Difference between revisions of "Hyperthermic intraperitoneal chemotherapy surgery"
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}}'''Hyperthermic intraperitonal chemotherapy surgery (HIPEC)''' and '''cytoreductive surgery''' is a combined procedure utilized to treat peritoneal surface cancers.<ref name=":0">{{Cite journal|last=Webb|first=Christopher Allen-John|last2=Weyker|first2=Paul David|last3=Moitra|first3=Vivek K.|last4=Raker|first4=Richard K.|date=2013 | }}'''Hyperthermic intraperitonal chemotherapy surgery (HIPEC)''' and '''cytoreductive surgery''' is a combined procedure utilized to treat peritoneal surface cancers.<ref name=":0">{{Cite journal|last=Webb|first=Christopher Allen-John|last2=Weyker|first2=Paul David|last3=Moitra|first3=Vivek K.|last4=Raker|first4=Richard K.|date=2013|title=An overview of cytoreductive surgery and hyperthermic intraperitoneal chemoperfusion for the anesthesiologist|url=https://pubmed.ncbi.nlm.nih.gov/23460568|journal=Anesthesia and Analgesia|volume=116|issue=4|pages=924–931|doi=10.1213/ANE.0b013e3182860fff|issn=1526-7598|pmid=23460568|via=}}</ref> These cancers include secondary peritoneal carcinomatosis, pseudomyxoma peritonei and primary peritoneal tumors.<ref name=":0" /><ref>{{Cite journal|last=Macrì|first=Antonio|date=2010-01-15|title=New approach to peritoneal surface malignancies|url=https://pubmed.ncbi.nlm.nih.gov/21160811|journal=World Journal of Gastrointestinal Oncology|volume=2|issue=1|pages=9–11|doi=10.4251/wjgo.v2.i1.9|issn=1948-5204|pmc=2999159|pmid=21160811}}</ref> Cytoreductive surgery involves debulking the majority of tumors until the remainder are small enough to ensure adequate efficacy with HIPEC. | ||
HIPEC involves infusing heated cytotoxic chemotherapeutic drugs directly into the surgical site in order to effectively penetrate involved cancer while limiting exposure to normal tissue and decrease systemic uptake.<ref name=":0" /><ref name=":1">{{Cite journal|last=Schmidt|first=C.|last2=Moritz|first2=S.|last3=Rath|first3=S.|last4=Grossmann|first4=E.|last5=Wiesenack|first5=C.|last6=Piso|first6=P.|last7=Graf|first7=B. M.|last8=Bucher|first8=M.|date=2009-09-15|title=Perioperative management of patients with cytoreductive surgery for peritoneal carcinomatosis|url=https://pubmed.ncbi.nlm.nih.gov/19697426|journal=Journal of Surgical Oncology|volume=100|issue=4|pages=297–301|doi=10.1002/jso.21322|issn=1096-9098|pmid=19697426}}</ref><ref>{{Cite journal|last=Al-Shammaa|first=Hassan-Alaa-Hammed|last2=Li|first2=Yan|last3=Yonemura|first3=Yutaka|date=2008-02-28|title=Current status and future strategies of cytoreductive surgery plus intraperitoneal hyperthermic chemotherapy for peritoneal carcinomatosis|url=https://pubmed.ncbi.nlm.nih.gov/18300340|journal=World Journal of Gastroenterology|volume=14|issue=8|pages=1159–1166|doi=10.3748/wjg.14.1159|issn=1007-9327|pmc=2690662|pmid=18300340}}</ref> This may be performed in a closed abdomen via perfusion circuit or an open abdomen +/- cavity expanders.<ref>{{Cite journal|last=Witkamp|first=A. J.|last2=de Bree|first2=E.|last3=Van Goethem|first3=R.|last4=Zoetmulder|first4=F. A.|date=2001 | HIPEC involves infusing heated cytotoxic chemotherapeutic drugs directly into the surgical site in order to effectively penetrate involved cancer while limiting exposure to normal tissue and decrease systemic uptake.<ref name=":0" /><ref name=":1">{{Cite journal|last=Schmidt|first=C.|last2=Moritz|first2=S.|last3=Rath|first3=S.|last4=Grossmann|first4=E.|last5=Wiesenack|first5=C.|last6=Piso|first6=P.|last7=Graf|first7=B. M.|last8=Bucher|first8=M.|date=2009-09-15|title=Perioperative management of patients with cytoreductive surgery for peritoneal carcinomatosis|url=https://pubmed.ncbi.nlm.nih.gov/19697426|journal=Journal of Surgical Oncology|volume=100|issue=4|pages=297–301|doi=10.1002/jso.21322|issn=1096-9098|pmid=19697426}}</ref><ref>{{Cite journal|last=Al-Shammaa|first=Hassan-Alaa-Hammed|last2=Li|first2=Yan|last3=Yonemura|first3=Yutaka|date=2008-02-28|title=Current status and future strategies of cytoreductive surgery plus intraperitoneal hyperthermic chemotherapy for peritoneal carcinomatosis|url=https://pubmed.ncbi.nlm.nih.gov/18300340|journal=World Journal of Gastroenterology|volume=14|issue=8|pages=1159–1166|doi=10.3748/wjg.14.1159|issn=1007-9327|pmc=2690662|pmid=18300340}}</ref> This may be performed in a closed abdomen via perfusion circuit or an open abdomen +/- cavity expanders.<ref>{{Cite journal|last=Witkamp|first=A. J.|last2=de Bree|first2=E.|last3=Van Goethem|first3=R.|last4=Zoetmulder|first4=F. A.|date=2001|title=Rationale and techniques of intra-operative hyperthermic intraperitoneal chemotherapy|url=https://pubmed.ncbi.nlm.nih.gov/11908929|journal=Cancer Treatment Reviews|volume=27|issue=6|pages=365–374|doi=10.1053/ctrv.2001.0232|issn=0305-7372|pmid=11908929|via=}}</ref> An open abdomen technique may reduce increased intraabdominal pressures and prevent reuse of the cytotoxic solution. However, the closed abdomen technique reduces risk of exposure of the medications to the OR staff. | ||
Important perioperative considerations include temperature management, cardiovascular management, intra-abdominal pressures, metabolic derangements (depending on carrier solution of chemotherapeutic agent), potential toxicities (see table below), coagulopathy, fluid/renal management and pain management.<ref name=":0" /><ref name=":1" /> | Important perioperative considerations include temperature management, cardiovascular management, intra-abdominal pressures, metabolic derangements (depending on carrier solution of chemotherapeutic agent), potential toxicities (see table below), coagulopathy, fluid/renal management and pain management.<ref name=":0" /><ref name=":1" /> | ||
Intraoperatively, OR staff may be exposed to cytotoxic agents due to high concentrations of chemotherapeutic medications, long case duration, and smoke and or mechanical exposure. Pregnant or those actively planning for pregnancy, those with a history of congenital malformations or abortions should carefully consider participation in HIPEC cases. Safety precautions including high-power filtration masks, eye protection, gloves, and standard universal precautions should always be heeded.<ref>{{Cite journal|last=González-Moreno|first=Santiago|last2=González-Bayón|first2=Luis|last3=Ortega-Pérez|first3=Gloria|date=2012 | Intraoperatively, OR staff may be exposed to cytotoxic agents due to high concentrations of chemotherapeutic medications, long case duration, and smoke and or mechanical exposure. Pregnant or those actively planning for pregnancy, those with a history of congenital malformations or abortions should carefully consider participation in HIPEC cases. Safety precautions including high-power filtration masks, eye protection, gloves, and standard universal precautions should always be heeded.<ref>{{Cite journal|last=González-Moreno|first=Santiago|last2=González-Bayón|first2=Luis|last3=Ortega-Pérez|first3=Gloria|date=2012|title=Hyperthermic intraperitoneal chemotherapy: methodology and safety considerations|url=https://pubmed.ncbi.nlm.nih.gov/23021715|journal=Surgical Oncology Clinics of North America|volume=21|issue=4|pages=543–557|doi=10.1016/j.soc.2012.07.001|issn=1558-5042|pmid=23021715|via=}}</ref> | ||
== Preoperative management == | == Preoperative management == | ||
=== Cytotoxic Agents<ref name=":0" /><ref>{{Cite book|url=https://www.worldcat.org/oclc/751669717|title=Cancer chemotherapy and biotherapy : principles and practice|date=2011|publisher=Wolters Kluwer Health/Lippincott Williams & Wilkins|others=Bruce Chabner, Dan L. Longo|isbn=1605474312|edition=5th | === Cytotoxic Agents<ref name=":0" /><ref>{{Cite book|url=https://www.worldcat.org/oclc/751669717|title=Cancer chemotherapy and biotherapy : principles and practice|date=2011|publisher=Wolters Kluwer Health/Lippincott Williams & Wilkins|others=Bruce Chabner, Dan L. Longo|isbn=1605474312|edition=5th|location=Philadelphia|oclc=751669717|last=|first=|year=|pages=}}</ref> === | ||
{| class="wikitable" | {| class="wikitable" | ||
|+ | |+ | ||
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|- | |- | ||
|Gastrointestinal | |Gastrointestinal | ||
|Hypoalbuminemia associated with higher major mobidity<ref>{{Cite journal|last=Seretis|first=Charalampos|last2=Gill|first2=Jagjit|last3=Malik|first3=Adnan|last4=Elhassan|first4=Ali Mohamed|last5=Shariff|first5=Umar|last6=Youssef|first6=Haney|date=2020 | |Hypoalbuminemia associated with higher major mobidity<ref>{{Cite journal|last=Seretis|first=Charalampos|last2=Gill|first2=Jagjit|last3=Malik|first3=Adnan|last4=Elhassan|first4=Ali Mohamed|last5=Shariff|first5=Umar|last6=Youssef|first6=Haney|date=2020|title=Low Preoperative Serum Albumin Levels Are Associated With Impaired Outcome After Cytoreductive Surgery and Perioperative Intraperitoneal Chemotherapy for Peritoneal Surface Malignancies|url=https://pubmed.ncbi.nlm.nih.gov/33447310|journal=Journal of Clinical Medicine Research|volume=12|issue=12|pages=773–779|doi=10.14740/jocmr4362|issn=1918-3003|pmc=7781284|pmid=33447310|via=}}</ref> | ||
|- | |- | ||
|Hematologic | |Hematologic | ||
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* Resuscitate with lactated ringers or plasma-lyte (Avoid normal saline) | * Resuscitate with lactated ringers or plasma-lyte (Avoid normal saline) | ||
* Consider albumin administration for intravascular fluids | * Consider albumin administration for intravascular fluids | ||
* Maintain normothermia to mild hypothermia (target temp 35-36.5 | * Maintain normothermia to mild hypothermia (target temp 35-36.5 °C) | ||
* Monitor urine output and evaluate volume status. If UOP less than 0.5 mL/kg/hr - Consider vasopressin or norepinephrine to maintain MAP if patient is hypotensive but not hypovolemic | * Monitor urine output and evaluate volume status. If UOP less than 0.5 mL/kg/hr - Consider vasopressin or norepinephrine to maintain MAP if patient is hypotensive but not hypovolemic | ||
* Obtain pre-HIPEC chemistries (Na+, K+, Mg2+, Ca2+)<ref>{{Cite journal|last=Rothfield|first=Kenneth P.|last2=Crowley|first2=Kathy|date=2012 | * Obtain pre-HIPEC chemistries (Na+, K+, Mg2+, Ca2+)<ref>{{Cite journal|last=Rothfield|first=Kenneth P.|last2=Crowley|first2=Kathy|date=2012|title=Anesthesia considerations during cytoreductive surgery and hyperthermic intraperitoneal chemotherapy|url=https://pubmed.ncbi.nlm.nih.gov/23021714|journal=Surgical Oncology Clinics of North America|volume=21|issue=4|pages=533–541|doi=10.1016/j.soc.2012.07.003|issn=1558-5042|pmid=23021714|via=}}</ref> | ||
===== <u>HIPEC Phase</u> ===== | ===== <u>HIPEC Phase</u> ===== | ||
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*** Diuretics for hypervolemia | *** Diuretics for hypervolemia | ||
*** Volume resuscitate for hypovolemia; consider hypertonic saline if Na<130 | *** Volume resuscitate for hypovolemia; consider hypertonic saline if Na<130 | ||
* Check electrolytes (Na+, K+, Mg2+ | * Check electrolytes (Na+, K+, Mg2+, Ca2+) during HIPEC phase | ||
* Continue to check coagulation factors q4 hour | * Continue to check coagulation factors q4 hour | ||
* Goal intraperitoneal tissue temperature: 41-43 | * Goal intraperitoneal tissue temperature: 41-43 °C | ||
* Watch for core temperature >39.5 | * Watch for core temperature >39.5 °C | ||
** Consider passive cooling vs active cooling with ice | ** Consider passive cooling vs active cooling with ice | ||
** Consider cooling intraperitoneal fluids | ** Consider cooling intraperitoneal fluids | ||
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|Surgical time | |Surgical time | ||
| | | | ||
| | |Variable, dependent on tumor extent / | ||
extent of surgical resection | extent of surgical resection | ||
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|EBL | |EBL | ||
| | | | ||
| | |Variable, dependent on tumor extent/ | ||
extent of surgical resection | extent of surgical resection | ||
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|Potential complications | |Potential complications | ||
| | | | ||
| | |Surgical complications: | ||
* Anastomotic leakage | |||
* Bleeding | |||
* Infection | |||
Medical / chemo-related: | |||
* Myelosuppression (MMC) | |||
* Nephrotoxicity (Cisplatin) | |||
| | | | ||
|} | |} | ||
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|+ | |+ | ||
!Attribute | !Attribute | ||
!Mayo Clinic<ref>{{Cite journal|last=Webb|first=Christopher|last2=Day|first2=Ryan|last3=Velazco|first3=Cristine S.|last4=Pockaj|first4=Barbara A.|last5=Gray|first5=Richard J.|last6=Stucky|first6=Chee-Chee|last7=Young-Fadok|first7=Tonia|last8=Wasif|first8=Nabil|date=2020 | !Mayo Clinic<ref>{{Cite journal|last=Webb|first=Christopher|last2=Day|first2=Ryan|last3=Velazco|first3=Cristine S.|last4=Pockaj|first4=Barbara A.|last5=Gray|first5=Richard J.|last6=Stucky|first6=Chee-Chee|last7=Young-Fadok|first7=Tonia|last8=Wasif|first8=Nabil|date=2020|title=Implementation of an Enhanced Recovery After Surgery (ERAS) Program is Associated with Improved Outcomes in Patients Undergoing Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy|url=https://pubmed.ncbi.nlm.nih.gov/31605328|journal=Annals of Surgical Oncology|volume=27|issue=1|pages=303–312|doi=10.1245/s10434-019-07900-z|issn=1534-4681|pmid=31605328|via=}}</ref> | ||
! | ! | ||
! | ! |
Revision as of 01:47, 9 July 2021
Anesthesia type |
General |
---|---|
Airway |
ETT |
Lines and access |
Large bore PIV X2 Central venous access Nasogastric tube |
Monitors |
Standard ASA monitors Arterial Line (consider cardiac output monitoring) Central venous pressure |
Primary anesthetic considerations | |
Preoperative |
Baseline renal function Electrolyte status Anemia Prehabilitation Nutrition optimization |
Intraoperative |
Hemodynamic monitoring Active fluid resuscitation Normothermia or mild hypothermia Pre-HIPEC electrolytes HIPEC-phase electrolytes |
Postoperative |
Maintain urine output Consider ICU admission Prolonged vasoplegia Sodium thiosulfate infusion (12 hrs) |
Article quality | |
Editor rating | |
User likes | 0 |
Hyperthermic intraperitonal chemotherapy surgery (HIPEC) and cytoreductive surgery is a combined procedure utilized to treat peritoneal surface cancers.[1] These cancers include secondary peritoneal carcinomatosis, pseudomyxoma peritonei and primary peritoneal tumors.[1][2] Cytoreductive surgery involves debulking the majority of tumors until the remainder are small enough to ensure adequate efficacy with HIPEC.
HIPEC involves infusing heated cytotoxic chemotherapeutic drugs directly into the surgical site in order to effectively penetrate involved cancer while limiting exposure to normal tissue and decrease systemic uptake.[1][3][4] This may be performed in a closed abdomen via perfusion circuit or an open abdomen +/- cavity expanders.[5] An open abdomen technique may reduce increased intraabdominal pressures and prevent reuse of the cytotoxic solution. However, the closed abdomen technique reduces risk of exposure of the medications to the OR staff.
Important perioperative considerations include temperature management, cardiovascular management, intra-abdominal pressures, metabolic derangements (depending on carrier solution of chemotherapeutic agent), potential toxicities (see table below), coagulopathy, fluid/renal management and pain management.[1][3]
Intraoperatively, OR staff may be exposed to cytotoxic agents due to high concentrations of chemotherapeutic medications, long case duration, and smoke and or mechanical exposure. Pregnant or those actively planning for pregnancy, those with a history of congenital malformations or abortions should carefully consider participation in HIPEC cases. Safety precautions including high-power filtration masks, eye protection, gloves, and standard universal precautions should always be heeded.[6]
Preoperative management
Cytotoxic Agents[1][7]
Chemotherapeutic
agent |
End-organ toxicity |
---|---|
Platinum
(cisplatin/oxaliplatin) |
Nephrotoxicity (hypomagnesemia/hypocalemia)
Nausea/Vomiting Neurotoxicity (Peripheral neuropathy, seizure, ototoxcity, blindness) Myelosupression Anaphylaxis |
Mitomycin C
(MMC) |
Myelosupression
Pulmonary/interstitial pneumonitis nausea/vomiting/diarrhea cardiomyopathy hemolytic uremic syndrome |
5-Fluropyrimidines | GI ulcers
myelosuppression rashes, keratitis, ataxia, cognitive dysfunction coronary spasm biliary sclerosis |
Anthracyclines
(doxorubicin) |
Myelosuppression
GI mucositis Cardiomyopathy |
Patient evaluation
System | Considerations |
---|---|
Neurologic | Neurologic dysfunction risk based upon chemotherapy agents used |
Cardiovascular | Cardiomyopathy risk based upon chemotherapy agents used |
Respiratory | Pneumonitis based upon chemotherapy agents used |
Gastrointestinal | Hypoalbuminemia associated with higher major mobidity[8] |
Hematologic | Risk of profound anemia |
Renal | Renal dysfunction based upon chemotherapy used.
Monitor creatinine and GFR Abnormal electrolytes |
Endocrine | |
Other | Patients may need nutrition optimization prior to surgery
Patients can benefit from active prehabilitation prior to surgery |
Labs and studies
- CMP (particularly renal function and electrolytes)
- CBC (identify and correct anemia)
- Consider pre-albumin to evaluate nutrition status
Operating room setup
- Fluid warmer
- Arterial line setup
- ± Central line
- ± Cardiac output monitor (i.e. Flowtrack)
- NG tube
- Vasopressor drips
- Blood products
Patient preparation and premedication
- Preoperative nutrition consult
- Preoperative prehabilitation plan
Regional and neuraxial techniques
- Epidural or paravertebral blocks (if epidural is contraindicated)
Intraoperative management
Monitoring and access
- Multiple large-bore PIVs (for active fluid resuscitation)
- ± Rapid infusion catheter
- Arterial line
- ± Central venous catheter
Induction and airway management
- General anesthesia with ETT
Surgical Timeout Communication
Operative goals are crucial to delineate with the surgical team prior to incision. Key discussion points include:
- Patient Risk Factors
- DVT prophylaxis
- Fluid Goals
- Confirm urine output goals for cisplatin only
- Body Temperature Management plus additional monitors (esophageal, nasopharyngeal, bladder, axillary, etc)
- Type of chemotherapy agent used, including dilution solution and its implications on electrolytes
- Consideration for further renal protection therapy
- Trigger for blood transfusion
- Preoperative antibiotic choice
Positioning
- Supine
Maintenance and surgical considerations
Cytoreductive Phase
- Fluid resuscitation to maintain euvolemia: consider to utilize arterial line and cardiac output monitoring to guide fluid resuscitation and avoid over-resuscitation
- Check ABG and base deficit q1hour
- Check coagulation status q4 hours
- Resuscitate with lactated ringers or plasma-lyte (Avoid normal saline)
- Consider albumin administration for intravascular fluids
- Maintain normothermia to mild hypothermia (target temp 35-36.5 °C)
- Monitor urine output and evaluate volume status. If UOP less than 0.5 mL/kg/hr - Consider vasopressin or norepinephrine to maintain MAP if patient is hypotensive but not hypovolemic
- Obtain pre-HIPEC chemistries (Na+, K+, Mg2+, Ca2+)[9]
HIPEC Phase
- Maintain good muscle relaxation
- Intra-abdominal pressure may be elevated up to 26 mm Hg
- Maintain abdominal perfusion pressure of >60 (MAP – IAP)
- Manage ventilation to maintain normocarbia and normoxia
- Avoid hypervolemia during high volume resuscitation
- Check ABG and base deficit q30min to q1hour
- Treat hyperglycemia (>200) with insulin drip
- Treat hyponatremia
- Diuretics for hypervolemia
- Volume resuscitate for hypovolemia; consider hypertonic saline if Na<130
- Check electrolytes (Na+, K+, Mg2+, Ca2+) during HIPEC phase
- Continue to check coagulation factors q4 hour
- Goal intraperitoneal tissue temperature: 41-43 °C
- Watch for core temperature >39.5 °C
- Consider passive cooling vs active cooling with ice
- Consider cooling intraperitoneal fluids
- Cisplatin Perfusion ONLY:
- sodium thiosulfate bolus at start of chemoperfusion
- Sodium thiosulfate drip starts immediately after bolus over 12 hrs
- Crystalloid (avoid NS) to maintain urine output > 100mL/hr through the end of case and into PACU / ICU
Emergence
- After fascia is closed, check twitches and reverse paralysis
- Plan for extubation if hemodynamically stable, normothermic and normoxic
Postoperative management
Disposition
- Admit to ICU (consider discussion with ICU team and surgeon beforehand)
- UOP Goals: UOP 100 mL/hr (for Cisplatin only)
- May require pressors due to prolonged vasoplegia postoperatively
- Continue Sodium thiosulfate drip over 12 hours from start of perfusion (for cisplatin only)
Pain management
- PCEA
- IV acetaminophen
- ketoralac (if perfusion with MMC, no pre-existing kidney disease)
Potential complications
- variable
- surgical complications: anastomotic leakage, bleeding, infection;
- medical / chemo-related: myelosuppression (MMC),
- nephrotoxicity (Cisplatin)
Procedure variants
Open Abdominal
Perfusion |
Closed Abdominal
Perfusion |
Peritoneal Cavity
Expander | |
---|---|---|---|
Unique considerations | Decreased exposure and inhalation
of chemotherapeutic agents High intrabdominal pressures |
||
Position | Supine or low-lithotomy | ||
Surgical time | Variable, dependent on tumor extent /
extent of surgical resection |
||
Perfusion Time | Cisplatin: 90min
MMC: 100min |
||
EBL | Variable, dependent on tumor extent/
extent of surgical resection |
||
Postoperative disposition | ICU | ||
Pain management | PCEA, IV acetaminophen
occasionally ketoralac (if perfusion with MMC, no pre-existing kidney disease) |
||
Potential complications | Surgical complications:
Medical / chemo-related:
|
Enhanced Recovery After Surgery
Attribute | Mayo Clinic[10] | ||
---|---|---|---|
Nutrition | Protein and carbohydrate supplementation | ||
Intravenous Fluids | Goal directed (UOP of 0.5mL/kg/h) | ||
Pain Control | Multimodal pain therapy + TAP block | ||
Oral Intake | Clear liquid on POD 0. No NGT tube | ||
Drains & Tubes | Only when indicated | ||
Post-op Disposition | Step-down unit |
References
- ↑ 1.0 1.1 1.2 1.3 1.4 Webb, Christopher Allen-John; Weyker, Paul David; Moitra, Vivek K.; Raker, Richard K. (2013). "An overview of cytoreductive surgery and hyperthermic intraperitoneal chemoperfusion for the anesthesiologist". Anesthesia and Analgesia. 116 (4): 924–931. doi:10.1213/ANE.0b013e3182860fff. ISSN 1526-7598. PMID 23460568.
- ↑ Macrì, Antonio (2010-01-15). "New approach to peritoneal surface malignancies". World Journal of Gastrointestinal Oncology. 2 (1): 9–11. doi:10.4251/wjgo.v2.i1.9. ISSN 1948-5204. PMC 2999159. PMID 21160811.
- ↑ 3.0 3.1 Schmidt, C.; Moritz, S.; Rath, S.; Grossmann, E.; Wiesenack, C.; Piso, P.; Graf, B. M.; Bucher, M. (2009-09-15). "Perioperative management of patients with cytoreductive surgery for peritoneal carcinomatosis". Journal of Surgical Oncology. 100 (4): 297–301. doi:10.1002/jso.21322. ISSN 1096-9098. PMID 19697426.
- ↑ Al-Shammaa, Hassan-Alaa-Hammed; Li, Yan; Yonemura, Yutaka (2008-02-28). "Current status and future strategies of cytoreductive surgery plus intraperitoneal hyperthermic chemotherapy for peritoneal carcinomatosis". World Journal of Gastroenterology. 14 (8): 1159–1166. doi:10.3748/wjg.14.1159. ISSN 1007-9327. PMC 2690662. PMID 18300340.
- ↑ Witkamp, A. J.; de Bree, E.; Van Goethem, R.; Zoetmulder, F. A. (2001). "Rationale and techniques of intra-operative hyperthermic intraperitoneal chemotherapy". Cancer Treatment Reviews. 27 (6): 365–374. doi:10.1053/ctrv.2001.0232. ISSN 0305-7372. PMID 11908929.
- ↑ González-Moreno, Santiago; González-Bayón, Luis; Ortega-Pérez, Gloria (2012). "Hyperthermic intraperitoneal chemotherapy: methodology and safety considerations". Surgical Oncology Clinics of North America. 21 (4): 543–557. doi:10.1016/j.soc.2012.07.001. ISSN 1558-5042. PMID 23021715.
- ↑ Cancer chemotherapy and biotherapy : principles and practice. Bruce Chabner, Dan L. Longo (5th ed.). Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. 2011. ISBN 1605474312. OCLC 751669717.CS1 maint: others (link)
- ↑ Seretis, Charalampos; Gill, Jagjit; Malik, Adnan; Elhassan, Ali Mohamed; Shariff, Umar; Youssef, Haney (2020). "Low Preoperative Serum Albumin Levels Are Associated With Impaired Outcome After Cytoreductive Surgery and Perioperative Intraperitoneal Chemotherapy for Peritoneal Surface Malignancies". Journal of Clinical Medicine Research. 12 (12): 773–779. doi:10.14740/jocmr4362. ISSN 1918-3003. PMC 7781284. PMID 33447310.
- ↑ Rothfield, Kenneth P.; Crowley, Kathy (2012). "Anesthesia considerations during cytoreductive surgery and hyperthermic intraperitoneal chemotherapy". Surgical Oncology Clinics of North America. 21 (4): 533–541. doi:10.1016/j.soc.2012.07.003. ISSN 1558-5042. PMID 23021714.
- ↑ Webb, Christopher; Day, Ryan; Velazco, Cristine S.; Pockaj, Barbara A.; Gray, Richard J.; Stucky, Chee-Chee; Young-Fadok, Tonia; Wasif, Nabil (2020). "Implementation of an Enhanced Recovery After Surgery (ERAS) Program is Associated with Improved Outcomes in Patients Undergoing Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy". Annals of Surgical Oncology. 27 (1): 303–312. doi:10.1245/s10434-019-07900-z. ISSN 1534-4681. PMID 31605328.