10 July 2009

Respiratory System



Respiratory System

Respiration
* Process of air exchange
* Oxygen is obtained and carbon dioxide is eliminated
* Gas exchange occurs in the alveoli

Four parts of respiration
* Ventilation – movement of air between the atmosphere and alveoli
* Perfusion – blood flow through the lungs
* Diffusion – oxygen and carbon dioxide are transferred between alveoli and blood
* Regulation – respiratory muscles and nervous system

Respiratory Tract
* Nose, pharynx, larynx, trachea, bronchi
* Series of tubes that function as airway passages
* Filter, warm and humidify incoming air

Epiglottis
Heimlich Maneuver
Heimlich Maneuver - Infant
Trachea
Cilia - Smokers
Lungs
Bronchi
Alveoli
Surfactant
Lack of Surfactant
Nervous System Role
Disorders of Respiratory System
Drugs for Asthma and Broncho-constrictive Disorders
Asthma
* Airway disorder characterized by
o Hyper-reactivity to various stimuli - trigger
o Broncho-constriction
o Inflammation
Clinical Manifestations - Asthma
Precipitating Factors - Triggers
Pathophysiology
Drug to Treat Asthma
Quick Relief

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Skin – Immune Disorders



Skin – Immune Disorders
By:Jan Bazner-Chandler
CPNP, CNS, MSN, RN

Key Function of Skin
* Protection – shield from internal injury.
* Immunity – contains cells that ingest bacteria and other substances.
* Thermoregulation – heat regulation through sweating, shivering, and subcutaneous insulation
* Communication / sensation / regeneration

Developmental Variances
* Sweat glands function by the time the child is 3-years-old.
* The visco-elastic property of the dermis becomes completely functional at about 2 years.
* The neonate’s dermis is thin and very hydrated, thus is at greater risk for fluid loss and serves as an ineffective barrier.

Diagnostic Tests
* Cultures
* Scraping
* Skin biopsy
* Skin testing
* Woods lamp
Neonatal skin lesions
* Vascular birth marks: hemangioma
* Port wine stain
* Abnormal pigmentation: Mongolian spots
* Neonatal acne: small red papules and pustules appear on face trunk.
* Milia: white or yellow, 1-2mm papules appearing on cheeks, nose, chin, and forehead
Inflammatory Skin Disorders
* Diaper dermatitis
* Contact dermatitis
* Atopic dermatitis or eczema
Cradle Cap
Treatment
Baby Care
Acne Vulgaris
Management of Acne
Pediculosis
Signs and Symptoms
Nits
Empty nit case
Viable nit
Interventions
Scabies
Assessment
Management
Impetigo
Causative agent
Spread
Interventions
Outcomes
Impetigo / cellulitis
Clinical Manifestations
Poison Oak, Ivy and Sumac
Poison Ivy
Poison Oak

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Drugs Affecting Respiratory System



Drugs Affecting Respiratory System
By:Jan Bazner-Chandler MSN, CNS, RN, CPNP

Common Cold
* Most cold are caused by viral infections
o Rhinovirus
o Influenza
* Virus invade the mucosa of the upper respiratory tract, nose, pharynx and larynx which leads to the upper respiratory system.
* Signs and symptoms: excessive mucous production leads to sore throat, coughing, upset stomach.
* Treatment: reduce symptoms
* Note: antibiotics do not help viral infections

Echinacea
* Herbal Therapy
* Has been shown in clinical trials to reduce cold symptoms and recovery time when taken early in the illness.
* Adverse effects: dermatitis, upset stomach, dizziness, headache, and unpleasant taste.

Antihistamines
* Action: act directly on histamine receptor sites H1 blockers.
* Used as an inflammatory mediator for allergic disorders, allergic rhinitis (hay fever and mold, and dust allergies), anaphylaxis, angioedema, insect bites and urticaria (itching).

Antihistamines
* Antihistamines associated with sedation (CNS)
* Non-sedating antihistamines

Antihistamines: sedating
* Classification: H1 antihistamine
o chlorphenramine (Chlor-Trimeton)
o dephenhydramine (Benadryl)
diphenhydramine

* Trade name: Benadryl
* One of the oldest anti-histamines
* Action: Antagonizes the effects of histamine at the H1 receptor sites.
* Adverse Effects: Significant CNS depressant: drowsiness, dizziness, hypotension, dry mouth.
o Onset: immediate to 60 minutes
o Peak: 1-4 hours
o Duration: 4-8 hours

Non-sedating Antihistamine
* The drugs were developed to eliminate the unwanted adverse effects; mainly sedation.
* Action: Works peripherally (do not cross the blood brain barrier) to block the actions of histamine.

loratadine
* Generic name: loratadine
* Trade name: Claritin
* Action: blocks peripheral effects of histamine released during allergic reactions.
* Therapeutic Effects: decreased symptoms of allergic reactions (nasal stuffiness, red swollen eyes)
o Onset within 1-3 hours
o Peak within 8-12 hours
o Duration: > 24 hours

cetirizine
* Trade name: Zyrtec
* Therapeutic classification: allergy, cold, and cough remedies, antihistamine
* Action: Antagonizes the effects of histamine at H1-receptor sites; anticholinergic effects are minimal.
o Onset: 30 minutes
o Peak: 4-8 hours
o Duration: 24 hours

Decongestants
* Nasal congestion is due to excessive nasal secretions and inflamed and swollen nasal mucosa.
o Three types of decongestants
+ adrenergic
+ anticholinergic
+ corticosteroids

Route of administration

* Orally to produce systemic effect
* Inhaled: directly to lungs with some systemic effects
* Nasally: local with some systemic effects

Nasal Drugs

* Adrenergic Drugs: topical application directly into the nares provides a very potent decongestive effect.
* Main side effect: rebound effect (after a few days of use if discontinued can have rebound congestion).

Adrenergic Nasal Drugs
* Afrin
* Neo-Synephrine
* Sinex

Intranasal Steroids
* Often used prophylactically to prevent nasal congestion in patients with chronic upper respiratory tract infections.
* Action: aimed at the anti-inflammatory response
* Trade names
o Nasacort
o Flonase
o Nasalide

Drugs to Treat Coughs
* Antitussives
o Opioid
o Non-opioid
* Expectorants

Antitussive Drugs
* Opioid drugs all have antitussive effects
* Codeine is the only opioid used as a cough medicine
* Action: suppress the cough reflex through direct action on the cough center in the CNS (medulla).
* Adverse effects: CNS and respiratory depression and addictive potential

Antitussive Drugs
* Non opioid
* Generic: dextromethorphan
* Trade names:
o Vicks Formula 44
o Robitussin DM
o Safe, non-addicting and does not cause CNS or respiratory depression.

Expectorants
* Aid in the coughing up and spitting out of the excess mucous that has accumulated in the respiratory tract by breaking down and thinning the secretions.
* Action:
o Loosening and thinning the respiratory tract secretions
o Direct stimulation of the secretory glands in the respiratory tract.
* Guaifenesin is the only drug currently available.
* Trade names: Robitussin, Humibid, Guiatuss
* Therapeutic effect: relief of respiratory congestion and cough suppression

Bronchodilators and Other Respiratory Drugs

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Pediatric Malignancies



Pediatric Malignancies
By:Jan Bazner-Chandler
CPNP,MSN, CNS, RN

Pediatric Malignancies
Causes
* Genetic alteration
* Environmental influences
* No know prevention
* Metastasic disease
Response to Treatment
Classification of Tumors
Cardinal Signs of Cancer
* Unusual mass or swelling
* Unexplained paleness and loss of energy
* Spontaneous bruising
* Prolonged, unexplained fever
* Headaches in morning
* Sudden eye or vision changes
* Excessive – rapid weight loss.
Diagnostic Tests
* X-ray
* Skeletal survey
* CT scan
* Ultrasound
* MRI
* Bone marrow aspiration
Biopsy
* Identify cell to determine type of treatment
Treatment Modalities
* Determined by:
o Type of cancer
o Location
o Extent of disease

Surgery
Radiation Therapy
Chemotherapy
Administration
Goals of Chemotherapy
Chemotherapy Drugs
Bone Marrow Transplant
Gene Therapy

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Gastrointestinal Disorders



Gastrointestinal Disorders
By:Jan Bazner-Chandler
CPNP, CNS, MSN, RN

Embryonic Development
* Failure to fuse = cleft lip and palate
* Failure to differentiate = duodenal stenosis
* Atresia or abnormal closing of structure:
o Esophogeal atresia
o Anal-rectal malformation
o Biliary atresia

Fetal Development
* Fistula is an abnormal connection
* Incomplete or abnormal placement
Prenatal History
* Birth weight
* Prematurity
* History of maternal infection
* Polyhydramnios
* Down Syndrome
Health History
* Congenital anomalies
* Growth or feeding problems
* Travel
* Economic status
* Food preparation
* General hygiene
* Family history of allergies

Present Illness
* Onset and duration of symptoms
* Weight loss or gain
* Recent changes in diet
Vomiting
Nursing Assessment
* Abdominal distention
* Abdominal pain
* Abdominal assessment
Measuring Abdominal Girth
Bowden Text
Diagnostic Tests
* Flat plate of abdomen
* Barium swallow or UGI
Diagnostic Tests
* Ultrasound
* CT scan = tumors, abscess, obstruction
* 24 hour probe = Gastro esophogeal reflux
* Biopsy of liver, esophagus, stomach, intestine
Stool and Blood
* White blood cells
* Ova and Parasite
* Bacterial cultures
* Blood

FTT
Cleft Lip and Palate
Incomplete fusion of the primitive oral cavity
Feeding
Post Surgery Care
Cleft Lip Repair
Cleft Palate
Palate Repair
ESSR
Devices For Feeding
Whaley & Wong
Post Surgery Repair
Long Term Referrals
Esophageal Atresia
Failure of the esophagus
Clinical Manifestations
X-ray Findings
Pre-surgery Care
Post Surgery Care
Ball & Bindler
Post Operative Care
Long Term Complications
Pyloric Stenosis
Clinical Manifestations
Management Pre-surgery
Feeding Post-operatively
Hernias
Inguinal Hernia
Hydrocele
Umbilical Hernia
Diaphragmatic Hernia
Clinical Manifestations
X-ray Diaphragmatic Hernia

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Before and after fistula repair



Before and after fistula repair

Tracheoesohpageal fistula

An omphalocele is an abdominal wall defect at the base of the umbilical cord (umbilicus); the infant is born with sac protruding through the defect which contains small intestine, liver, and large intestine.

Gastroschisis:
Surgical repair of abdominal wall defects involves replacing the abdominal organs back into the abdomen through the abdominal wall defect, repairing the defect if possible, or creating a sterile pouch to protect the intestines while they are gradually pushed back into the abdomen.

Anorectal malformations; Anal atresia
Imperforate anus is a relatively common congenital malformation that occurs in about 1 out of 5,000 infants.
signs & symptoms
o absence of anal opening
o misplaced anal opening
o anal opening very near the vaginal opening in the female
o no passage of first stool within 24 to 48 hours after birth
o stool passed by way of vagina or urethra
o Abdomianl distention
o vomiting if infant is fed
o Asymmetry in leg positions
o Asymmetry of the thigh fat folds
o After 3 months of age, asymmetry of rotation of the leg and apparent shortening of the affected leg
o Diminished movement in the affected side

Signs & tests
Pediatricians routinely screen all newborns and infants for hip dysplasia. There are several maneuvers that can detect a dislocated hip or a hip that is able to be dislocated. A hip that is truly dislocated in an infant should be picked up but some cases are subtle and some develop after birth, which is why multiple examinations are recommended. Some mild cases are "silent"; and cannot be picked up on physical exam.

Ultrasound of the hip is the most important imaging study and will demonstrate hip deformity. A hip X-ray joint X-ray) is helpful in older infants and children.

Treatment
In early infancy, positioning with a device to keep the legs apart and turned outward (frog-leg position) will usually hold the femoral head in the socket. If there is difficulty in maintaining proper position, a plaster cast may be applied and changed periodically to accommodate growth. Operative management may be necessary if early measures to reduce the joint (put the joint back in place) are unsuccessful, or if the defect is first detected in an older child.

Prognosis
If the dysplasia is picked up in the first few months of life, it can almost always be treated successfully with bracing. In a few cases surgery is necessary to put the hip back in joint.The older the age at diagnosis, the worse the outcome and the bigger the surgery needed to repair the problem.

Talipes equinovarus; Talipes or Clubfoot

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Neonatal Surgery



Neonatal Surgery
By:Juan E Gonzalez, CRNA, MS, ARNP
Based on prior lecture by
John P. McDonough, CRNA, Ed.D., ARNP
Professor & Director
Anesthesiology Nursing

Anatomical Differences
Pedi vs. Adult Airway
More Vertical
Less vertical
R mainstem bronchus
V-shaped
U-shaped
Shape of Epiglottis
Glottis
Cricoid
Narrowest Point
C3-C6
C2-C4
Laryngeal location

Head Position
Visual Alignment of Oral/Pharyngeal/Laryngeal axes
Attempt to achieve “sniffing” position will OBSTRUCT pt
Intubation
To intubate or not to intubate…
Is that a question??
Choice of Intubating Technique
Choice of Intubating Technique
(patient factors)
Blood Pressure Control

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Abdominal Wall Defects: Omphalocele vs. Gastroschisis



Abdominal Wall Defects: Omphalocele vs. Gastroschisis
By:Joanna Thomson,
Surgery Clerkship

Embryology Review
* The Midgut gives rise to:
o Duodenum distal to the bile duct
o Jejunum
o Ileum
o Cecum
o Appendix
o Ascending colon
o Hepatic flexure of the colon
o Proximal two-thirds of transverse colon.

Physiological Umbilical Herniation
* As a result of rapid growth and expansion of the liver, the abdominal cavity temporarily becomes too small to contain all the intestinal loops.
* The intestinal loops enter the extraembyronic cavity within the umbilical cord during the sixth week of development.
* As herniation occurs, the loop undergoes a 90 degree counterclockwise rotation around the superior mesenteric artery.

Return to Abdominal Cavity
* During 10th week of development, herniated intestinal loops begin to return to the abdominal cavity.
* Undergoes additional 180 degree counterclockwise rotation about the superior mesenteric artery.
* Factors responsible for this return are not precisely known... It is thought that regression of the mesonephros (kidney), reduced growth of the liver, and expansion of the abdominal cavity all play roles.

Omphalocele
* Herniation of abdominal viscera through an enlarged umbilical ring.
o Failure of the bowel to return to the body cavity following physiological umbilical herniation. Defective mesodermal growth causes incomplete central fusion and persistent herniation of the midgut.
* Extruded viscera may include LIVER, small and large intestines, stomach, spleen, or bladder.
* Covered by amnion and peritoneum

Gastroschisis
* Herniation of intestinal loops through the anterior abdominal wall.
* Defect lateral to the umbilicus (right>left)
o Abnormal involution of the right umbilical vein or vascular accident involving the omphalomesenteric artery causes localized abdominal wall weakness.
* No sac covers the extruded viscera.

Prenatal Diagnosis
* Elevated maternal serum alpha fetoprotein
* Ultrasound
Omphalocele Gastroschisis

Epidemiology

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05 July 2009

Sexually Transmitted Diseases What’s New?



Sexually Transmitted Diseases What’s New?
By:Linda Creegan, FNP
California STD/HIV Prevention Training Center


Common STDs

* Humanpapilloma Virus
* Trichomoniasis
* Chlamydia
* Genital herpes
* Gonorrhea
* Hepatitis B
* Syphilis

Overview of Complications of Sexually Transmitted Diseases

Fetal Wastage*
Low Birthweight*
Congenital Infection*
Upper Tract Infection
Systemic Infection
STDs
Infertility
Ectopic Pregnancy*
Chronic Pelvic Pain
HIV Infection*
Cervical Cancer*
* Potentially Fatal
Increased Transmission of HIV in the Presence of Other STDs
* Transmission increased 3-5 times
* Increased susceptibility
* Increased infectiousness
Chlamydia
Gonorrhea
Risk Factors
Recommendations
Syphilis
P&S Syphilis
Genital Herpes
Herpes simplex virus type 2
Genital Warts
What’s New with Chlamydia Infection?
Chlamydia Infections in Women and Neonates
Genital Chlamydia in Women: Complications
Untreated genital CT infection
Ectopic pregnancy
Infertility
Chronic pelvic pain
Public Health Approaches to Chlamydia Control
Chlamydia Screening & Treatment
CT Screening Cost-Effective
Chlamydia Screening Recommendations
Chlamydia Testing Current Diagnostic Methods
Chlamydia Testing Nucleic Acid Amplification Tests
Hybrid Capture
Genital Chlamydia Diagnostic Tests
Sensitivity
Urine-Based CT Tests
Cost Effectiveness of NAAT
Chlamydia Follow-up
Is Test-of-Cure Necessary?
Chlamydia Partner Management
What’s New with Gonorrhea?
Gonorrhea Infection
Gonorrhea Clinical Presentation
Gonorrhea Complications

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Forensic Serology



Forensic Serology

Forensic serology is the application of the study of blood, semen, saliva and other body fluids, to legal matters. The field generally is comprised of the detection of enzymes and antigens, as in the identification of seminal stains or blood typing (ABO and secretor status) and DNA typing (by PCR or RFLP analysis).

The serology section of a forensic laboratory may deal with any or all of the following:
* blood typing
* characterization of unknown blood
* blood spatter analysis for crime reconstruction
* paternity testing
* semen identification in rape cases
* DNA techniques used for identification

The Composition of Blood
Blood is a mixture of many components:
cells inorganic substances (salts)
enzymes water
proteins
Forensic Characterization of Bloodstains
Three questions that must be answered by the forensic investigator:
1) Is it blood? Use presumptive tests:
Kastle-Meyer
Leuchomalachite Green
Luminol
2) Is it human blood?
Precipitin Test
3) Can it be associated with an individual?
DNA

Is It Blood? Presumptive Tests for Blood

Luminol
* Red blood cells contain hemoglobin (Hb) – the protein responsible for transporting oxygen
* Each Hb contains four iron (Fe) containing hemes
False Positives
Precipitin Test Procedure

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Male Reproductive Problems



Male Reproductive Problems
By:Fertilization Specialists
Joshua Prince
Preston Moore
Candace Lindler

Infertility
* Infertility is the inability of a couple to become pregnant

Treatment
Normospermia with functional defects
Asthenospermia and teratozoospermia
Oligospermia
Untreatable subfertility
Reversible toxin effects
Disorders of sexual function
Gonadotropin deficiency
Obstructive azoospermia
Sperm autoimmunity
Treatable conditions
Primary seminiferous tubule failure
Untreatable sterility
FREQUENCY (%)

TYPE OF INFERTILITY
Table 1. Classification Of Male Infertility By Effectiveness Of Medical Intervention To Improve Natural Conception Rate
* Sperm count equals the number of sperm per cm3 or cc
* The average has dropped in the past 20 years
* 85-90% are treated with medication or surgery
* Lifestyle changes

Normal Reproduction
* Ovulation
* Spermatogenesis
* Sperm meets with egg in fallopian tube
* Fertilization
* Implantation

Male Reproductive System
Female Reproduction System
Normal Spermatogenesis
Testes
* Spermatogonium (2N)
Differentiation
* Primary Spermatocyte (2N)
Meiosis I
* Secondary Spermatocytes
Meiosis II
* Spermatids
Differentiation
* Spermatozoa
Spermatogenesis
* Seminferous Tubules
90% of the testis
* Thousands of sperm per second although spermatogenesis 8-10 weeks
* Stored for months
* Degraded and deposited into the circulatory system if not ejaculated
Klinefelter Syndrome
* XXY instead of XX or XY
* usually male
* lower levels of testosterone
* improper formation of semineferous tubules

Bilateral Anorchia
* vanishing testes syndrome
* testes originally present but reabsorbed before or after birth
Oligospermia
* having too few sperm
* due to:
fever
excessive alcohol
smoking
varicocele
orchitis

Azoospermia
* total lack of sperm in ejaculate
* due to:
fever
undescended testicle
obstructions of seminal vesicles
testicle infection

Cryptorchidism
* 30% of males born premature
* 3% of males carried to term
* Predisposes the person to risk of torsion
* Androgen receptor
* Bilateral has six times the impact on infertility
* Increase in Temperature
* Testicular atrophy
* Treated at Childhood

Abnormalities
* Testicular torsion
of the spermatic cord cuts off the venous drainage, leading to hemorrhagic infarction
It is the twisting of the spermatic cords
Immediate treatment
* Testicular cancer

Illnesses
* Acute
* Chronic
Orchitis
STDs
* Fibropapilloma
Stimulants
Age
Gynecomastia
* Testicular Failure
* Androgen receptors
* Cirrhosis
* Tumors
* Illegal steroid
* Feminine characteristics

Examination

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Using NCCLS Standards to Create Procedure Manuals



Using NCCLS Standards to Create Procedure Manuals
by:Mary E. Gray

What is NCCLS?
* A nonprofit, educational organization that provides a communication forum for the development, promotion and use of national and international standards.
* Founded in 1968 and accredited by the American National Standards Institute.
Why NCCLS?
* Based on the principle that voluntary consensus standards are essential for performing clinical laboratory testing at the high level necessary for quality patient care
* Describes laboratory procedures, bench and reference methods, and evaluation protocols applicable within all the major laboratory disciplines

What are the different types of publications?
* Standard: clearly identifies specific, essential requirements for materials, methods, or practices for use in an unmodified form. May contain discretionary elements.
* Guideline: describes criteria for a general operating practice, procedure, or material for the clinical community. May be modified by the user.
* Report: document that has not been subjected to consensus review
What is the consensus process?
* A voluntary process is a protocol establishing formal criteria for:
o The authorization of a standards project
o The development and open review of documents
o The revision of documents in response to comments by laboratory users
o The acceptance of a document as a clinical laboratory standard
How is consensus reached?
* Consists of formal procedures describing the development of an NCCLS document and criteria for its acceptance as a clinical laboratory standard
* Most NCCLS documents are subject to 2 levels of consensus
o Proposed
o Approved
What are the levels of consensus?
* Proposed: document undergoes the first stage of review.
* Tentative: a tentative standard or guideline made available for review and comment
* Approved: has achieved consensus within the clinical laboratory testing community

How does one design a NCCLS clinical laboratory technical procedure manual?
* Determined by the laboratory’s needs
* Start each procedure on a new page
* Consider using tabs and a table of contents
* Use a numbering system
* Provide supplementary materials where necessary
* Use electronic word-processing equipment

What sources can I use?
* Manufacturer product literature
* Scientific journals
* Textbooks
* Standards publications
* Research and validation data
* Written personal communications

What style must be used in a technical procedure?
* Uniform style
* Month and year adopted
* Page number and total number of pages
* The author and initials of approving authority
* Dated, noted, and signed corrections
* Does it replace a previous procedure

How should I title my procedures?
* Should be concise and descriptive
* Considerations
o The type of specimen
+ Semen Agglutination
o The specific method or instrumentation
+ Mycotrim GM Triphasic Culture System for Identification of Mycoplasma hominis and Ureaplasma urealyticum
o The particular property for which the test procedure is designed
+ Fructose in Seminal Plasma

What is in the principle?
* Includes type of reaction(s), specimen(s), or organism(s) involved
* Clinical reason for performing the test
* Written in paragraph form
* Example:
* Principle: Examine semen specimen for presence of sperm, dead or alive, to evaluate effectiveness of patient vasectomy.

What should be included in specimen collection?
* Specific instructions, such as fasting and special diets, written instructions to the patient that are given for their preparation, and drug regimes that should be noted on the requisition form
* An outline of the steps involved in complicated specimen-collection procedures

Patient Preparation: Patient given written instructions (see Patient Instructions for Semen Collection and Transport of Semen form. (1 of 4)
* Patient Instructions for Collection and Transport of Semen for Laboratory Analysis
* In order to avoid delays and the increased cost of repeat testing, please follow these instruction for preparing for the semen analysis and for properly collecting the semen specimen.
* 1. You must have an appointment in order to have your semen specimen evaluated.
* 2. You must have abstained from (no ejaculation) for a period of 3-5 days (ideally 3 days) before you collect the sample unless otherwise advised by your physician.
* 3. If collected at the laboratory, you will collect in a private room adjacent to the testing area. You may bring your own magazines or videotapes. Check with lab personnel regarding the availability of a VCR.
* 4. If you collect your specimen outside the laboratory collection room, you must
+ keep the sample near body temperature (25°-40°C or 77°-104° F)
+ deliver your sample to the laboratory within 45 minutes of collection

Patient Instructions for Semen Collection and Transport of Semen (2 of 4)
* 5. Collection method
* 6. Preparation for collection

Read more...

Male Obesity and Semen Analysis Parameters



Male Obesity and Semen Analysis Parameters
By:Joseph Petty, MD
Samuel Prien, PhD
Amantia Kennedy, MSIV
Sami Jabara, MD


Background: Obesity
Background: Semen Parameters
* What parameters best predict fertility?
* National Cooperative Reproductive Medicine Network: 765 infertile couples (no conception after 12 months), and 696 fertile couples
* greatest discriminatory power was in the percentage of sperm with normal morphologic features.

Hypothesis
Recent Studies
Sexual function
Hormonal Profile
Interventions: Gastric Bypass
Study Design
* Retrospective chart review for all couples and individual patients presenting for an infertility consultation and evaluation at the Texas Tech Physicians Center for Fertility and Reproductive Surgery from September 2005 through January 2008.
* Intake questionnaire: demographic, medical, surgical and fertility history.
Questionnaire
* Previous pregnancies fathered: current or previous partner

Read more...

Male Infertility



Male Infertility: Definitions
By:Jeanne O’Brien MD
Assistant Professor of Urology and Male Infertility
University of Rochester Medical Center, Department of Urology

Definitions
* Primary infertility: inability to achieve pregnancy > 1yr
* Secondary infertility: previously fertile, now unable >1 yr
* Azoospermia: no sperm in semen
* Oligospermia: reduced sperm concentration <20 million/ml
* Asthenospermia: reduced percent motility <50%
* Teratospermia: reduced percent normal forms <30%
* IVF: in vitro fertilization
* ICSI: intra-cytoplasmic sperm injection

Etiology of Male Infertility
* Varicocele
* Idiopathic
* Infection
* Genetic
* Endocrine
* Immunologic
* Obstruction
* Cryptorchidism

Male Infertility: Evaluation
* Basic Evaluation:
o History (Questionnaire)
o Physical examination
o Standard semen analysis
o Hormonal evaluation
* Optional Additional Evaluation:
o Genetic counseling and evaluation
o Specialized sperm function tests
o Imaging studies
o Testis biopsy

Male Infertility: History
* Duration of infertility
o Previous treatments
o Female-factor (anovulation, tubal obstruction)
* Sexual history
o timing and mechanics of intercourse
o lubricants (peanut oil, olive oil, egg whites ok)

History
* Childhood & Development
o cryptorchidism
o pubertal development
* Medical History
o systemic illness
* Surgical History
o abdominal, pelvic or scrotal surgery
* Infections
o STDs, prostatitis, orchitis (post-pubertal mumps)
* Environmental gonadotoxins
o smoking
o ETOH
o radiation, chemicals, pesticides, chemotherapy
o Heat exposure (short order cook, tanning booths, hot tub/bath)
* Medications (steroids, herbal supplements, hair growth products)

History: Medications
* Hormonal (pre-testicular)
o e.g. androgens, anti-androgens, estrogens
* Gonadotoxic (testicular)
o e.g. chemotherapy/alkylating agents
* Sperm-toxic (post-testicular)
o e.g. Ca-channel blockers

Anatomy of the male reproductive tract

Physical Examination
* General
o Body habitus (muscle mass), hair distribution
o Evidence of normal virilization
* CNS
o visual fields (r/o pituitary adenoma)
o sense of smell (Kallmann’s Syndrome - HypoHypo)
* Abdomen/Pelvis
o Surgical scars
* Genital/Prostate
* Penis:
o length (normal development)
o position of urethral meatus (deposition of semen)
* Prostate :
o size
o firmness
o tenderness
o presence of cysts (ejaculatory duct)
* Testis:
o -position (cryptorchid?)
o -volume (normal ~15-25ml)
o -firmness (normal = firm)

Testis:
o -Seminiferous tubules
+ Germ cells
+ Sertoli cells
o -Interstitium
+ Leydig cells
+ macrophages, endothelial cells
Spermatogenesis
o ~74 days in humans (epididymal transit ~15 days)
o Clinical correlate: Need to wait 3 months after any intervention (medical or surgical) to see a change in semen quality
* Epididymis:
o -fullness
o -cystic changes
* Vas deferens:
o -congenital absence of vas (CAVD)
+ Cystic fibrosis mutations
+ Woolfian duct anomalies

Genital tubercule Penis
Overview of sexual differentiation in the male
(modified from Male Reproductive Biology, eds Lipshultz, Howards)
Varicocele: Diagnosis
* Definition: dilated testicular veins due to reflux of blood
* Established by physical examination (in a warm room)
* Other modalities used to diagnose a sub-clinical varicocele:ultrasound, venography, doppler stethoscope
* However, the subclinical varicocele does not require repair!
* WHO Fertil Steril 1985
* Howards Fertil Steril 1992

Varicocele
* Etiology: probably multi-factorial
Varicocele: Prevalence

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