Professional Documents
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Families are smaller in Fewer family members 1. Birth rate - no. of births per 1000 population
size are present as support
2. Fertility rate - no. of pregnancies per 1000
people in times of crisis
women of childbearing age
Role of Nurse: Fulfill the 3. Fetal Death Rate- no. of fetal deaths weighing
role more than 500g or more per 1000 live births.
4. Neonatal Death Rate- neonatal period (1st 28
Increased Single Parents Fewer financial resources days of life). No. of deaths per 1000 live births
(most common type of esp. woman
occurring in the 1st 28 days of life.
parent in US)
Role of Nurse: Inform a. to declare a neonatal death rate, it
parents of care options must be based on the age of gestation
and back-up opinion. and weight (dead )
5. Perinatal Death Rate - Perinatal period (6 weeks
Increased mothers Healthcare must be before conception and 6 weeks after childbirth).
MATERNAL AND CHILD NURSING II
WEEK 1 ONLINE LECTURE | Prof. Maria Lourdes B. Balleza.RN.MAN
No. of deaths of fetuses weighing > 500g and c. lack of emergency transportation
within the 1st 28 days of life per 1000 birth. (ambulance use for life and death
6. Infant Mortality Rate - no. of deaths per 1000 situation which is not for labor in
live births in the first 12 months of life pregnancy, lack of physical ambulance )
7. Childhood Mortality Rate - no. of deaths per d. lack of awareness of existing services
1000 population in children 1-14 y/o (hindi nalalaman ng pasyente na pwede
8. Maternal Mortality Rate - no. maternal deaths pala siya sa barangay health center, not
per 100,000 live births that occur as a direct informed)
result of the reproductive process. e. lack of community support (lack of
trainees and volunteers, kakaunti na
Risk of Maternal Death are Affected by many Factors lang yung nae-engage o naiingganyo)
● Frequency and spacing of births 3. DELAY IN MANAGEMENT OF COMPLICATIONS
● Nutrition level (maternal undernutrition) a. lack of health care providers (may mga
● Sta ture and maternal age namatay na doktor, dahil sa fear of
● Appropriate medical and midwife support covid before marami ang hindi
● Access to emergency and intensive treatment if nagtrabaho as healthcare provider)
were necessary b. shortage of supplies (dahil sa demand)
● Lack of management capacity in the health c. lack of equipment (hindi nakakabili ang
system ospital, kaya dun pupunta yung
● No political will and lack of management pasyente sa isang hospital na kumpleto
capacity in the health system at kayang gampanan ang kanilang
pangangailangan)
> Majority of the deaths and disabilities are preventable, d. lack of competence of health providers
being mainly due to insufficient care during pregnancy (dahil sa nagsarang training centers
and delivery. kaya most of the practices ay natutunan
> HIV infection is an increasing threat. Mother-to-child online and reading books, which are
transmission of HIV continues to be a major problem, not effective enough)
with up to 45 percent of HIV infected mother’s e. weak referral system
transmitting infections to their children
DOH’s Essential Package of Child Survival Interventions
Three Delays that Lead to Maternal and Neonatal ● Skilled attendance during pregnancy, childbirth
Deaths and the immediate postpartum
1. DELAY IN IDENTIFICATION OF COMPLICATIONS ● care of the newborn
a. failure to recognize danger signs ● breastfeeding and complementary feeding
b. lack of money ● micronutrient supplementation
c. unplanned/ unwanted pregnancy ● immunization of children and mothers
d. lack of companion in going to health ● integrated management of sick children
facility ● birth spacing
e. no person to take care of children/
home DOH Program/ Interventions for Child Care
f. fear of being ill treated in health facility ● Early essential newborn care
2. DELAY IN REFERRAL ● Infant and young child feeding
a. distance from a woman’s home to ● newborn screening (na ginawang law, required
health facility/ provider (malayo) to be done sa isang newborn)
b. lack of/ poor condition of roads (nasa ● integrated management of childhood illness
barrio nakatira, lubak-lubak na daan) ● immunization program
MATERNAL AND CHILD NURSING II
WEEK 1 ONLINE LECTURE | Prof. Maria Lourdes B. Balleza.RN.MAN
7. Balance between modern technology and ● In humans, each cell, except for the sperm and
quality ovum, contains 46 chromosomes (22 pairs of
autosomes and 1 pair of sex chromosomes)
NOTE: we as nurses, we should be sure that everything is ● Spermatozoa and ova each carry only half of
documented and we cannot judge or dictate the mother the chromosomes number or 23 chromosome.
on what will be her decision. Kung anong gusto niyang For each chromosome cell, there is a like
gawin sa anak niya bahala siya, and how will you protect chromosome of similar size and shape and
yourself as a nurse, may mga consent forms to prevent function (autosome or homologous
you from being involved by law. Ex: The doctor wants a chromosome) in the ovum
tissue from the placenta of the mother, as nurse we are ● Because genes are always located at fixed
the patient’s advocate, bago magawa ng doctor ang positions on chromosomes, two like gene
pagkuha ng tissues or any part of the body we should (alleles) for every trait that are represented in
always ask their permission with a consent form, with the ovum and sperm on autosomes. The one
that we could prevent ourselves as nurses from being chromosome in which this does not occur is the
involved sa lawsuit na tinatawag na (BATTERY) chromosome for determining gender
● if the sex chromosomes are both type X (large
GENETICS AND GENETIC COUNSELING symmetric) in the zygote formed from the union
Genetics disorders of a sperm and ovum = FEMALE
● are disorders that can be passed from one ● if one sex chromosome is an X and one is a U
generation to the next (smaller type), = MALE
● result from some disorder in gene or ○ ang tatay ang nagdedetermine ng
chromosome structure and occur in 5% to 6% of gender ng bata
newborn ● A person’s phenotype refers to his or her
outward appearance or the expression of genes
Genetics ● A person’s genotype refers to his or her actual
● study of heredity, and the variation of inherited gene composition
characteristics ○ impossible to predict a person’s
genotype from the phenotype
Cytogenetics ● A person’s genome is the complete set of genes
● study of chromosomes by light microscopy and present or a normal genome is abbreviated as
the method by which chromosomal aberrations 46XX or 46XY
are identified ●
LEA:
A. Nature of Inheritance 4. X-Linked Recessive Inheritance
Genes ● Most X-linked inherited disorders are NOT
● basic units of heredity that determines both the Dominant, but Recessive.
physical and cognitive characteristics of people ● When the inheritance of a recessive gene comes
● it is composed of segments of DNA, they are from both parents (homozygous recessive), it
woven into strands in the nucleus appears to be incompatible with life. Therefore,
females who inherit the affected gene will be
Chromosomes heterozygous, and, because a normal gene is
● are threadlike structures of nucleic acids and also present, the expression of the disease will
protein found in the nucleus of most living cells, be blocked. On the other hand, because males
carrying genetic information in the form of have only one x chromosome, the disease will
genes be manifested in any male children who receive
the affected gene from their mother.
MATERNAL AND CHILD NURSING II
WEEK 1 ONLINE LECTURE | Prof. Maria Lourdes B. Balleza.RN.MAN
● So, sa x-linked recessive, ang nagkakaroon ng ● Meiosis is the type of cell division in which the
manifestation ay yung mga male children. number of chromosomes in the cell is reduced
a. 50% that a male child will manifest the disease to the haploid (Half) number for reproduction
b. 50% that a female child will carry the disease (i.e 23 rather than 46 chromosomes)
gene ● All sperm and ova undergo a meiosis cell
● If the father has the disease, and chooses a division early in formation. The cell then divides
sexual partner who is free of the disease gene, cleanly, with 23 chromosomes in the first new
the chances are 100% that a daughter will have cell and 23 chromosomes in the second new
the sex linked recessive gene, but there is no cell.
chance that a son will have the disease. ● Chromosomal abnormalities occur if the division
is uneven (nondisjunction). The results may be
5. Multifactorial (Polygenic ) Inheritance that one new sperm cell or ovum has 24
● Many childhood disorders such as heart disease, chromosomes and the other has only 22.
diabetes, pyloric stenosis, cleft lip, and palate, ● If a spermatozoon or ovum with 24 or 22
neural tube disorders, hypertension and mental chromosomes fuses with a normal
illness tend to have a higher than usual spermatozoon or ovum, the zygote (sperm and
incidence in some families. They appear to occur ovum combined) will have either 47 or 45
from multiple gene combinations possibly chromosomes, not the normal 46.
combined with environmental factors.
● Pag sinabi natin na idiopathic (means na Chromosomal Abnormalities because of Nondisjunction.
unknown yung cause) yung reason bakit meron a. Down Syndrome / Trisomy 21 Syndrome
siyang diabetes, it because of the multifactorial (47XY21 + or 47XX21+)
inheritance. Hindi siya masyadong kinoconsider ● Trisomy 21, the most frequently occurring
as part of Mendelian Inheritance because this chromosomal disorder, occurs in about 1 in 800
one is affected not primarily because of the pregnancies. In women who are older than 35
chromosomes and genes, but because of years of age, the incidence is as 1 in 100 live
environmental factors like stress, diet, pollution. births. The physical features of children with
Natritriger lang siya lumabas (yung condition) down syndrome.
dahil sa mga environmental factors. ● Kadalas na tinitingnan or chinecheck para
● Diseases caused by multiple factors this way do malaman if mongoloid ay ang “Single Palm
not follow Mendelian Laws because more than a Crease”. Also facial features: Abnormal ears, Flat
single gene or Human Lymphocyte Antigen (HLA) back of head.
is involved. Their incidence is so unpredictable.
Chromosomal Abnormalities
(Cytogenic Disorders)
In some instances of genetic disease, the
abnormality occurs not because of dominant or recessive
gene patterns but through a fault in the number or
structure of chromosomes, which results in missing or
distorted genes. When chromosomes are photographed
and displayed, the resulting arrangement is termed as
KARYOTYPE.
NONDISJUNCTION ABNORMALITIES
MATERNAL AND CHILD NURSING II
WEEK 1 ONLINE LECTURE | Prof. Maria Lourdes B. Balleza.RN.MAN
Deletion Abnormalities
Deletion abnormalities are a form of chromosome
disorder in which part of a chromosome breaks during
cell division, causing the affected person to have the
MATERNAL AND CHILD NURSING II
WEEK 1 ONLINE LECTURE | Prof. Maria Lourdes B. Balleza.RN.MAN
number of chromosomes plus or minus an extra portion 1. provide concrete accurate information about the
of a chromosome, such as 45.75 chromosomes or 47.5. process of inheritance and inherited disorders.
2. reassure people who are concerned that their
a. Cri-du-chat syndrome (46xy5p-) children may inherira particular disorder.
3. allow people who are affected by inherited
● in cri-du-chat syndrome (46xy5q), one portion of disorders to make informed choices about
chromosome 5 is missing. future reproduction.
○ abnormal cry (sound of a cat than 4. allow people to pursure potential intervention
human) that may exist such fetal surgery
○ small head 5. allow families to begin preparation for a child
○ wide-set eyes with special needs
○ downward slant palpebral fissure of the
eye
○ recessed mandible
○ severely cognitively challenge