plug → Stops the bleeding
create PDA
- Jatene Operation / Arterial Switch - complete repair of SICKLE CELL ANEMIA
the vessels
Cause: Irregular-shaped
- RBC - CRESCENT (d/t: presence of HbS-gene )
TETRALOGY OF FALLOT - RBC - Carrier of oxygenated blood
4 PROBLEMS: - Normal: Biconcave
1. Pulmonary Stenosis - primary problem
2. Right Ventricular Hypertrophy - compensatory mechanism Manifestations:
3. Ventricular Septal Defect - keeps the patient alive; decreases - Underweight
pressure in RV - Chronic Anemia
- Fatigue NEURAL TUBE DEFECTS
- Pain

Causes: Failure of the spine to fuse at the center


Management: Deficiency: FOLIC ACID:
- Priority: HYDRATION - Vit. B9
- Avoid: - Valproic acid
• High altitude places
• Cold temperature → Vaso-Occlusive Crisis o
Vigorous exercise ANENCEPHALY
- Oxygen Therapy Absence of skull
Management: Life support
DOWN SYNDROME
SPINA BIFIDA
- “Trisomy 21” Cause:
- Normal Chromosomes: 46 (23 pairs) - Failure of the spine to fuse

Cause: Spina Bifida Occulta


- Extra chromosome at the 21st chromosome - (+) dimpling and tufts of hair
- (-) Paralysis
- (-) Alterations in bowel and bladder function
Manifestations:
- Large protruding tongue → difficulty of feeding →
malnutrition - most common cause of death Spina Bifida Cystica
- Flattened profile - (+) sac
- Simian Crease - (+) paralysis
- Sandal Sign - Alteration in bowel and bladder function
- Short broad neck
- Low set ears
Myelomeningocele - without spinal cord
- Slanted eyes
- Congenital Cardiac Defects Meningocele - spinal cord
- Mental Retardation
Management:
Management: - Prevent damage of the sac:
- Ensure feeding efficacy ➢ Prone
- Watch out for signs of cardiac difficulties ➢ No diapers!
- Parental Support - Apply sterile, moist, non-occlusive dressing

MENINGITIS Complications:
- Inflammation of the meninges - Short term: MENINGITIS
- MENINGES - membrane that covers the brain and spinal cord; - Long term: HYDROCEPHALUS
supports and covers the brain
AMELIA
Causative agents: - Absence of extremities
- Neisseria Meningitidis – common cause! Cause
- Haemophilus Influenzae – bacteria. Prevention: Hib
vaccination - ANTIEMETIC DRUGS: Thalidomide
- Streptococcus Pneumoniae
CLEFT LIP (1st)
- Hereditary
Diagnostics:
Common: MALES
- Lumbar Puncture: Between L4 and L5
- Contraindication: Increased ICP → Brain Herniation Problem:
- Poor sucking ability → malnutrition and aspiration

Manifestations: Management:
- Surgery: Cheiloplasty (2 months) Post-op:
- Irritability
• prevent the infant from crying
- High Pitched Cry
• supine head turned in unaffected side
- Projectile vomiting
- Seizure
- Nuchal Rigidity: Stiff neck CLEFT PALATE (2nd)
- Kernig’s Sign: flexion of knees → hamstring pain - Hereditary
- Brudzinki’s sign: flexion of neck → flexion of the knee
Common: FEMALES
- Opisthotonus: exaggerated arching of the back
- Side-lying position Problem: Speech
Management:
Management - Surgery: Palatoplasty (12-18 months) post-op:
• prone position
- Droplet precaution: Surgical Mask
• avoid use of straw, utensils, popsicles
- Antibiotics
• feed with cups
- Seizure precaution
- Control ICP
• Elevate HOB: Semi-fowler’s HYPERTROPHIC PYLORIC STENOSIS (W/VOMITING)
• Osmotic Diuretic: MANNITOL - Narrowing of the pylorus, thickening of the pyloric
sphincter.
Diagnostic:
- Abdominal Ultrasound
CELIAC DISEASE
Manifestations: - Gluten sensitive enteropathy; gluten intolerance;
- upper abdominal distention irreversible
- projectile vomiting - severe abdominal distention
- non-bilous vomitus
- signs of dehydration Diagnostic:
- metabolic alkalosis - Bowel Biopsy
- malnutrition and weight loss Manifestations:
- visible peristaltic movement (left to right) - diarrhea
- olive-shaped mass (RVQ) - steatorrhea (increase fat content in feces

Management: NO GAS FORMING FOOD! Management


- increase oral fluid intake
- Avoid food with gluten: BROW (Barley, Rye, Oats, Wheat)
- assess the vomitus
- No processed food
- positioning: high fowler’s
CYSTIC FIBROSIS
Surgical Management:
- Inherited genetic disorder
- Pylorotomy (Ramstedt Operation)
PROBLEM: all secretions are viscous
INTUSSUSCEPTION (W/PAIN)
Organs Affected:
- Telescoping of the colon
- Intestines
SITE: - Lungs
- Skin
- Ileocecal Valve (boundary between the small and large - Pancreas
intestine)
Manifestations:
Diagnostic:
- meconium ileus
- Barium Enema - thick bronchial secretions
- Guaiac’s Test - DOB
- very salty sweat (increased na)
Manifestations: - acute pancreatitis
- sudden abdominal pain (colicky)
- abdominal distention Management:
- red-currant jelly stool - Chest physiotherapy (requires MD order)
- sausage-shaped mass (RVQ) - Pancreatic enzymes – after meals

Management: Complications:
- Females: Decreased Fertility
- assess bowel sounds (borborygmus)
- Males – Sterility
- assess abdominal distention
- NGT insertion (for decompression)
WILM’S TUMOR
CANCER: Kidney “Nephroblastoma”
Surgical Management:
- Laparotomy “Surgical Resection of Colon”
Manifestations:
- abdominal mass
- fatigue
HIRSHSPRUNG’S DISEASE
- high BP
- A ganglionic megacolon - hematuria

CAUSE: Management:
- constant monitoring of BP 4-6qhr
- Absence of ganglion → peristalsis movement, nutrients - NEVER palpate the abdomen
absorption
URINARY TRACT INFECTION
Diagnostic:
CAUSE: Escherichia coli (E-coli)
- Rectal Biopsy COMMON: Females: Shorter length of urethra (2-3 inches); males:
6-9 inches
Manifestations:
Manifestation:
- (-) peristalsis - dysuria/burning sensation
- enlarged colon: SIGMOID - cloudy urine
- fecal-shaped mass (LLQ) - hyperthermia
- bile-stained foul-smelling emesis
- foul breath Complications:
- malnutrition - cystitis
- pyelonephritis
Management:
Management:
- high caloric diet
- Antibiotic
- assess the stoma (normal: pinkish) (necrosis: bluish/gray –
report)
Prevention:
- colostomy care:
- increase fluid intake
• size: 1/8 larger than the stoma
- avoid holding urine
• emptying: 1/3 - ½ full
- avoid acidic drinks
Surgical Management: - good perineal hygiene

- Swenson Pull-Through
- AVOID allergens
GABH’s (Group A Beta Hemolytic Streptococcus) Infections
FEBRILE SEIZURES
TONSILLITIS
- inflammation of the tonsillitis. CAUSE: high fever: > 38.5
- too much glucose which attracts microbes
- throat swabs OTHER CAUSE: immaturity of hypothalamus
- dysphagia,
- hyperthermia Management:
- seizures precautions
ADENIODITIS - during seizure episode:
- inflammation of the adenoids • PROMOTE SAFETY:
- cold weather ➢ remove pillows o never restraint the child
- nasal swab ➢ maintain patent airway: side-lying position
- dysphagia, - anticonvulsant medications:
- hyperthermia • Phenytoin (Dilantin) o therapeutic level: 10-20
mg/dL newborn: 8-15 mg/dL o never stop abruptly,
Complications: taper
- bacteremia ➢ status epilepticus
- endocarditis
- GN (acute glomerulonephritis) Complications
- Gingival Hyperplasia
Management: • Use soft bristled toothbrush
- antibiotics • Oral care
- increased fluid intake
- gargling solutions

Surgical Management:
- Tosillectomy
- Adenoidectomy post-op:
• side-lying position
• WOF: signs of bleeding
➢ frequent swallowing
➢ drooling of blood
➢ hypotension
➢ tachycardia
➢ tachypnea
• avoid food that may induce coughing
• avoid blowing of nose

EPISTAXIS (Nose Bleeding)


- Trauma in the anterior part of the nose

Management:
- lean forward
- apply pressure on the soft tissue part of the nose (at least 5
mins)
- apply cold compress

BRONCHIAL ASTHMA
- Reversible

CAUSE: Allergens

Pathophysiology

Allergen → Activation of Immune Response



Inflammation: Bronchus
Leukotriene ← → Histamine
↓ ↓
Bronchoconstriction Swelling: Goblet Cells
↓ ↓
Wheezing (expiration) Increased mucus production

Airway obstruction

Reduced O2 supply in the body

Manifestations:
- hyperventilation → respiratory alkalosis (initially) →
respiratory acidosis
- DOB
- dyspnea
- use of accessory muscles

Management
- orthopneic position
- bronchodilators: albuterol (short term m/x)
- oxygen therapy (short term m/x)
- corticosteroids “sone” (beclomethasone)

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