Body Fluids. Serous fluids Cerebrospinal fluid (CSF)
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Transcript of Body Fluids. Serous fluids Cerebrospinal fluid (CSF)
Body Fluids
Serous fluids
Cerebrospinal fluid (CSF)
Serous fluids
Pleural fluidPericardial fluidPeritonial fluid
Pleural fluid
Pleural fluid
Between visceral and parietal pleura
It is normally about 1-10ml
Mositening the pleural surface
An increased volum is called effusion
Pleural effusion
Definitionthe accumulation of excess fluid within the
pleural space in response to injury ,inflammation, or both
may represent a local response to disease or may just be a manifestation of a systemic illness
Pleural effusion
Rate of Fluid Rate of Fluid
Accumulation Removal
1. Altered Pleural Membrane Permeability2. Decreased Intravascular Oncotic Pressure3. Increased Capillary Hydrostatic Pressure4. Lymphatic Obstruction5. Abnormal Sites of Entry
Clinical Manifestations
PainCoughDyspneaDullness to PercussionDiminished or Absent Vocal ResonanceDiminished or Absent Tactile Vocal FremitusFriction Rub
Radiologic Assessment (1)
Chest X-Ray: PA & Lateral-Decub blunting of either costophrenic angle is indicative of the
accumulation of between 250 - 500 ml of fluid
Lateral-Decubitus films (that allow fluid to shift to the dependent portion of the thoracic cavity) help differentiate fluid from pleural thickening & fibrosis
Radiologic Assessment (2)
Ultrasound: Helpful in Confirming the Presence of a
Small Pleural Effusion & Identifying Loculations
C.T. : Extremely Sensitive !! also helps to view the underlying lung (which may be
obscured by pleural disease) can distinguish between Lung Abscess & Empyema
pp= parietal pleura & Pv=viseral pleura
Pleural Fluid Analysis
1. Gross Appearance2. Cell Count & Differential3. Gm Stain, C & S4. Cytology5. LDH6. Protein7. Glucose, Amylase
Thoracentesis
Thoracentesis ) also known as thoracocentesis or pleural tap) is an invasive procedure to remove fluid or air from the pleural space for diagnostic or therapeutic purposes. A cannula, or hollow needle, is carefully introduced into the thorax, generally after administration of local anesthesia.
A thoracentesis can be diagnostic, which means it is being done to determine the cause of the fluid, for which usually only a syringe of fluid is removed, or it can be a therapeutic thoracentesis, in which the procedure is being done in order to remove as much fluid as possible to relieve symptoms for a patient, with sometimes as much as two liters of effusion fluid being removed.
Pleural effusions do not require Pleural effusions do not require thoracentesis:thoracentesis:
- Underlying congestive heart failure- Underlying congestive heart failure
- After recent thoracic or abdominal - After recent thoracic or abdominal surgery.surgery.
The recommended location varies depending upon the source. It is critical that the patient holds their breath to avoid piercing the lung. Some sources recommend the midaxillary line, in the ninth intercostal space.
ContraindicationsContraindications
Bleeding diathesis,Bleeding diathesis, Systemic anticoagulation,Systemic anticoagulation, Cutaneous infection over site,Cutaneous infection over site, Severe hemodynamic or respiratory Severe hemodynamic or respiratory
compromise,compromise, Mechanical ventilation.Mechanical ventilation.
ComplicationsComplications
Pain at the puncture site,Pain at the puncture site,Cutaneous or internal bleeding, Cutaneous or internal bleeding, Pneumothorax,Pneumothorax,Empyema, Empyema, Spleen/liver puncture.Spleen/liver puncture.
The illustration shows a person having thoracentesis. The person sits upright and leans on a table. Excess fluid from the pleural space
is drained into a bag
Transudate
colorless, clear, odorless fluid with a WBC less than 1000 / mm3
Pleural Membranes are Intact Secondary to Altered Starling Forces Low in Protein & other Large Molecules
CHF, Cirrhosis, Nephrotic Syndrome
Hypoalbuminemia, Constrictive
Pericarditis, SVC Obstruction, Megi syndrome
Exudate
Characterized by Increased Protein & LDH[Pleural Fluid vs. Serum Levels]
Secondary to Disruption of Pleural Membrane or Obstruction of Lymphatic Drainage
Parapneumonic, Infections, Malignancy,
Vasculitic Disease, GI Disease, TB, PE(pulmonary embolism)
Criteria for “Exudative Effusion”
criteria value
1. Pleural Protein : Serum Protein > 0.5
2. Pleural LDH : Serum LDH > 0.6
3. Pleural LDH > 200
only need 1 critical value to establish the diagnosis of exudate
Light’s criteria: Transudate vs. Exudate
Pleural fluid protein / serum protein > 0.5 Pleural fluid LDH / serum LDH > 0.6 Pleural fluid LDH > 2/3 ULN serum LDH
Other criteria: Transudate vs. Exudate
Pleural fluid cholesterol > 45 mg/dL Pleural fluid protein > 3 g/dL
although pleural diseaseitself is rarely fatal, it may be a significant cause of patient morbidity
appropriate treatment may produce
dramatic symptomatic relief !
DIFFERENTIAL DIAGNOSIS Table 57-1
Greater than 10000 per μL--- Parapneumonic effusion, pancreatitis, pulmonary embolism, collagen vascular disease, malignancy, tuberculosis.
Polymorphonuclear ( PMN ) leukocytosis--- Acute disease such as pneumonia, pulmonary embolism, pancreatitis, intra-abdomen abscess, early tuberculosis.
lymphocyte- 100%= Tuberculosis Mononuclear cell--- Malignancy, tuberculosis, resolving acute process. Eosinophil--- Benign asbestos, drug reaction as nitrofurantoin,
bromocriptine, dantrolene, paragonimiasis ( low glucose, low pH, high LDH ) .
Eosinophils >10% caused in about two thirds of cases by blood or air in the pleural
space. More than 50% WBC in exudates are small.
Pleural fluid--- glucose
Glucose typically about the same as blood glucose levels.
Less than 60 mg/dL-Causes: Empyema Malignant effusion Tuberculosis effusion Rheumatoid effusion( usually less than 20)
Pleural fluid--- amylase
Elevated above the upper normal limit of serum amylase---- Esophageal perforation, pancreatic disease, malignancy ( 10% ) .
Acute pancreatitis accompanying pleural effusion--- 10%.
Chronic pancreatic disease may develop a sinus tract between the pancrease and the pleura space.
The amylase associated with malignancy--- salivary type.
Pleural fluid--- lactic acid dehydrogenasePleural fluid lactic acid dehydrogenase---
good indicator of the degree of inflammation in pleural space.
LDH increase, the inflammation worsening.
Pleural fluid--- cytology
Establishing the diagnosis of malignant pleural effusion--- 40-90%.
Depending on--- the tumor type, amount of fluid, skill of cytologist.
Pleural effusion--- bacteriology
Culture and bateriologic stain--- culture both aeobic and anaerobic, mycobacteria, fungi.
Gram’s stain.
Pleural fluid--- pH and pCO2
Less than 7 (empyema) Complicated parapneumonic effusion and tube thoracostomy should instituted.
Less than 7.2--- systemic acidosis, esophageal rupture, rheumatoid pleuritis, tuberculosis pleuritis, malignant pleural disease, hemothorax.
Hemothorax
Blood in the pleural cavity.
Usually results from chest injury.
A blood vessel ruptures into the pleural space or aortic aneurysm leaks blood into the pleural space.
Can occur as a result of bleeding from the ribs, chest wall, pleura, and the lung.
Pleural Fluid Hct
Because a RBC count as low as 5000 cell /mm3, can cause a pleural effusion to turn red, the finding of blood-tinged fluid per se has little
diagnostic value (usually from needle trauma)
A True Hemothorax is when the Pleural Fluid Hct exceeds 50 % of the Peripheral Blood Hct
If Bloody: Hct <1% not significant 1-20% = CA, PE, Trauma >50% serum Hct = hemothorax
Here is an example of bilateral pleural effusions. Note that the fluid appears reddish, because there has been hemorrhage into the effusion.
A bloody pleural effusionoccurring in a patient without a history of
trauma or pulmonary infarctionis
Indicative of Neoplasm in 90 % of cases!
Pleural fluid
Other diagnostic test on pleural fluid---Chylothorax---Triglycerides > 110 mg/dl, Pseudochylothorax--- the level of
cholesterol increase.
Bloody effusion: mesothelioma
Break
Pericardial Fluid
Pericardial Fluid
Surrounding the heart is a sac known as the pericardium, which consists of two membranes. The outer layer being the fibrous parietal pericardium and the inner layer being the serous visceral pericardium. It is the serous visceral pericardium that secretes the pericardial fluid into the pericardial cavity, (the space between the two pericardial layers).
The pericardial fluid reduces friction within the pericardium by lubricating the epicardial surface allowing the membranes to glide over each other with each heart beat
In a healthy individual there is usually 15-50ml of clear, straw-coloured fluid.
However there is little data on the normal composition of pericardial fluid to serve as a reference
Pericardial effusion
A pericardial effusion is the presence of excessive pericardial fluid, this can be confirmed using an echocardiogram
Small effusions are not necessarily dangerous and are commonly caused by infection such as HIV or can occur after cardiac surgery.
Large and rapidly accumulating effusions may cause cardiac tamponade, a life-threatening complication, that puts pressure on the heart preventing the ventricles from filling correctly.
Cardiac tamponade
Cardiac tamponade: the accumulation of fluid in the pericardium in an amount sufficient to cause serious obstruction to the inflow of blood to ventricle results in cardiac tamponade.
The three principal features of tamponade are:
1.elevation of intracardiac pressures
2.limitation of ventricular fillng
3.reduction of cardiac output
The amount of fluid necessary to produce the critical state:Acute tamponade: 150-200 mlChronic tamponade: 1000-2000 ml
The most common causes are:a. neoplastic disease
b. idiopathic pericarditis
c. uremia
d. following cardiac operation
e. trauma
A.clinical features
1. Shortness of breath
2. Weakness and fatigue
3. Anxiety
4. tachycardia
5. Jugular vein engorged
6. Cyanosis
Beck triad:1. increased jugular venous pressure2. hypotension3. diminished heart soundsPulsus paradoxus: A greater than normal (10 mmHg)
inspiratiory decline in systolic arterial pressure.
The CXR of cardiac tamponade:
The echocardiogram of cardiac tamponade:
1. echo free space between epicardium and pericardium
Pericardiocentesis
Pericardiocentesis is a procedure used to remove the pericardial fluid from the pericardial cavity. It is performed using a needle and under the guidance of an ultrasound
It can be used to relieve pressure from pericardial effusions or for diagnostic purposes, revealling the cause of abnormalities such as: Cancer, Cardiac perforation, Cardiac trauma, Congestive
heart failure, Pericarditis rupture of a ventricular aneurysm
Pericardiocentesis
Anesthesia Light sedation will be given to help you relax. You will be awake during the procedure. A
local anesthesia will be injected at the insertion site. It will numb an area on your chest.
Description of Procedure You will lie on a table. An IV line will be inserted into your arm. The sedative will be
delivered this way. The area where the needle will be inserted will be washed. Your heart will be monitored.
The needle will be inserted into the chest. It will be slowly moved toward the heart. Ultrasound and possibly fluoroscopy will be used to help guide the needle to the correct location. The needle will be passed into the pericardial sac, but no further.
Once in the pericardial sac, the fluid will be removed. The needle may be used, or a catheter tube may be inserted over the needle. After some fluid is collected or enough of the fluid has drained out, the needle or catheter will be removed. Pressure will be applied to the injection site for several minutes. This is done to stop the bleeding.
In some cases, your doctor may leave the catheter in place. This will allow draining to continue over several hours or days.
.
Pericardiocentesis needle insertion sites. The subxiphoid and the left sternocostal margin are the most commonly
used sites (black dots)
Immediately After Procedure You will have a chest x-ray to make sure your lung has
not been punctured. You will be closely monitored for several hours after the procedure. Your pulse, blood pressure, and breathing will be checked regularly.
The fluid removed from the pericardial sac is sent to a lab to be analyzed.
How Long Will It Take? About 20-60 minutes How Much Will It Hurt? You may feel pain when the needle is inserted
Average Hospital Stay Hospital stay can vary from one day to
several days. If the catheter remains in place to continue draining fluid, you may need to stay in the hospital several days.
Types
transudative )congestive heart failure, myxoedema, nephrotic syndrome)
Exudative )tuberculosis, spread from empyema)
haemorrhagic )trauma, rupture of aneurysms, malignant effusion(
Malignant) due to fluid accumulation caused by metastasis(
Exudative pericardial effusion developed in over 80% of cases
Presence of antimyocardial Abs suggests an immune mediated process
Hct and RBC count have limited value in differential diagnosis of pericardial effusions.
Total WBC > 10,000/ul suggests bacterial, Tb or malignant pericarditis
Metastatic Ca of lung and breast are most frequent cause of malignant pericardial effusion
Break
Peritonial fluid
Up to 50 ml Fluid normally present in peritoneal cavity
Peritoneal effusion is called AscitesLaboratory criteria for dividing ascitic fluid
into transudate and exudate is not well defined as it is for pleural fluid
Ascites: Physical diagnosis
Bulging flanks
Flank dullness
Shifting dullness
Paracentesis :Indications
New onset ascitesClinical deterioration (fever, pain,
tenderness, mental status change, hypotension)
Suspicion of infection by labs (leukocytosis, acidosis, renal dysfunction)
Alleviation of discomfort/dyspnea
Precautions
Severe coagulopathy or thrombocytopeniaPregnancyOrganomegalyBowel obstructionIntraabdominal adhesionsDistended urinary bladder (Foley first)
Procedure
Identify the patient Obtain consent Perform a “time-out” Identify best site for procedure Sterilize Protect yourself Anesthesia Paracentesis Fluid to the lab for analysis Document procedure and any complications
Technique
Avoid abdominal scars
Midline if possible Midline is avascular Inferior to umbilicus Risk of entering bladder
is low
Semirecumbent position is most commonDullness at site of needle entryUltrasound guidanceMetal needle
1.5 inches 22-gauge for diagnostic paracentesis 16-gauge for therapeutic paracentesis
Disinfect skin with iodine solutionLocal anesthetic for skin and
subcutaneous tissueSterile glovesZ-tractDo not aspirate continuously
Fluid analysis
Cells
Total leukocyte useful in spontaneous bacterial peritonitis (SBP)
Approximately 90% of (SBP) have leukocyte count > 500/ml and over 50% neutrophiles
Eosinophilia > 10% most commonly associates with chronic peritoneal dialysis. Also in CHF, vasculitis, lymphoma and ruptured hydatid cyst
Overall sensitivity of cytology for malignant ascitis is 40-65%
Amylase activity in normal peritoneal fluid is similar to blood levels
A fluid amylase level greater than three times of serum value is good evidence of pancreas-related ascitis and also in GI perforation
Increase CEA in peritoneal washing suggest a poor prognosis of gastric Ca
CA-125 extremely high in epithelial Ca of ovary, follopian tube or endometrium
Other studies of ascitic fluid to be considered
Lactate: An ascites lactate level of >25 mg/dL was found to be 100%
sensitive and specific in predicting active SBP in a retrospective analysis.
pH: In the same study, the combination of an ascites fluid pH of <7.35 and
PMN count of >500 cells/mL was 100% sensitive and 96% specific.
Blood and urine cultures should be obtained in all patients suspected of
having SBP.
Albumin
Is portal hypertension present?SAAG >/= 1.1g/dL
SAAG
Serum-Ascites Albumin Gradient
= serum albumin – ascites albumin> 1.1 = portal hypertension < 1.1 = non-portal hypertension
SAAG classificationSAAG classification
Spontaneous Bacterial Peritonitis (SBP)
Spontaneous bacterial peritonitis (SBP) is an acute bacterial infection of ascitic fluid.
Patients with cirrhosis and ascites carry a 10% annual risk of ascitic fluid infection.
Predisposing factor may be :
Intestinal bacterial overgrowth
Impaired phagocytic function
Low serum and ascites complement levels
Decreased activity of the reticuloendothelial system
Etiologic agents (>90% intestinal flora)
Three forth of infections are due to aerobic gram-negative organisms
(50% of these being Escherichia coli)
One fourth are due to aerobic gram-positive organisms (19%
streptococcal species).
Anaerobic organisms are rare (1%) because of the high oxygen
tension of ascitic fluid.
Clinical presentation and diagnosis of ascitic fluid infection
A broad range of symptoms and signs are seen in SBP. A high index of
suspicion must be maintained when caring for patients with ascites,
particularly those with acute clinical deterioration.
Completely asymptomatic cases in as many as 30% of patients.
Fever and chills occur in as many as 80% of patients.
Abdominal pain or discomfort is found in 70% of patients.
Worsening or unexplained encephalopathy
Diarrhea
Diagnostic paracentesis and direct inoculation of routine blood culture bottles at the bedside with 10 mL of ascitic fluid must be performed.
The results of aerobic and anaerobic bacterial cultures, used in conjunction with the cell count, prove the most useful in guiding therapy for those with SBP.
An ascitic fluid neutrophil count of >500 cells/mL is the single best predictor of
SBP.
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