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  • Parkinson’s Disease

    Parkinson’s Disease: 
    This slowly progressive, degenerative neurologic disorder. This disorder
    is one of the most common crippling disorder in the US.  Deterioration
    progresses for an average of 10 years, at which time secondary disorders
    occurs such as pneumonia, aspiration or some other infection which can
    lead to death.  Parkinson’s disease affects men more often than women.

    Cause:  Uncertain.  Dopamine
    deficiency prevents affected brain cells from performing their normal inhibitory
    function within the central nervous system

    Symptoms:

    Insidious tremor that begins in the fingers (unilateral
    pill roll tremor), increases during stress or anxiety and decreases with
    purposeful movement and sleep

    Muscle rigidity causing resistance to passive
    muscle stretching, which may be uniform or jerky

    Difficulty walking (gait lacks normal parallel
    motion and may be retropulsive or propulsive)

    High-pitched monotone voice

    Drooling

    Masklike facial expression with poor blink reflex
    and wide-open eyes

    Walks with body bent forward (loss of positive
    control)

    Slurred speech

    Oculogyric crises (eyes are fixed upward, with
    involuntary tonic movements)

    Difficulty swallowing (dysphagia)

    Treatment:

    No cure at present

    Treatment seeks to relieve symptoms and keep the
    patient functional as long as possible.

    Drug therapy

    Physical therapy

    Stereotactic neurosurgery

  • Patent Ductus Arteriosus

    Patent: open, unobstructed

    Ductus: fetal blood vessel which joins the aorta and
    pulmonary artery

    Arteriosus:  pertaining to artery

    Patent Ductus Arteriosus:  (PDA)  This
    abnormal opening between the pulmonary artery and the aorta allows left
    to right shunting of blood from the aorta to the pulmonary artery. 
    This results in recirculation of arterial blood through the lungs.

    In the early stages, PDA may produce no clinical effects, but in time
    it can precipitate pulmonary vascular disease, causing symptoms to appear
    by age 40.  The patients with a small shunt or who undergo effective
    surgical repair have a good chance of recovery.  But PDA may advance
    to intractable CHF, which may be fatal.

    Most prevalent in premature infants, PDA often accompanies rubella syndrome. 
    It may be associated with other congenital defects, such as coarctation
    of the aorta, ventricular septal defect, and pulmonary and aortic stenoses.

    Cause:  Results from failure of the fetal ductus arteriosus
    (a fetal blood vessel that connects the pulmonary artery to the descending
    aorta) to close within days to weeks after birth.

    Symptoms:

    For infants, especially premature ones with a large PDA usually develop
    respiratory distress with signs of CHF. 

    Frequent respiratory infections

    Slow motor development

    Failure to thrive.

    Most children with PDA have only cardiac symptoms.  Others may
    exhibit signs of heart disease, such as physical underdevelopment and fatigability.

    By age 40, adults with untreated PDA may develop fatigability and dyspnea
    on exertion.  Cyanosis appears in the final stages of illness.

    Murmur (called Gibson murmur)  This continuous murmur is best heard
    at the base of the heart, at the second left intercostal space under the
    left clavicle in most children with PDA.

    May have bounding peripheral arterial pulses (Corrigan’s pulse), may
    have widened pulse pressure.

    Cardiomegaly

    Tachycardia

    Dilated ascending aorta

    Treatment:

    For infants with PDA that has no symptoms (asymptomatic) the patient
    may not require immediate treatment.

    Those with CHF require fluid restriction, diuretic, and digitalis to
    minimize or control symptoms.  If theses measure does not control
    CHF, the patient requires surgery to ligate the ductus.  The doctor
    may delay surgical correction until age 1 if the patient has only mild
    symptoms.

    Before surgery, children with PDA require antibiotics to protect against
    infective endocarditis.

    Other forms of therapy include cardiac catheterization to deposit a
    plug in the ductus to stop shunting, or administration of indomethacin
    I.V. (a prostaglandin inhibitor that provides an alternative to surgery
    in premature infants) to induce ductus spasm and closure.

  • Pharyngitis

    Pharyngitis:  Inflammation of the pharynx, referred
    to also as sore throat.

    Pharyngitis can be acute or chronic inflammation.  Commonly among
    adults who live or work in dusty or very dry environments, use their voices
    excessively, use tobacco or alcohol habitually, or suffer from chronic
    sinusitis, persistent coughs, or allergies.

    Acute pharyngitis may precede the common cold or other communicable
    diseases.  Chronic pharyngitis is commonly an extension of nasopharyngeal
    obstruction or inflammation.  Uncomplicated pharyngitis usually subsides
    in 3 to 10 days.

    Cause;  In children, it is often caused by streptococcal bacteria. 
    In 90% of cases, pharyngitis occurs as the result of a virus.

    Symptoms:

    Sore throat

    Difficulty swallowing (swallowing saliva is usually more painful than
    swallowing food)

    Sensation of a lump in the throat

    Have the urge to swallow constantly

    Redden, inflamed posterior pharyngeal wall

    Mild fever

    Headache

    Muscle and joint pain – especially in bacterial pharyngitis

    Treatment:

    Treatment is usually symptomatic – consisting mainly of rest, warm saline
    gargles, throat lozenges containing a mild anesthetic, plenty of fluids,
    and analgesics as prescribed by your doctor.

    Bacterial pharyngitis requires antibiotic therapy – usually penicillin
    or another broad spectrum antibiotic if the patients is allergic to penicillin.

  • Pneumonia

    Pneumonia:  is an inflammation of the alveoli and may
    be caused by a diplococcus known as the pneumococcus, although pneumonia
    can also be caused by a streptococcus, a staphylococcus or a virus as well
    as chlamydias.  Any or all of these pathogens may be carried by a
    healthy person in the mucosa of the upper respiratory tract.  If the
    person remains in good condition, these pathogens may be carried for an
    indefinite period with no ill effect.  However, if the individual’s
    resistance to infection is lowered, the pathogens then may invade the tissues
    and work their damage.  Exposure to inclement weather for long periods
    of time, alcoholism, malnutrition, a severe injury or other debilitating
    or weakening conditions may cause a susceptibility to pneumonia.

    There are two main kinds of pneumonia as determined by the method of
    lung involvement and other factors.  These are:

    1.) Lobar pneumonia, in which an entire lobe of the lung
    is infected at one time.  The organism is usually a pneumoncoccus,
    although other pathogens also may cause this disease.

    2.) Bronchopneumonia, in which the disease process is
    scattered here and there throughout the lung.  The cause may be a
    staphylococcus, a gram -negative proteus or colon bacillus (not normally
    pathogenic), or a virus.  Bronchopneumonia most often is secondary
    to an infection or to some agent which has lowered the individual’s resistance
    to disease.  This is the more common form of pneumonia.

    Lobar pneumonia may develop suddenly in an apparently well individual,
    often in a fairly young hale-appearing male.  Bronchopneumonia, on
    the other hand, is much more  common in the very young and the very
    old. 

    Symptoms:

    Coughing

    Sputum production ( may have red streaks in the sputum due to some red
    blood cells may be present)

    Pleuritic chest pain

    Chills

    Fever

    Lack of oxygen 

    Treatment:

    Antimicrobial therapy (varies with the infecting agent)

    You get a pneumococcal polysaccharide vaccine to protect against the
    most common form of pneumonia.

    Oxygen therapy

    May require mechanical ventilation for respiratory failure

    High Calorie diet and adequate fluid intake

    Bed rest

    Analgesic to relieve pleuritic chest pain as doctor order

    Antibiotic drugs have greatly improved the outlook for pneumonia patients.

    Also
    See Our Page On;
      Flu / Pneumonia / and Food Poisoning 
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  • Polycystic Kidney Disease

    Polycystic Kidney Disease: 
    Characterized by multiple, bilateral, grape-like clusters of fluid filled
    cysts that grossly enlarge the kidneys, compressing and eventually replacing
    functioning renal tissue.  This disorder is inherited.  It appears
    in two distinct forms.  The infantile form causes stillbirth or early
    neonatal death.  Infants with this disease may survive for 2 years
    and then develop fatal renal, congestive heart, or respiratory failure. 
    Onset of the adult form is insidious but commonly becomes obvious between
    ages 30 and 50.  Rarely, polycystic kidney disease doesn’t cause symptoms
    during an individual’s life-time, and may only be found during autopsy. 
    Renal deterioration in the adult form of this disorder is slower than in
    the infantile form, but often leads to renal failure.

    Cause:  The infantile form appears
    to be inherited as an autosomal recessive trait.  The adult form appears
    to be autosomal dominant trait.

    Symptoms:

    Infantile: 

    Pronounced epicanthal folds (a vertical fold
    of skin on either side of the nose)


    Pointed nose

    Small chin

    Floppy, low set ears

    Huge bilateral masses on the flanks. 

    Enlarged kidney

    Adult : 

    Hypertension 

    Polyuria 

    Signs and symptoms of urinary tract infection 

    Lumbar pain 

    Widening girth, and swollen or tender abdomen 

    Hematuria 

    Life threatening retroperitoneal bleeding 

    Proteinuria 

    Colicky abdominal pain

    Enlarged kidney

    Diagnostic test:

    Retrograde pyelography reveals enlarged kidneys,
    with elongation of the pelvis, flattening of the calyces, and indentations
    caused by cysts.

    IVP: neonate shows poor excretion of contrast
    medium

    CT scan and ultrasound show kidney enlargement
    and the presence of cysts

    Urinalysis and creatinine clearance tests indicate
    abnormalities.

    Treatment:

    Goal:  to preserve the renal parenchyma and
    avoid infection.

    No known cure.  Careful management of associated
    urinary  tract infections and secondary hypertension may prolong life.

    Antibiotic therapy 

    Dialysis or kidney transplantation.

  • Prostate Problems

    Prostatitis:  Inflammation
    of the prostate gland.  This disorder may be acute or chronic. 
    Acute prostatitis most often results from gram-negative bacteria and is
    easy to  recognize and treat.  Chronic prostatitis, the most
    common cause of recurrent Urinary Tract Infection in men, isn’t easily
    recognizable.

    Cause:  Primarily from infection
    by Escherichia coli.  It also results from infection by Klebsiella,
    Enterobacter, Proteus, Pseudomonas, Streptococcus, or Staphylococcus.

    Symptoms:

    Acute prostatitis:  Sudden fever, chills,
    low back pain, myalgia, perineal fullness, arthralgia,  urinary urgency,
    possibly painful urination, nocturia, cloudy urine.  Rectal palpation
    of the prostate reveals marked tenderness, induration, swelling, firmness,
    and warmth.

    Chronic prostatitis:  may present no symptoms. 
    Usually having the same symptoms as an acute prostatitis, but is less severe.


    Other symptoms may include:  painful ejaculation,
    hemospermia, persistent urethral discharge, and sexual dysfunction

    Treatment:

    Systemic antibiotic therapy

    Chronic prostatitis usually requires a long term
    course of treatment


    Epididymitis:  Infection of
    the epididymis.  The cordlike excretory duct of the testis, is one
    of the most common infections of the male reproductive tract.  Usually,
    the causative organisms spread from established UTI or prostatitis and
    reach the epididymis through the lumen of the vas deferens.  Rarely,
    epididymitis is secondary to a distant infection, such as pharyngitis or
    tuberculosis, that spreads through the lymphatic system or, less commonly,
    the bloodstream.  Epididymitis may spread to the testis itself.

    Cause:  Usually results from
    pyogenci organisms, such as staphylococci, Escherichia coli, and streptococci. 
    Other causes include:  gonorrhea, syphilis, chlamydial infection,
    trauma, prostatectomy, and chemical irritation resulting form extravasation
    of urine through the vas deferens.

    Symptoms:

    Pain

    Extreme tenderness

    Swelling in the groin and scrotum

    High fever

    Malaise

    Treatment:

    Broad spectrum antibiotic

    Analgesics

    Ice bag may be applied to the area to reduce swelling
    and relieve pain

    Bedrest may be needed

    In older patient undergoing open prostatectomy,
    bilateral vasectomy may be necessary to prevent epididymitis as a postoperative
    complication.  When epidymitis is refractory to antibiotic, epididymectomy
    under local anesthesia is necessary.

    Corticosteroids may be prescribed to help counteract
    inflammation (but their use is controversial)

  • Prostatic Cancer

    Prostatic Cancer:  Is the
    second most common cancer in men over age 50.  Incidence is highest
    among blacks and in men with blood type A, and lowest in Asians. 
    It is important that all males over age 40 should undergo a rectal examination
    as part of their annual physical examination.

    Cause:  Unknown

    Symptoms:

    Usually signs and symptoms of prostatic cancer
    appear in the advanced stages of the disease.

    Difficulty urinating

    Urine dribbling

    Urine retention

    Unexplained cystitis and hematuria

    A hard nodule may appear on rectal examination
    (this may be felt before symptoms develop.

    Treatment:

    Varies with each stage of the disease but generally
    include:

    Radiation

    Prostatectomy

    Orchiectomy (to decrease androgen production)

    Hormone therapy

  • Psoriasis

    Psoriasis:  This chronic disorder is marked by epidermal
    proliferation and recurring remissions and exacerbation’s.  It’s lesions,
    which appear as red ( erythematous papules ), and plaques covered with
    silvery scales, vary widely in severity and distribution.  The tendency
    to develop psoriasis is genetically determined.  Studies shows significantly
    higher than normal incidence of human leukocyte antigen (HLA) in patients
    with psoriasis, suggesting a possible autoimmune deficiency.

    Symptoms: 

    Small erythematous papules

    Red, elevated plaques with silver scales appearing on the scalp, face,
    chest, elbows, knees, back, buttocks, genitals.

    Itching (pruritus)

    Possible nail pitting and joint stiffness

    Treatment :

    No permanent cure exists

    Intervention varies:  * lukewarm baths and the application of
    occlusive ointment bases (petrolatum or preparation containing urea)

     * Salicylic acid preparations – it may soften and remove psoriatic
    scales

     * Steroid creams such as Hydrocortisone cream/oint.

     * Ultraviolet light – wavelength B (UVB) or natural sunlight
    (methods to retard rapid cell proliferation to the point of minimal erythema)

     * Anthralin, combined with a pasted mixture may be prescribed
    for well defined plaques but mustn’t be applied to unaffected areas, because
    it may cause inflammation.  Anthralin irritates and stains the skin. 
    It also stains clothing and household items, such as the sink or bathtub.

    In patient with severe chronic psoriasis treatment includes:

     * Goeckerman treatment – which combines tar application and UVB
    – It may achieve remission and clear the skin.

     * Ingram technique – a variation of this treatment, uses anthralin
    instead of tar.

     * A program called PUVA (Photo – therapy) – combines administration
    of methoxsalen (a psoralen derivative) with exposure to ultraviolet light,
    wavelength A.

     * Methotrexate – may help severe, refractory psoriasis

     * For last resort, the doctor may prescribe etretinate therapy.

    To relieve pruritus – low dose of antihistamines, oatmeal baths, emollients
    (perhaps with phenol and methol), and open dressings.

    To alleviate the pain of psoriatic arthritis – aspirin and local heat
    application

    For severe cases – may require nonsteroidal anti – inflammatory drugs

    Treatment for psoriasis of the scalp usually consists of a tar shampoo,
    followed by an application of a steroid lotion while the hair is still
    wet.

    No effective treatment exists for psoriasis of the nails, the nails
    usually improve as skin lesions improve

  • Pyelonephritis

    Acute pyelonephritis or kidney infection: 
    One of the most common renal diseases.  Pyelonephritis most commonly
    results from an ascending infection.  The most common infecting organism
    is Escherichia coli.  Others are Proteus, Pseudomonas, Staphylococcus
    aureus, and Streptococcus faecalis.  It primarily affects the interstitial
    area and the renal pelvis and, less often, the renal tubules.  Risk
    factors can include diagnostic and therapeutic use of instruments, as in
    catheterization, cystoscopy, or urologic surgery.  Inability to empty
    the bladder, urine stasis (stoppage), urinary obstruction from tumors,
    strictures, or benign prostatic hypertrophy can also lead to pyelonephritis. 
    Other risk factors includes; sexual activity in women (intercourse increases
    the risk of bacterial contamination), pregnancy – approx. 5% of pregnant
    women develop asymptomatic bacteriuria, if left untreated, about 40% 
    develop pyelonephritis.  diabetes are also prone to develop pyelonephritis
    (glycosuria may support bacterial growth in the urine) 

    Symptoms: 

    Urinary urgency

    urinary frequency

    Burning during urination

    Dysuria (difficulty and or painful urination)

    Nocturia (excessive urination at night)

    Hematuria (blood in the urine) usually microscopic but possibly gross
    (visible)

    Possible cloudy urine

    urine may have a foul smell – fishy odor

    Fever of 102 degrees or higher

    Chills, shaking chills

    Flank pain

    Anorexia

    Fatigue

    Treatment:

    Antibiotic therapy for specific infecting organism.

    If the infecting organism can’t be identified, treatment consist of
    a broad – spectrum antibiotic.

  • Q Fever

    Q Fever: Is a infectious disease
    caused by an organism called Coxiella Burnetii. This type of bacteria usually
    lives in domestic animal such as; cows, goats and sheep. It can also
    be found with wild animals, dogs, cats and ticks. Q Fever can cause
    Pneumonia and Hepatitis. Q Fever is found more in people who works with
    live stocks, farm workers and Veterinarians, who come in contact with blood,
    tissues and feces of infected animals. It is found in unpasteurized milk
    from infected cow and or goats. It can also be found in soil that has been
    contaminated with this bacteria.

    Symptoms:

    * symptoms usually develops 72 hours after coming in contact
    with the bacteria and up to 30 days later

    Flu like symptoms such as; fever, chills, muscle and joint pains

    Dry cough

    Chest pain

    Abdominal pain

    May show signs of hepatitis (jaudance)

    If untreated, the patient can develop complications such as:

    Endocarditis

    Encephalitis

    Chronic Hepatitis

    Osteomylelitis

    Treatment:

    Controlling the symptoms and the use of Antimicrobials

    Your doctor will probably do lab work, and or chest X-ray

    * Call your doctor if you think you may have been exposed to
    the bacteria ( Coxiella Burnetii ) Promptly.