Hi youngerson,
Let me start off with, I am sorry you and your
family are having this situation.
Secondly... I would like to state that Google
Answers is a resource of information and should
not be used as a "second opinion". Considering
that medicine is being "practiced", the information
that is contained herein should not be considered
absolute. Qualified examination is required for an
accurate diagnosis.
Before I begin. I surely hope this postoperative
care is being performed in the hospital?
If this is in a hospital, why have they allowed
it to go on this long? Everything I have read
about her current condition seems to indicate
it is a dire situation. From what I have gathered
it appears that the surgery was not successful.
What started as an appendicitis and progressed to
a ruptured appendicitis appears to have now
become Abdominal Sepsis or Peritonitis.
What follows is alot of text from emedicine.com.
I have found that their information is very in
depth and thorough. You can jump to the bottom
for the summary of answers to your questions 1-4.
-=-=-=-=-=-=-=-=-=-=-=-
"Peritonitis and Abdominal Sepsis
Author: Thomas Genuit, MD, Assistant Professor, Department
of Surgery, Program in Trauma and Surgical Critical Care,
University of Maryland School of Medicine
Coauthor(s): Lena Napolitano, MD, Vice-Chair, Department of
Surgery, VA Maryland Healthcare System; Professor,
Department of Surgery, University of Maryland School of
Medicine
on emedicine.com
[ http://www.emedicine.com/med/topic2737.htm ]
"Peritonitis is defined as inflammation of the serosal
membrane that lines the abdominal cavity and the organs
contained therein. Peritonitis is often caused by
introduction of an infection into the otherwise sterile
peritoneal environment through perforation of the bowel,
such as a ruptured appendix."
-=-=-=-=-=-=-=-=-=-=-=-
"Peritoneal infections are classified as primary (ie,
spontaneous), secondary (ie, related to a pathologic
process in a visceral organ), or tertiary (ie, persistent
or recurrent infection after adequate initial therapy). The
intra-abdominal infection may be localized or generalized,
with or without abscess formation."
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"The spectrum of pathogens depends to some degree on the
site of the original disease. Gram-positive organisms
predominate in the upper GI tract; however, a shift toward
gram-negative organisms may be noticed in patients on
long-term gastric acid suppressive therapy. Contamination
from a distal small bowel or colon source initially may
result in the release of several hundred bacterial species
(and fungi); host defenses quickly eliminate most of these
organisms. The resulting peritonitis is almost always
polymicrobial, containing a mixture of aerobic and
anaerobic bacteria with a predominance of gram-negative
organisms."
-=-=-=-=-=-=-=-=-=-=-=-
"In general, the incidence of abscess formation after
abdominal surgery is less than 1-2%, even when the
operation is performed for an acute inflammatory process.
This incidence increases with preoperative perforation of
the hollow viscus, significant fecal contamination of the
peritoneal cavity, bowel ischemia, delayed diagnosis and
therapy of the initial peritonitis, the need for
reoperation, and in the setting of immunosuppression. In
these instances, the risk of abscess formation may be as
high as 10-30% (Reid, 1999). Overall, abscess formation is
the leading cause of persistent infection and development
of tertiary peritonitis.
"Tertiary peritonitis represents the persistence or
recurrence of peritoneal infection following apparently
adequate therapy of SBP or SP, often without the original
visceral organ pathology. Patients with tertiary
peritonitis usually present with an abscess, or phlegmon,
with or without fistulization. Tertiary peritonitis
develops more frequently in patients with significant
preexisting comorbid conditions and in patients who are
immunocompromised. Although rarely observed in
uncomplicated peritoneal infections, the incidence of
tertiary peritonitis in patients requiring ICU admission
for severe abdominal infections may be as high as 50-74%.
"Patients who develop tertiary peritonitis demonstrate
significantly longer lengths of stay in the ICU and
hospital, higher organ dysfunction scores, and higher
mortality rates (50-70%). Resistant and unusual organisms
(eg, Enterococcus, Candida, Staphylococcus, Enterobacter,
and Pseudomonas species) are found in a significant
proportion of cases of tertiary peritonitis. Most patients
with tertiary peritonitis develop complex abscesses or
poorly localized peritoneal infections that are not
amenable to percutaneous drainage. Antibiotic therapy
appears less effective compared to all other forms of
peritonitis (Nathens, 1998)."
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"Early control of the septic source is mandatory and can be
achieved by operative and nonoperative means. Nonoperative
interventional therapies include percutaneous drainage of
abscesses and percutaneous and endoscopic stent placements.
If an abscess is accessible to percutaneous drainage and
the underlying visceral organ pathology does not clearly
require an operative approach, percutaneous drainage can be
used safely and effectively as the primary treatment
modality (Levison, 1992; Hemming, 1991; Rothlin, 1998).
"Operative management addresses the need to control the
infectious source and to purge bacteria and toxins. The
type and extent of surgery depends on the underlying
disease process and the severity of intra-abdominal
infection (Wittmann, 1998). Open treatment allows for
thorough drainage of the intra-abdominal infection, but the
specific indications are not clearly defined."
-=-=-=-=-=-=-=-=-=-=-=-
"Lab Studies:
"In general, perform a complete blood cell (CBC) count with
differential in patients who present with peritoneal
infections and evaluate the serum electrolyte panel with
blood urea nitrogen (BUN) and creatinine.
"Most patients with intra-abdominal infections demonstrate
leukocytosis (>11,000 cells/mL) with a shift to the immature
forms on the differential cell count. Patients in severe
sepsis, patients who are immunocompromised, and patients with
certain types of infections (eg, fungal, cytomegaloviral) may
demonstrate absence of leukocytosis or leucopenia.
"Blood chemistry findings are often within the reference range
initially, but they may show evidence of dehydration with
elevated BUN and altered electrolyte concentrations caused by
protracted vomiting, diarrhea, fistulae, renal dysfunction,
and ascites. Some degree of metabolic acidosis may be
present.
"Obtain a coagulation profile (ie, prothrombin time [PT] and
activated partial thromboplastin time [aPTT]) if no recent
values within the reference range are available and an
operation or interventional procedure is planned.
"Perform liver function tests (ie, alanine aminotransferase,
glutamine aminotransferase, alkaline phosphatase, total and
direct bilirubin, serum protein, albumin) if hepatic
dysfunction, malnutrition, or specific hepatobiliary disease
is suspected.
"Evaluate serum amylase and lipase levels in patients with a
possible diagnosis of pancreatitis.
"Urinalysis (UA) is essential to rule out urinary tract
diseases (eg, pyelonephritis, renal colic), which may mimic
peritonitis; however, patients with lower abdominal and
pelvic infections often demonstrate WBCs in the urine and
microhematuria. The presence of frank pyuria, WBC casts,
large numbers of red blood cells, and bacteria in the
specimen suggest a urinary source of the patient's symptoms.
"In patients with diarrhea, evaluate a stool sample for
Clostridium difficile toxin assay, WBC count, and specific
culture (ie, Salmonella, Shigella, cytomegalovirus [CMV]) if
the patient's history suggests infectious enterocolitis.
"In patients with evidence of sepsis from intra-abdominal
infection, evaluate aerobic and anaerobic blood cultures for
bacteremia; however, initial culture results may be negative
in more than 90% of cases, despite clinical evidence of
sepsis (McQuaid, 1999; Eckhauser, 1997; Pai, 1995).
"Peritoneal fluid (ie, paracentesis, aspiration of abdominal
fluid collections, intraoperative peritoneal fluid cultures)
"When assessing a peritoneal fluid sample for peritoneal
infection, evaluate the sample for pH, glucose, protein,
lactate dehydrogenase (LDH), cell count, Gram stain, and
aerobic and anaerobic cultures.
"Obtain a peritoneal fluid amylase analysis if pancreatitis or
pancreatic leak is suspected. Obtain a fluid bilirubin
analysis when a biliary leak is suspected and evaluate the
fluid creatinine level when a urinary leak is suspected.
Compare the peritoneal levels to the respective serum levels.
"The fluid in bacterial peritonitis generally demonstrates low
pH and glucose as well as elevated protein and LDH levels. A
fluid pH lower than 7.1 (and partial pressure of oxygen [PO2]
<49 mm Hg) has demonstrated positive and negative predictive
values of greater than 98% in some studies (median pH of 6.75
versus 7.49 for elective surgery, with PO2 28 versus 144 mm
Hg) (Simmen, 1993). The drop in peritoneal fluid pH (and PO2)
is more pronounced in mixed infections and severe bacterial
contamination, with increased numbers of anaerobic bacteria
in these circumstances (Sawyer RG, Spengler MD, 1991).
"In SBP, a WBC count of more than 250 cells/mL (>500 in some
studies), with more than 50% polymorphonuclear leukocytes
(PMNs) is an indication to begin antibiotic therapy. Although
up to 30% of culture findings remain negative in these
patients, most of these patients are presumed to have
bacterial peritonitis; they should be treated. A
significantly decreased peritoneal fluid glucose level (<50
mg/dL), a peritoneal fluid LDH level much greater than the
serum LDH, a peritoneal fluid WBC count greater than 10,000
cells/mL, a pH lower than 7.0, high amylase levels, multiple
organisms on Gram stain, or recovery of anaerobes from the
culture raises the suspicion of SP in these patients. Some
authors recommend repeating the paracentesis in 48-72 hours
to monitor treatment success (decrease in neutrophil count to
<50% of the original value) (Hoefs, 1985).
"In TP, the fluid Gram stain and acid-fast stain results are
rarely positive, and routine culture findings are falsely
negative in as many as 80% of cases. A peritoneal fluid
protein level greater than 2.5 g/dL, LDH level greater than
90 U/mL, and predominantly mononuclear cell count of more
than 500 cells/mL should raise the suspicion of TP, but
specificity for the diagnosis is limited. Laparoscopy with
visualization of granulomas on peritoneal biopsy and specific
culture (requires 4-6 wk) may be needed for definitive
diagnosis.
"Routine intraoperative peritoneal fluid cultures in defined
acute disease entities (ie, gastric or duodenal ulcer
perforation, appendicitis, diverticulitis or perforation of
the colon caused by obstruction or ischemia) are
controversial. Several studies have found no significant
difference in patients with appendicitis, diverticulitis, and
other common etiologies for bacterial peritonitis with regard
to postoperative complication rates or overall outcomes. The
antibiotic regimen was altered only 8-10% of the time based
on operative culture data (Bilik, 1998; Mosdell, 1991;
Farber, 1997). In patients who had previous abdominal
operations or instrumentation (eg, peritoneal dialysis
catheter, percutaneous stents) and patients with prolonged
antibiotic therapy, critical illness, and/or hospitalization,
these cultures may reveal resistant or unusual organisms that
should prompt alteration of the antibiotic strategy."
-=-=-=-=-=-=-=-=-=-=-=-
"Medical therapy: The general principles guiding the
treatment of intra-abdominal infections are 4-fold: (1) to
control the infectious source, (2) to purge bacteria and
toxins, (3) to maintain organ system function, and (4) to
control the inflammatory process.
"Medical, nonoperative interventional, and operative
treatment options are complimentary, not competitive, in
the treatment of peritoneal infections. Medical support
includes (1) systemic antibiotic therapy; (2) intensive
care with hemodynamic, pulmonary, and renal replacement
support; (3) nutrition and metabolic support; and (4)
inflammatory response modulation therapy.
"Early control of the septic source is mandatory and can be
achieved by operative and nonoperative means. Nonoperative
interventional therapies include percutaneous drainage of
abscesses and percutaneous and endoscopic stent placements.
"Operative management addresses the need to control the
infectious source and to purge bacteria and toxins. The
type and extent of surgery depends on the underlying
disease process and the severity of intra-abdominal
infection (Wittmann, 1998). Close surveillance of the
patient is mandatory. If the patient does not improve after
the initial therapy (<24-72 h), a missed focus of infection
must be sought and treated aggressively (Gallinaro, 1991).
"Treatment of peritonitis and intra-abdominal sepsis always
begins with volume resuscitation, correction of potential
electrolyte and coagulation abnormalities, and empiric
broad-spectrum parenteral antibiotic coverage."
-=-=-=-=-=-=-=-=-=-=-=-
"Surgical site infection/dehiscence
"The incidence of surgical site infection increases with the
degree of contamination; therefore, surgical site infection
occurs at much higher rates after operations for peritonitis
and peritoneal abscess (ie, 5-15% compared to <5% for
elective abdominal operations for noninfectious etiologies).
Surgical site infection may be expected if the wound is
closed in the setting of gross abdominal contamination (see
Table 4). Perioperative systemic antibiotics, the use of
wound protector devices, and lavage of the wound at the end
of therapy do not reliably prevent this complication. These
wounds should be left open and be treated with wet-to-dry
dressing changes several times a day.
"Table 4. Wound Classification and Risk for Surgical Site
"With minor contamination in otherwise healthy patients,
primary wound closure can be attempted, but this mandates
close surveillance for signs of wound infection for the
following 1-2 weeks. An alternative technique is
approximation of the skin every 1-2 inches, with placement of
Telfa or gauze wicks down to the fascia in between. The wound
is dressed in a sterile fashion and left undisturbed for 2-3
days. At the time of dressing change (under sterile
conditions), the amount and character of drainage is
assessed. With minimal serous drainage, the skin between the
primary suture sites can be approximated with Steri-Strips.
With turbid drainage or frank pus, open treatment is
continued by replacing the wicks 2-4 times a day.
"Impaired wound healing
"The same factors that impair clearance of the abdominal
infection contribute to increased problems related to wound
healing (eg, malnutrition, severe sepsis, multiple organ
system dysfunction, advanced age, immunosuppression) and
should be addressed aggressively. Patients with severe
abdominal infections demonstrate higher incidences of fascial
dehiscence and incisional hernia development, requiring later
reoperation.
"Complications related to percutaneous drainage
"Percutaneous drainage procedures carry a risk of related
significant complications of less than 10% (range 5-27%)
depending on the underlying pathology and abscess location.
These complications include bleeding, injury, erosion,
transgression of small and large bowel, fistula formation,
and others. Strategies to prevent these problems include
correction of coagulation problems and determination of the
exact etiology, location, and anatomic relationships of the
abscess. Indication for percutaneous treatment of complex
abscesses and patients with a persistent enteric leak should
be reviewed critically, and operative treatment should not be
delayed with lack of adequate patient improvement."
"Persistent infection, recovery of enterococci, and
multidrug-resistant gram-negative organisms, as well as
fungal infection, are related to worse outcomes and recurrent
complications (Berger, 1998).
"Patients older than 65 years have a 3-fold increased risk of
developing generalized peritonitis and sepsis from gangrenous
or perforated appendicitis and perforated diverticulitis than
younger patients and are 3 times more likely to die from
these disease processes (Watters, 1996). Older patients with
perforated diverticulitis are 3 times more likely than
younger patients to have generalized rather than localized
(ie, pericolic, pelvic) peritonitis. These findings are
consistent with the hypothesis that the biologic features of
peritonitis differ in elderly persons, who are more likely to
present with an advanced or more severe process than younger
patients with peritonitis.
"Overall, studies suggest that host-related factors are more
significant than the type and source of infection with regard
to the prognosis in intra-abdominal infections (Pacelli, 1996)"
-=-=-=-=-=-=-=-=-=-=-=-
"FUTURE AND CONTROVERSIES
Section 9 of 11
"IOPL remains a controversial area in the operative treatment
of peritoneal infections. Individual studies report positive
effects of IOPL (see Intraoperative lavage). However,
although removal of gross contamination appears logical, the
addition of antimicrobial or antiseptic agents or
large-volume IOPL has been associated with disturbance of
peritoneal surface integrity and alteration of peritoneal
immune function. Overall, the benefits or safety of
crystalloid or antiseptic IOPL has not been established
clearly beyond any reasonable doubt, but it remains well
entrenched in modern surgical practice (Schein, 1998)."
=o-o= =o-o= =o-o= =o-o= =o-o= =o-o= =o-o= =o-o=
Your original Questions:
1). What is the Solution for this problem?
2). How long will it take to heal?
3). Do we have to conduct any additional tests?
4). What precautions has to take?
1) What I have read, suggests that in a case that is not
exacerbated by other medical conditions or age related issues,
surgery should be performed. A thorough cleansing and evacuation,
with an exploration to find the source of the fecal outflow.
If this has continued up to this point there must be a
perforation remaining. Either the appendectomy wound has not
sealed or there are other holes in the bowels. These need to be
taken care of immediately! Organ failure can result if this
continues.
2) Only after the recurring source of sepsis and fecal spillage
is fixed can the healing begin. Until then nothing will resolve.
In fact many items I have read indicate that a deteriorating
factor can occur that can result in mortality.
[ http://www.emedicine.com/med/topic2737.htm ]
"Patients who develop tertiary peritonitis demonstrate
significantly longer lengths of stay in the ICU and hospital,
higher organ dysfunction scores, and higher mortality rates
(50-70%). Resistant and unusual organisms (eg, Enterococcus,
Candida, Staphylococcus, Enterobacter, and Pseudomonas species)
are found in a significant proportion of cases of tertiary
peritonitis. Most patients with tertiary peritonitis develop
complex abscesses or poorly localized peritoneal infections that
are not amenable to percutaneous drainage. Antibiotic therapy
appears less effective compared to all other forms of peritonitis
(Nathens, 1998). "
"With minor contamination in otherwise healthy patients,
primary wound closure can be attempted, but this mandates
close surveillance for signs of wound infection for the
following 1-2 weeks. An alternative technique is
approximation of the skin every 1-2 inches, with placement of
Telfa or gauze wicks down to the fascia in between. The wound
is dressed in a sterile fashion and left undisturbed for 2-3
days. At the time of dressing change (under sterile
conditions), the amount and character of drainage is
assessed. With minimal serous drainage, the skin between the
primary suture sites can be approximated with Steri-Strips.
With turbid drainage or frank pus, open treatment is
continued by replacing the wicks 2-4 times a day. "
"Indication for percutaneous treatment of complex abscesses and
patients with a persistent enteric leak should be reviewed
critically, and operative treatment should not be delayed with
lack of adequate patient improvement."
3) Tests... Fecal matter is discharging. Only tests that
are indicated with such a strong presentation of a condition
such as that is exploration of the wound either non-invasively
(ultrasound, CT, MRI) or surgically by endoscopic survey or
in this case open abdominal surgery. The source of bowel
perforation needs to be found.
This is considering the hospital did the battery of tests
indicated for a peritoneal infection that I listed above
under Lab Studies?
4) Precautions... Well, this patient needs to be in a hospital.
The hospital should have a constant drip of some strong type
of antibiotic. She should be hydrated probably also with an IV.
Postoperative of the initial surgery she should have been
treated til resolution of the sepsis and fecal seepage. She
is at risk for secondary infections at this point. Organ
damage is a large likelihood if the area is not cleaned. This
needs to be treated seriously.
I'm sure that this might have raised others questions.
Please request any clarifications you might have
about my answers since there is a lot of medical jargon
involved.
-search techniques-
ruptured Appendix fecal
[
://www.google.com/search?num=20&hl=en&lr=&ie=UTF-8&oe=UTF-8&s
afe=off&q=ruptured+Appendix+fecal ]
"ruptured Appendix" OR appendicitis fecal OR "fecal spillage"
[
://www.google.com/search?q=%22ruptured+Appendix%22+OR+appendi
citis+fecal+OR+%22fecal+spillage%22&num=20&hl=en&lr=&ie=UTF-8&oe=
UTF-8&safe=off ]
ruptured Appendix fecal drainage
[
://www.google.com/search?num=20&hl=en&lr=&ie=UTF-8&oe=UTF-8&s
afe=off&q=ruptured+Appendix+fecal+drainage ]
fecal drainage peritonitis
[
://www.google.com/search?q=fecal+drainage+peritonitis&num=20&
hl=en&lr=&ie=UTF-8&oe=UTF-8&safe=off&start=20&sa=N ]
Searches also through [ http://www.emedicine.com/ ]
good luck,
-AI |