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Morning Report - 2
November 3, 2016
Khushboo Gandhi, PGY2
Internal Medicine, St. Luke’s Hospital
33 year old CF
presents with
nausea,
vomiting and
diarrhea.
HPI: 09/23/2016 4:50 PM
She was in her usual state of health until 2 pm today.
She works as a school bus driver for special needs
children and while she was driving the bus, she began to
feel very nauseated and had to pull over. She then
began to vomit and have diarrhea. 5 times each
She had lunch which consisted of tuna noodle casserole
at around noon.
Review of Systems in ED:
Constitutional: Weakness, No fever, No chills, No fatigue, No decreased activity, No loss of appetite, No
weight gain.
Eye: No recent visual problem, No double vision.
Ear/Nose/Mouth/Throat: No decreased hearing, No ear pain, No nasal congestion, No sore throat.
Respiratory: no shortness of breath, no cough, no sputum production, No hemoptysis.
Cardiovascular: Tachycardia, No palpitations, No peripheral edema, no chest pain
Gastrointestinal: Nausea, Vomiting, Diarrhea, No constipation, No abdominal pain.
Genitourinary: No dysuria, No change in urine stream.
Hematology/Lymphatics: No swollen lymph glands.
Endocrine: No excessive thirst.
Immunologic: Not immunocompromised.
Musculoskeletal: No neck pain, No joint pain, No decreased range of motion.
Integumentary: No rash, No pruritus, No petechiae, No skin lesion.
Neurologic: Alert and oriented X4, No confusion, No numbness, No tingling, No headache.
Psychiatric: Anxiety, Depression.
PMH/PSH:
End stage renal disease secondary to heavy NSAID use + Reflux nephropathy (Recurrent UTI with
pyelonephritis) (Took 55 tabs of Aleve in one day to relieve abdominal pain secondary to IUD in 2002) ---
s/p CAPD since July 2016, Last dialysis at 11 AM today, due to start on cycler tonight first time
Asthma/chronic bronchitis -- well controlled with albuterol inhaler as needed. No history of intubations
secondary to asthma. Hospitalized once due to asthma , a year ago.
Chronic migraines
Depression, Anxiety
Gout
Cholecystectomy, AV fistula creation x2 (was on HD for 3 weeks prior to PD but discontinued due to
work schedule), Kidney stent, Peritoneal dialysis catheter insertion, Tonsillectomy, Mirena IUD insertion
Allergies:
Advil- Renal failure.
Aleve- Renal failure.
Amoxicillin- Stopped breathing.
Dilaudid- Itching, breathing problems.
Levaquin- Stopped breathing.
Morphine- hives; Vicodin ok
Penicillin- Stopped breathing.
Family History:
Mother - DM - Insulin controlled, Thyroid cancer
Social History:
She is divorced and lives alone with her daughter. She works as a bus driver for special needs children.
Former smoker, quit in 2004, smoked 10 cigs/day for 2 years, No alcohol intake, no drug abuse.
Meds:
Albuterol: 2 puffs, Inhalation, q4hrs, PRN (shortness of breath)
Aspirin: 81 mg, 1 tablet, Oral, daily
Cholecalciferol: 2,000 units, Oral, daily
Sertraline: 100 mg, Oral, bid
Physical Examination in ED 8:30 PM:
Vitals: TMax: 36.9; HR: 126 regular; RR: 20; SpO2: 98 % on RA BP: 128/95 mm hg.
Height: 152.4 cm Weight: 76.4 kg BMI:32.89
General: Alert and oriented, no acute distress
Skin: Normal for ethnicity, No edema, Not pale.
HENT: Normocephalic, Oral mucosa is moist, No pharyngeal erythema.
Eye: Pupils are equal, round and reactive to light, Normal conjunctiva.
Neck: Supple, No carotid bruit, No jugular venous distention, No lymphadenopathy.
Respiratory: No chest wall tenderness, lungs are clear to auscultation, respirations are nonlabored
Cardiovascular: Regular rhythm, No murmur, Tachycardia, Good pulses equal in all extremities, No edema.
Gastrointestinal: Soft, Non-tender, Normal bowel sounds.
Lymphatics: No lymphadenopathy neck, axilla, groin.
Musculoskeletal: Normal range of motion, Normal strength, No swelling.
Integumentary: Warm, Dry, Pink.
Neurologic: Alert, Oriented, No focal defects.
Psychiatric: Cooperative, Appropriate mood & affect.
Genitourinary: No Costovertebral Angle tenderness.
HPI continues…
After arriving on floor,
Nurse notifies NP on the floor that patient had become very short of breath and wheezing
Review of Systems on floor at 11:37 PM:
Constitutional: Weakness, No fever, No chills, No fatigue, No decreased activity, No loss of appetite, No
weight gain.
Eye: No recent visual problem, No double vision.
Ear/Nose/Mouth/Throat: No decreased hearing, No ear pain, No nasal congestion, No sore throat.
Respiratory: Shortness of breath, Cough, Wheezing, No hemoptysis.
Cardiovascular: Tachycardia, No palpitations, No peripheral edema. Chest pain: Midsternal, Anterior.
Gastrointestinal: Nausea, Vomiting, Diarrhea, No constipation, No abdominal pain.
Genitourinary: No dysuria, No change in urine stream.
Hematology/Lymphatics: No swollen lymph glands.
Endocrine: No excessive thirst.
Immunologic: Not immunocompromised.
Musculoskeletal: No neck pain, No joint pain, No decreased range of motion.
Integumentary: No rash, No pruritus, No petechiae, No skin lesion.
Neurologic: Alert and oriented X4, No confusion, No numbness, No tingling, No headache.
Psychiatric: Anxiety, Depression.
Physical Examination on floor at 11:27 PM:
Vitals: TMax: 36.9; HR: 104 regular; RR: 32; SpO2: 94 % on 2 L/m BP: 127/94 mm hg.
Height: 152.4 cm Weight: 76.4 kg BMI:32.89
General: Alert and oriented, Severe distress, not able to complete full sentences.
Skin: Normal for ethnicity, No edema, Not pale.
HENT: Normocephalic, Oral mucosa is moist, No pharyngeal erythema.
Eye: Pupils are equal, round and reactive to light, Normal conjunctiva.
Neck: Supple, No carotid bruit, No jugular venous distention, No lymphadenopathy.
Respiratory: No chest wall tenderness.
Respiratory rate: 30 breaths/minute, Tachypneic. Pattern: Regular.
Breath sounds: Right, Upper lobe, Lower lobe, Diminished, Expiratory wheezes, No crackles present.
Right lower lung dull to percussion
Cardiovascular: Regular rhythm, No murmur, Tachycardia, Good pulses equal in all extremities, No edema.
Gastrointestinal: Soft, Non-tender, Normal bowel sounds.
Lymphatics: No lymphadenopathy neck, axilla, groin.
Musculoskeletal: Normal range of motion, Normal strength, No swelling.
Integumentary: Warm, Dry, Pink.
Neurologic: Alert, Oriented, No focal defects.
Psychiatric: Cooperative, Appropriate mood & affect.
Genitourinary: No Costovertebral Angle tenderness.
CBC 09/23 09/24
WBC 8.7 H 11.4
RBC 4.43 4.21
Hemoglobin 13.1 12.3
Hematocrit 40.4 39.2
MCV 91.2 93.1
MCH 29.6 29.2
MCHC 32.4 L 31.4
RDW 13.3 13.5
MPV 10.8 10.6
Platelets 246 223
Diff 09/23 09/24
Neutro % 0.2 0.4
Lymph % 63 91
Mono % 28 5
Eos % 8 4
Baso % 1 0
Immature Gran
%
0 0
Neutro # 5.5 H 10.3
Lymph # 2.4 L 0.5
Mono # 0.7 0.5
Eos # 0.1 0.0
Baso # 0.0 0.0
Sed rate 28
General Chemistry 09/23 09/24
Sodium 140 144
Potassium 3.9 f C 2.8
Chloride 102 104
Co2 26 L 17
Anion Gap 12 H 23
BUN H 23 H 20
Creatinine H 5.8 H 5.6
Glucose 95 H 246
Calcium 8.8 8.5
Protein, Total 7.2
Albumin 4.2
Alk Phos 79
Bilirubin, Total 0.7
AST 28
ALT 25
Phosphorus
eGFR L 8 L 9
eCrCl f 0.2 f 0.2
LD 416
Magnesium H 2.6
Labs:
Blood Gases 09/24 09/24
pH 7.40 L 7.33
pCo2 37 33
pO2 L 58 87
HCO3 23 L 17
O2 Sat L 91 97
L/min 2 3
Urine Analysis
UA Color Straw
UA Clarity Clear
UA SG 1.005
UA pH 7.0
UA LE A 1+
UA Nitrite Negative
UA Protein A 2+
UA Protein (Qual) A Trace
UA Glucose (Qual) Negative
UA Ketones Negative
UA Urobilinogen Negative
UA Bilirubin A Trace
UA Blood A 6-10
UA WBC <3
UA RBC A Rare
UA Bacteria A Moderate
Blood Culture Negative
Blood Culture Negative
Urine Culture Negative
Influenza Negative
Res. PCR Negative
Nasal MRSA Negative
Development of a moderate right pleural effusion with right basilar atelectasis and/or infiltrate.
Overnight patient became extremely short of breath, unable to complete full sentences and was
transferred to ICU in the morning following this x-ray finding
Fluid Analysis
Nucleated Cells f <50
RBC 2,000
Glucose f 497
LD f 222
Protein f <2.0
Hospital Course:
Pt was started on peritoneal dialysis cycler on the night of admission and developed acute respiratory distress due to
severe right pleural effusion.
Patient was transferred to ICU, peritoneal dialysis was stopped and right thoracentesis was performed, with drainage of
3.2 L of fluid.
Fluid analysis was consistent with 1.5% Dianeal concentration PD solution.
Hydrothorax/Pleural effusion due to peritoneo-pleural leak.
IV antibiotics for possible pneumonia with aztreonam and vancomycin
Did receive Duonebs and steroid for one day due to concern for Asthma exacerbation
CT chest next day showed infiltrate in right upper lobe - Reexpansion edema
Vancomycin was discontinued and continued on aztreonam
She was started on hemodialysis and discharged home on 9/28/2016
09/25 CT CHEST W/O CONTRAST
● Moderately large right pleural effusion.
● Trace left pleural effusion present.
● Infiltrate in the right upper lobe.
● Partial consolidation and atelectasis noted in
the right middle lobe and right lower lobe.
● Left basilar infiltrate and atelectasis noted.
● 0.2 m noncalcified nodule
“Sweet Hydrothorax”
Acute Hydrothorax Complicating
Peritoneal Dialysis
PLEURAL EFFUSION DUE TO PLEUROPERITONEAL LEAK:
Hydrothorax associated with abnormal communications between the pleura and peritoneal cavities
was first described by Meigs, who reported the coexistence of pleural effusion and ascites
associated with ovarian fibroma
Typically occurs early in the course of PD
Not related to the volume of instilled dialysate
Source of the leak - Congenital or acquired communications between the pleura and the peritoneum
Diaphragmatic hernias allow dissection of fluid through defects around the major vessels and the
esophagus or through diaphragmatic foramina
Negative intrathoracic pressure, combined with an increased intra-abdominal pressure caused by
dialysate instillation, may open small defects in the diaphragm - promote the flow of dialysate into
the pleural space.
Acquired diaphragmatic defects - eight years after starting peritoneal dialysis
Epidemiology:
Incidence is 1.6 to 10 percent
largest study reported to date - 50 of 3195 patients (1.6 percent) developed acute hydrothorax after
starting peritoneal dialysis
Women are affected more commonly than men
Patients with polycystic kidney disease are predisposed to develop pleuroperitoneal leaks -
Significantly reduced abdominal capacity
Marked increase in hydrostatic pressure after the infusion of dialysate
Peritonitis increases the incidence of hydrothorax - 6% suffered peritonitis
Clinical characteristics:
Dyspnea and inadequate ultrafiltration ability
Asymptomatic (26 percent)
Right side - 50 to 90 percent of cases
Most appear early after the initiation of peritoneal dialysis
50% - within 30 days of starting PD
20% - after one year
Diagnosis:
Dyspneic nonedematous patient
Ultrafiltration is consistently inadequate
Modalities for the diagnosis of abdominal and thoracic cavity defects in peritoneal dialysis patients
PERITONEAL SCINTIGRAPHY
Safe, accurate, and rapid way of diagnosing leaks in the peritoneal cavity.
3 to 5 millicuries of technetium 99m isotope per 0.5 to 2.0 L of dialysis solution is injected into the
abdominal cavity.
Multiple projections (anterior, lateral, posterior, and oblique) are then taken to help diagnose leaks,
hernias, and hydrothorax
Although a significant dose of isotope is used, it is not absorbed from the peritoneum, and almost all
of the material drains out of the body after the procedure.
The net dose of radiation is therefore only a fraction of the total dose instilled into the peritoneal
cavity
CT SCANS AND CT PERITONEOGRAPHY
Accurate and reliable methods of diagnosing peritoneal defects.
CTP Vs CTS - small leaks, adhesions, loculated fluid collections, intraabdominal abscesses, and
pseudocysts
The dose of iodinated contrast - 50 mL per liter of dialysis fluid.
Oral and intravenous (IV) contrast can be simultaneously given to diagnose any abscesses or tumors
CTP is not effective in diagnosing obstruction of the catheter by fibrinous, adhesions or omentum
Recommend CTP as the initial diagnostic modality to be utilized.
Cumulative radiation exposure may be of concern in pediatric populations.
MRI AND MR PERITONEOGRAPHY
Gadolinium based dye
Moderate to advanced renal failure (dialysis dependent or eGFR <30 mL/min) - severe syndrome of
nephrogenic systemic fibrosis.
CLINICAL METHODS:
Easy to perform, but not sensitive enough to diagnose these defects
Thoracentesis
Especially helpful in patients who are acutely symptomatic
Diagnostic as well as therapeutic.
Dialysate fluid in the pleura should have a higher concentration of glucose than plasma (50 mg/dl)
Concentrations of lactate dehydrogenase (LDH) and protein are consistent with a transudate
Cell count and cultures (to exclude infection)
L and D isomers of lactate - L isomer of lactate is endogenous
Commercial dialysis solutions have both L and D isomers
Methylene blue dye — Instillation of methylene blue dye into the peritoneum - useful in diagnosing
leaks. Some case reports of irritation to the abdominal viscera
Clinical observation — An easier, but relatively insensitive method of diagnosing hydrothorax.
keep the abdomen dry overnight and to repeat a chest radiograph in the morning to determine if the
pleural effusion has decreased
Management:
Depends upon the acuity and severity of the patient's symptoms and desire to continue with
peritoneal dialysis as a treatment modality
Acute thoracentesis to remove large pleural effusions is rarely required
Most cases - draining the peritoneal cavity and avoiding overnight (supine) dwells is sufficient
If the leak is small and the patient has adequate residual function to permit intermittent dialysis (eg,
nocturnal peritoneal dialysis) - PD can be continued.
Continued - if estimated duration of dialysis is short, such as the patient who will soon undergo a
living, related transplant
Some pleuroperitoneal leaks spontaneously resolve (after temporary transfer to hemodialysis) - Cure
rate is only 40 percent with conservative therapy
Chemical pleurodesis - Recurrent pleural effusion, unresponsive to conservative measures, who
needs and/or desires to continue with peritoneal dialysis
In one review, pleural effusion resolved after pleurodesis in 67 percent of patients
Agents - Autologous blood, talc, and tetracycline
Temporary cessation of CAPD - first-line treatment
Video-assisted thoracoscopic pleurodesis or repair - who failed conservative management
Surgical correction of an identified diaphragmatic defect - Thoracotomy
Most patients with pleuroperitoneal leaks ultimately require permanent transfer to hemodialysis
Noninfectious complications of continuous peritoneal dialysis
Continuous ambulatory peritoneal dialysis [CAPD] and Continuous cycler peritoneal dialysis [CCPD]
Due to increased intra abdominal pressure resulting from instillation of dialysate into the peritoneal
cavity
Hernia formation
Leaks (including hydrothorax or pleuroperitoneal leaks)
Local edema
Back pain
GI problems: gastroesophageal reflux, delayed gastric emptying
Not related to increased intra abdominal pressure
Hemoperitoneum
Pain on infusion of dialysate
Electrolyte imbalances
Ultrafiltration failure
GERD - Increased intraabdominal pressure on lower esophageal sphincter
Delayed gastric emptying - mechanical or neurogenic mechanism triggered by the presence of intra-
abdominal fluid retards gastric emptying - metoclopramide/erythromycin
Back pain - Increased mechanical stress on the lumbar spine - due to the tendency of patients to
assume a more lordotic position because of increased intraabdominal pressure
PAIN ON DIALYSATE INFUSION — Abdominal pain often occurs with infusion of dialysate into the
peritoneal cavity even in the absence of peritonitis.
Acidic pH (pH 5.2 to 5.5) of conventional lactate dialysate.
Poor catheter position
Dialysate temperature
High glucose concentration of hypertonic dialysis solutions
Rx - May be treated with intraperitoneal infusion of bicarbonate/local anesthetic - Risk of contamination
and peritonitis; Slowing the rate of infusion; Catheter replacement
Electrolyte abnormalities:
Hypokalemia and hypermagnesemia
liberalization of dietary potassium and, often, oral potassium supplementation may be needed.

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Morning report 2 november 3, 2016

  • 1. Morning Report - 2 November 3, 2016 Khushboo Gandhi, PGY2 Internal Medicine, St. Luke’s Hospital
  • 2. 33 year old CF presents with nausea, vomiting and diarrhea. HPI: 09/23/2016 4:50 PM She was in her usual state of health until 2 pm today. She works as a school bus driver for special needs children and while she was driving the bus, she began to feel very nauseated and had to pull over. She then began to vomit and have diarrhea. 5 times each She had lunch which consisted of tuna noodle casserole at around noon.
  • 3. Review of Systems in ED: Constitutional: Weakness, No fever, No chills, No fatigue, No decreased activity, No loss of appetite, No weight gain. Eye: No recent visual problem, No double vision. Ear/Nose/Mouth/Throat: No decreased hearing, No ear pain, No nasal congestion, No sore throat. Respiratory: no shortness of breath, no cough, no sputum production, No hemoptysis. Cardiovascular: Tachycardia, No palpitations, No peripheral edema, no chest pain Gastrointestinal: Nausea, Vomiting, Diarrhea, No constipation, No abdominal pain. Genitourinary: No dysuria, No change in urine stream. Hematology/Lymphatics: No swollen lymph glands. Endocrine: No excessive thirst. Immunologic: Not immunocompromised. Musculoskeletal: No neck pain, No joint pain, No decreased range of motion. Integumentary: No rash, No pruritus, No petechiae, No skin lesion. Neurologic: Alert and oriented X4, No confusion, No numbness, No tingling, No headache. Psychiatric: Anxiety, Depression.
  • 4. PMH/PSH: End stage renal disease secondary to heavy NSAID use + Reflux nephropathy (Recurrent UTI with pyelonephritis) (Took 55 tabs of Aleve in one day to relieve abdominal pain secondary to IUD in 2002) --- s/p CAPD since July 2016, Last dialysis at 11 AM today, due to start on cycler tonight first time Asthma/chronic bronchitis -- well controlled with albuterol inhaler as needed. No history of intubations secondary to asthma. Hospitalized once due to asthma , a year ago. Chronic migraines Depression, Anxiety Gout Cholecystectomy, AV fistula creation x2 (was on HD for 3 weeks prior to PD but discontinued due to work schedule), Kidney stent, Peritoneal dialysis catheter insertion, Tonsillectomy, Mirena IUD insertion Allergies: Advil- Renal failure. Aleve- Renal failure. Amoxicillin- Stopped breathing. Dilaudid- Itching, breathing problems. Levaquin- Stopped breathing. Morphine- hives; Vicodin ok Penicillin- Stopped breathing.
  • 5. Family History: Mother - DM - Insulin controlled, Thyroid cancer Social History: She is divorced and lives alone with her daughter. She works as a bus driver for special needs children. Former smoker, quit in 2004, smoked 10 cigs/day for 2 years, No alcohol intake, no drug abuse. Meds: Albuterol: 2 puffs, Inhalation, q4hrs, PRN (shortness of breath) Aspirin: 81 mg, 1 tablet, Oral, daily Cholecalciferol: 2,000 units, Oral, daily Sertraline: 100 mg, Oral, bid
  • 6. Physical Examination in ED 8:30 PM: Vitals: TMax: 36.9; HR: 126 regular; RR: 20; SpO2: 98 % on RA BP: 128/95 mm hg. Height: 152.4 cm Weight: 76.4 kg BMI:32.89 General: Alert and oriented, no acute distress Skin: Normal for ethnicity, No edema, Not pale. HENT: Normocephalic, Oral mucosa is moist, No pharyngeal erythema. Eye: Pupils are equal, round and reactive to light, Normal conjunctiva. Neck: Supple, No carotid bruit, No jugular venous distention, No lymphadenopathy. Respiratory: No chest wall tenderness, lungs are clear to auscultation, respirations are nonlabored Cardiovascular: Regular rhythm, No murmur, Tachycardia, Good pulses equal in all extremities, No edema. Gastrointestinal: Soft, Non-tender, Normal bowel sounds. Lymphatics: No lymphadenopathy neck, axilla, groin. Musculoskeletal: Normal range of motion, Normal strength, No swelling. Integumentary: Warm, Dry, Pink. Neurologic: Alert, Oriented, No focal defects. Psychiatric: Cooperative, Appropriate mood & affect. Genitourinary: No Costovertebral Angle tenderness.
  • 7. HPI continues… After arriving on floor, Nurse notifies NP on the floor that patient had become very short of breath and wheezing
  • 8. Review of Systems on floor at 11:37 PM: Constitutional: Weakness, No fever, No chills, No fatigue, No decreased activity, No loss of appetite, No weight gain. Eye: No recent visual problem, No double vision. Ear/Nose/Mouth/Throat: No decreased hearing, No ear pain, No nasal congestion, No sore throat. Respiratory: Shortness of breath, Cough, Wheezing, No hemoptysis. Cardiovascular: Tachycardia, No palpitations, No peripheral edema. Chest pain: Midsternal, Anterior. Gastrointestinal: Nausea, Vomiting, Diarrhea, No constipation, No abdominal pain. Genitourinary: No dysuria, No change in urine stream. Hematology/Lymphatics: No swollen lymph glands. Endocrine: No excessive thirst. Immunologic: Not immunocompromised. Musculoskeletal: No neck pain, No joint pain, No decreased range of motion. Integumentary: No rash, No pruritus, No petechiae, No skin lesion. Neurologic: Alert and oriented X4, No confusion, No numbness, No tingling, No headache. Psychiatric: Anxiety, Depression.
  • 9. Physical Examination on floor at 11:27 PM: Vitals: TMax: 36.9; HR: 104 regular; RR: 32; SpO2: 94 % on 2 L/m BP: 127/94 mm hg. Height: 152.4 cm Weight: 76.4 kg BMI:32.89 General: Alert and oriented, Severe distress, not able to complete full sentences. Skin: Normal for ethnicity, No edema, Not pale. HENT: Normocephalic, Oral mucosa is moist, No pharyngeal erythema. Eye: Pupils are equal, round and reactive to light, Normal conjunctiva. Neck: Supple, No carotid bruit, No jugular venous distention, No lymphadenopathy. Respiratory: No chest wall tenderness. Respiratory rate: 30 breaths/minute, Tachypneic. Pattern: Regular. Breath sounds: Right, Upper lobe, Lower lobe, Diminished, Expiratory wheezes, No crackles present. Right lower lung dull to percussion Cardiovascular: Regular rhythm, No murmur, Tachycardia, Good pulses equal in all extremities, No edema. Gastrointestinal: Soft, Non-tender, Normal bowel sounds. Lymphatics: No lymphadenopathy neck, axilla, groin. Musculoskeletal: Normal range of motion, Normal strength, No swelling. Integumentary: Warm, Dry, Pink. Neurologic: Alert, Oriented, No focal defects. Psychiatric: Cooperative, Appropriate mood & affect. Genitourinary: No Costovertebral Angle tenderness.
  • 10. CBC 09/23 09/24 WBC 8.7 H 11.4 RBC 4.43 4.21 Hemoglobin 13.1 12.3 Hematocrit 40.4 39.2 MCV 91.2 93.1 MCH 29.6 29.2 MCHC 32.4 L 31.4 RDW 13.3 13.5 MPV 10.8 10.6 Platelets 246 223 Diff 09/23 09/24 Neutro % 0.2 0.4 Lymph % 63 91 Mono % 28 5 Eos % 8 4 Baso % 1 0 Immature Gran % 0 0 Neutro # 5.5 H 10.3 Lymph # 2.4 L 0.5 Mono # 0.7 0.5 Eos # 0.1 0.0 Baso # 0.0 0.0 Sed rate 28 General Chemistry 09/23 09/24 Sodium 140 144 Potassium 3.9 f C 2.8 Chloride 102 104 Co2 26 L 17 Anion Gap 12 H 23 BUN H 23 H 20 Creatinine H 5.8 H 5.6 Glucose 95 H 246 Calcium 8.8 8.5 Protein, Total 7.2 Albumin 4.2 Alk Phos 79 Bilirubin, Total 0.7 AST 28 ALT 25 Phosphorus eGFR L 8 L 9 eCrCl f 0.2 f 0.2 LD 416 Magnesium H 2.6 Labs:
  • 11. Blood Gases 09/24 09/24 pH 7.40 L 7.33 pCo2 37 33 pO2 L 58 87 HCO3 23 L 17 O2 Sat L 91 97 L/min 2 3 Urine Analysis UA Color Straw UA Clarity Clear UA SG 1.005 UA pH 7.0 UA LE A 1+ UA Nitrite Negative UA Protein A 2+ UA Protein (Qual) A Trace UA Glucose (Qual) Negative UA Ketones Negative UA Urobilinogen Negative UA Bilirubin A Trace UA Blood A 6-10 UA WBC <3 UA RBC A Rare UA Bacteria A Moderate Blood Culture Negative Blood Culture Negative Urine Culture Negative Influenza Negative Res. PCR Negative Nasal MRSA Negative
  • 12. Development of a moderate right pleural effusion with right basilar atelectasis and/or infiltrate.
  • 13. Overnight patient became extremely short of breath, unable to complete full sentences and was transferred to ICU in the morning following this x-ray finding
  • 14. Fluid Analysis Nucleated Cells f <50 RBC 2,000 Glucose f 497 LD f 222 Protein f <2.0 Hospital Course: Pt was started on peritoneal dialysis cycler on the night of admission and developed acute respiratory distress due to severe right pleural effusion. Patient was transferred to ICU, peritoneal dialysis was stopped and right thoracentesis was performed, with drainage of 3.2 L of fluid. Fluid analysis was consistent with 1.5% Dianeal concentration PD solution. Hydrothorax/Pleural effusion due to peritoneo-pleural leak. IV antibiotics for possible pneumonia with aztreonam and vancomycin Did receive Duonebs and steroid for one day due to concern for Asthma exacerbation CT chest next day showed infiltrate in right upper lobe - Reexpansion edema Vancomycin was discontinued and continued on aztreonam She was started on hemodialysis and discharged home on 9/28/2016
  • 15. 09/25 CT CHEST W/O CONTRAST ● Moderately large right pleural effusion. ● Trace left pleural effusion present. ● Infiltrate in the right upper lobe. ● Partial consolidation and atelectasis noted in the right middle lobe and right lower lobe. ● Left basilar infiltrate and atelectasis noted. ● 0.2 m noncalcified nodule
  • 16. “Sweet Hydrothorax” Acute Hydrothorax Complicating Peritoneal Dialysis
  • 17. PLEURAL EFFUSION DUE TO PLEUROPERITONEAL LEAK: Hydrothorax associated with abnormal communications between the pleura and peritoneal cavities was first described by Meigs, who reported the coexistence of pleural effusion and ascites associated with ovarian fibroma Typically occurs early in the course of PD Not related to the volume of instilled dialysate Source of the leak - Congenital or acquired communications between the pleura and the peritoneum Diaphragmatic hernias allow dissection of fluid through defects around the major vessels and the esophagus or through diaphragmatic foramina Negative intrathoracic pressure, combined with an increased intra-abdominal pressure caused by dialysate instillation, may open small defects in the diaphragm - promote the flow of dialysate into the pleural space. Acquired diaphragmatic defects - eight years after starting peritoneal dialysis
  • 18. Epidemiology: Incidence is 1.6 to 10 percent largest study reported to date - 50 of 3195 patients (1.6 percent) developed acute hydrothorax after starting peritoneal dialysis Women are affected more commonly than men Patients with polycystic kidney disease are predisposed to develop pleuroperitoneal leaks - Significantly reduced abdominal capacity Marked increase in hydrostatic pressure after the infusion of dialysate Peritonitis increases the incidence of hydrothorax - 6% suffered peritonitis Clinical characteristics: Dyspnea and inadequate ultrafiltration ability Asymptomatic (26 percent) Right side - 50 to 90 percent of cases Most appear early after the initiation of peritoneal dialysis 50% - within 30 days of starting PD 20% - after one year
  • 19. Diagnosis: Dyspneic nonedematous patient Ultrafiltration is consistently inadequate Modalities for the diagnosis of abdominal and thoracic cavity defects in peritoneal dialysis patients PERITONEAL SCINTIGRAPHY Safe, accurate, and rapid way of diagnosing leaks in the peritoneal cavity. 3 to 5 millicuries of technetium 99m isotope per 0.5 to 2.0 L of dialysis solution is injected into the abdominal cavity. Multiple projections (anterior, lateral, posterior, and oblique) are then taken to help diagnose leaks, hernias, and hydrothorax Although a significant dose of isotope is used, it is not absorbed from the peritoneum, and almost all of the material drains out of the body after the procedure. The net dose of radiation is therefore only a fraction of the total dose instilled into the peritoneal cavity
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  • 22. CT SCANS AND CT PERITONEOGRAPHY Accurate and reliable methods of diagnosing peritoneal defects. CTP Vs CTS - small leaks, adhesions, loculated fluid collections, intraabdominal abscesses, and pseudocysts The dose of iodinated contrast - 50 mL per liter of dialysis fluid. Oral and intravenous (IV) contrast can be simultaneously given to diagnose any abscesses or tumors CTP is not effective in diagnosing obstruction of the catheter by fibrinous, adhesions or omentum Recommend CTP as the initial diagnostic modality to be utilized. Cumulative radiation exposure may be of concern in pediatric populations. MRI AND MR PERITONEOGRAPHY Gadolinium based dye Moderate to advanced renal failure (dialysis dependent or eGFR <30 mL/min) - severe syndrome of nephrogenic systemic fibrosis.
  • 23. CLINICAL METHODS: Easy to perform, but not sensitive enough to diagnose these defects Thoracentesis Especially helpful in patients who are acutely symptomatic Diagnostic as well as therapeutic. Dialysate fluid in the pleura should have a higher concentration of glucose than plasma (50 mg/dl) Concentrations of lactate dehydrogenase (LDH) and protein are consistent with a transudate Cell count and cultures (to exclude infection) L and D isomers of lactate - L isomer of lactate is endogenous Commercial dialysis solutions have both L and D isomers Methylene blue dye — Instillation of methylene blue dye into the peritoneum - useful in diagnosing leaks. Some case reports of irritation to the abdominal viscera Clinical observation — An easier, but relatively insensitive method of diagnosing hydrothorax. keep the abdomen dry overnight and to repeat a chest radiograph in the morning to determine if the pleural effusion has decreased
  • 24. Management: Depends upon the acuity and severity of the patient's symptoms and desire to continue with peritoneal dialysis as a treatment modality Acute thoracentesis to remove large pleural effusions is rarely required Most cases - draining the peritoneal cavity and avoiding overnight (supine) dwells is sufficient If the leak is small and the patient has adequate residual function to permit intermittent dialysis (eg, nocturnal peritoneal dialysis) - PD can be continued. Continued - if estimated duration of dialysis is short, such as the patient who will soon undergo a living, related transplant Some pleuroperitoneal leaks spontaneously resolve (after temporary transfer to hemodialysis) - Cure rate is only 40 percent with conservative therapy
  • 25. Chemical pleurodesis - Recurrent pleural effusion, unresponsive to conservative measures, who needs and/or desires to continue with peritoneal dialysis In one review, pleural effusion resolved after pleurodesis in 67 percent of patients Agents - Autologous blood, talc, and tetracycline Temporary cessation of CAPD - first-line treatment Video-assisted thoracoscopic pleurodesis or repair - who failed conservative management Surgical correction of an identified diaphragmatic defect - Thoracotomy Most patients with pleuroperitoneal leaks ultimately require permanent transfer to hemodialysis
  • 26. Noninfectious complications of continuous peritoneal dialysis Continuous ambulatory peritoneal dialysis [CAPD] and Continuous cycler peritoneal dialysis [CCPD] Due to increased intra abdominal pressure resulting from instillation of dialysate into the peritoneal cavity Hernia formation Leaks (including hydrothorax or pleuroperitoneal leaks) Local edema Back pain GI problems: gastroesophageal reflux, delayed gastric emptying Not related to increased intra abdominal pressure Hemoperitoneum Pain on infusion of dialysate Electrolyte imbalances Ultrafiltration failure
  • 27. GERD - Increased intraabdominal pressure on lower esophageal sphincter Delayed gastric emptying - mechanical or neurogenic mechanism triggered by the presence of intra- abdominal fluid retards gastric emptying - metoclopramide/erythromycin Back pain - Increased mechanical stress on the lumbar spine - due to the tendency of patients to assume a more lordotic position because of increased intraabdominal pressure PAIN ON DIALYSATE INFUSION — Abdominal pain often occurs with infusion of dialysate into the peritoneal cavity even in the absence of peritonitis. Acidic pH (pH 5.2 to 5.5) of conventional lactate dialysate. Poor catheter position Dialysate temperature High glucose concentration of hypertonic dialysis solutions Rx - May be treated with intraperitoneal infusion of bicarbonate/local anesthetic - Risk of contamination and peritonitis; Slowing the rate of infusion; Catheter replacement Electrolyte abnormalities: Hypokalemia and hypermagnesemia liberalization of dietary potassium and, often, oral potassium supplementation may be needed.