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Cryonics Additions + IV Bag Stuff (#18415)
### Summary: This PR fleshes out cryonics, both inside a cryotube and outside of a cryotube, and gives a pharmacist a lot more to do during those high energy rounds as they will be required to prepare and oversee any cryonic mixes. Lots of ways you can go about doing with the biggest reward being brain regeneration that bypasses oxygenation requirements, at the cost of significant downsides if done improperly. This generally empowers pharmacists and physicians and offers non-surgical treatment alternatives, though often incurs a penalty or takes a little longer than surgical treatment, so it doesn't make surgeons redundant. This list'll be exhaustive so medical players aren't left in the dark and can just refer to this while a wiki update is worked on, instead of digging through code. **Changes to Stasis/Cryotubes:** - Stasis at temperates between 120K and 200K has been reduced to between 5 and 10, as opposed to 10 and 20. This means chemicals still have a good chance of metabolising if you set a cryotube to above ~140K. Cryotubes will still achieve good stasis if you cool below 120K - upgraded stockparts from the workshop/R&D will help with this. - (Bugfix) IPCs will not longer be knocked unconscious if they enter an active cryotube. **Misc. Reagent Additions/Tweaks:** - Bicaridine now only requires 30u in the blood to begin attempting to repair arterial bleeds, as opposed to 50u. - Adds a Blood Thinning chemical effect. This prevents Coagzolug's blood clotting effect from working and works in the opposite way - increasing how much blood you lose per blood loss tick. Fluvectionem and Synaptizine apply Blood Thinning at a strength of 25, translating to 25% faster blood loss. **Cryonic Chemicals:** - Cryoxadone and Clonexadone both overdose at 5u. **_This is not a problem when using a cryotube due to how cryotubes administer reagents._** Overdosing either results in genetic damage and severe eye damage. - Cryoxadone and Clonexadone's organ healing capabilities have been significantly nerfed. The organ healing is still noticable and useful for pharmacist/surgeonless rounds; they cannot heal the brain though. - Cryosurfactant has been renamed to Cryosilicate, mimicking Pyrosilicate - the recipe now uses silicate instead of surfactant. - Cryosilicate and Pyrosilicate now have an effect when used in the body: cryosilicate will supercool a patient; pyrosilicate will chemically incinerate someone. Leporazine will inhibit these functions. - Bicaridine will repair arterial bleeds when used in cryogenic conditions. - Kelotane will repair disfigurement when used in cryogenic conditions. - Peridaxon 2x effective in cryogenic conditions. Peridaxon can denecrotise livers and kidneys in extracool cryogenic conditions - it cannot denecrotise other organs. Using peridaxon in cryogenic conditions will result in benign tumour growth (see below). - Red Nightshade can repair bone breaks in cryogenic conditions. It will still put a patient into a berserk state. - Cataleptinol - see below. **Cataleptinol Rework:** Cataleptinol has been reworked from the ground up and is where pharmacist's will be able to shine by making fancy cryotube beaker mixers or cryonic mixtures for use in IV stands. - The new recipe is 2 parts Alkysine, 0.5 parts Phoron, 1 part Clonexadone and a 5u Cryosilicate catalyst. This translates to: 120u Alkysine + 60u Clonexadone + 30u Phoron w/ 5u Cryosilicate = 60u (1 bottle) of Cataleptinol - expensive and lots of tricky precursors, leaves enough left over to make a 2nd bottle without having to remake all of the precursors. - **In cryogenic conditions**, Cataleptinol will restore 7.5% brain activity per metabolisation tick. This _bypasses the 85% oxygenation requirement_, at the cost of hallucinations, blood thinning and liver damage. The trade is roughly 40% brain activity (assuming nothing is causing brain damage) for total liver failure. - **Outside of cryogenic conditions**, Cataleptinol becomes a lot less reliable and a lot more dangerous to use, with only a 75% chance of restoring 2% brain activity per metabolisation tick. It will still bypass oxygenation requirements, making it useful during _**severe emergencies**_, at the cost of inducing painshock in addition to the above hallucinations, blood thinning and liver damage. The trade is roughly 25% brain activity (assuming nothing is causing brain damage) for total liver failure. - Cataleptinol _**overdoses at 3u**_ and has a fast metabolisation of 0.6u/tick - this makes it hard to dose without using an IV drip. If you overdose Cataleptinol by using another method of administration, then the patient's liver will crash, brain regeneration undone and the patient will have severe seizures resulting in more pain. Using Cataleptinol outside of cryogenic conditions **is high risk and only potentially high reward**, but it could buy a couple more minutes. **Tumours:** - Adds Benign Tumours. Benign tumours simply drain nutrition and cause frequent pain; they do not spread or affect nearby organs. - Adds Malignant Tumours. Malignant tumours will begin by draining nutrition then effecting symptoms based on the tumour's location (chest tumours -> coughing, gasping, chest pain; brain tumours -> disorientation, memory loss; abdominal -> vomiting, abdominal pain; anywhere else -> lethargy). In the later stages, malignant tumours will begin to damage the organs they are close to, then will eventually enter the circulatory _~~and lymphatic~~_ system and spawn more malignant tumours in other parts of the body. - Peridaxon will result in benign tumour growth when overdosed or used in cryogenic conditions. - Genetic damage will result in malignant tumour growth. - Ryetalyn is the anti-tumour drug and will put both benign and malignant tumours into recession. You can also surgically intervene and excise tumours as you would k'ois mycosis or fluke parasites. - You cannot have more than 3 of any tumour - things won't get too out of hand. **IV Bag Stuff:** - Adds 2 labels for IV bags: Cryonics Mixture, denoted by a CR; Other Mixture, denoted by an M. - Renames `blood packs` to `IV bags` and changes their formatting. What was `blood pack O+` will now appear as `IV bag - O+ Blood`; `blood pack Saline Plus` -> `IV bag - Saline Plus`. **Misc.:** - Only 20 genetic degradation on a limb is required to deform it instead of 30. This should make it slightly more common, as 30 is a large number to reach when this number is calculated per limb. - Seizures can be given variable strengths. - (Bugfix) Coolant tanks no longer just set a room's temperature to 0K when destroyed. The amount it cools a room scales with the amount of coolant still in the tank but cannot go below 173K/-100°C. - Cryocells now have stockparts and can be upgraded/deconstructed.
This commit is contained in:
smellie
@@ -8,6 +8,7 @@
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max_damage = 45
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min_broken_damage = 25
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relative_size = 5
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toxin_type = CE_OCULOTOXIC
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var/list/eye_colour = list(0,0,0)
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var/singular_name = "eye"
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@@ -148,8 +148,10 @@
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if(temp.status & ORGAN_ARTERY_CUT)
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var/bleed_amount = FLOOR((owner.vessel.total_volume / (temp.applied_pressure || !open_wound ? 450 : 250)) * temp.arterial_bleed_severity, 1)
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if(bleed_amount)
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if(CE_BLOODCLOT in owner.chem_effects)
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if((CE_BLOODCLOT in owner.chem_effects) && !(owner.chem_effects[CE_BLOODTHIN]))
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bleed_amount *= 0.8 // won't do much, but it'll help
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if(CE_BLOODTHIN in owner.chem_effects)
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bleed_amount *= 1+(owner.chem_effects[CE_BLOODTHIN]/100)
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if(open_wound)
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blood_max += bleed_amount
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do_spray += "[temp.name]"
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@@ -1526,7 +1526,7 @@ Note that amputating the affected organ does in fact remove the infection from t
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if(genetic_degradation <= 30)
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if(status & ORGAN_MUTATED)
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unmutate()
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to_chat(src, "<span class = 'notice'>Your [name] is shaped normally again.</span>")
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to_chat(src, SPAN_NOTICE("Your [name] is shaped normally again."))
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return -(genetic_degradation - last_gene_dam)
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/obj/item/organ/external/proc/add_genetic_damage(var/amount)
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@@ -1536,10 +1536,12 @@ Note that amputating the affected organ does in fact remove the infection from t
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return
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var/last_gene_dam = genetic_degradation
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genetic_degradation = min(100,max(0,genetic_degradation + amount))
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if(genetic_degradation > 30)
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if(genetic_degradation > 10)
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owner.infest_with_parasite(owner, BP_TUMOUR_SPREADING, src)
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if(genetic_degradation > 20)
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if(!(status & ORGAN_MUTATED) && prob(genetic_degradation))
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mutate()
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to_chat(owner, "<span class = 'notice'>Something is not right with your [name]...</span>")
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to_chat(owner, SPAN_NOTICE("Something is not right with your [name]..."))
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return (genetic_degradation - last_gene_dam)
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// Pain/halloss
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@@ -73,3 +73,25 @@
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/obj/item/organ/internal/parasite/proc/stage_effect()
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return
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/mob/living/carbon/human/proc/infest_with_parasite(var/mob/living/carbon/victim, var/parasite_type, var/obj/item/organ/external/organ_to_infest, var/chance_to_infest = 100, var/parasite_limit = 3)
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if(ishuman(victim))
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var/mob/living/carbon/human/H = victim
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if(BP_IS_ROBOTIC(organ_to_infest))
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return
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var/i = 0
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for(var/obj/item/organ/internal/O in H.internal_organs) //dont want there to be a silly amount of parasites
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if(istype(O, /obj/item/organ/internal/parasite))
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i++
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if((i < parasite_limit) && prob(chance_to_infest))
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switch(parasite_type) //such a shitty way to do this but i couldnt get a better alternative to work in a sane amount of time :/
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if("malignant tumour")
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var/obj/item/organ/internal/parasite/malignant_tumour/P = new()
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P.parent_organ = organ_to_infest
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P.replaced(H, organ_to_infest)
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P.generate_name()
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if("benign tumour")
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var/obj/item/organ/internal/parasite/benign_tumour/P = new()
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P.parent_organ = organ_to_infest
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P.replaced(H, organ_to_infest)
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P.generate_name()
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@@ -0,0 +1,141 @@
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/obj/item/organ/internal/parasite/benign_tumour
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name = "benign tumour"
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icon = 'icons/obj/organs/organs.dmi'
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icon_state = "tumour"
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dead_icon = "tumour"
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organ_tag = BP_TUMOUR_NONSPREADING
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parent_organ = BP_CHEST
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subtle = 1
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drug_resistance = 1
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max_stage = 3
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stage_interval = 300 //~5 minutes minutes/stage
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origin_tech = list(TECH_BIO = 2)
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/obj/item/organ/internal/parasite/benign_tumour/proc/generate_name()
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if(parent_organ)
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switch(parent_organ)
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if(BP_CHEST)
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name = "benign chest lipoma"
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if(BP_GROIN)
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name = "benign abdominal tumour"
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if(BP_HEAD)
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name = "benign skull cavity tumour"
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if(BP_L_ARM)
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name = "benign lipoma (left arm)"
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if(BP_R_ARM)
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name = "benign lipoma (right arm)"
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if(BP_L_HAND)
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name = "benign chondroma (left hand)"
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if(BP_R_HAND)
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name = "benign chondroma (right hand)"
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if(BP_L_LEG)
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name = "benign lipoma (left leg)"
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if(BP_R_LEG)
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name = "benign lipoma (right leg)"
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if(BP_L_FOOT)
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name = "benign plantar fibroma (left foot)"
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if(BP_R_FOOT)
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name = "benign plantar fibroma (right foot)"
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/obj/item/organ/internal/parasite/benign_tumour/process()
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..()
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if (!owner)
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return
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if(REAGENT_VOLUME(owner.reagents, /singleton/reagent/ryetalyn)) //10u will treat most tumours, 20u will nuke fully developed tumours
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recession = 20
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if(prob(2))
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owner.adjustNutritionLoss(5)
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if(stage >= 2) //after ~5 minutes
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if(prob(5))
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owner.adjustHalLoss(10*stage)
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/obj/item/organ/internal/parasite/malignant_tumour
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name = "malignant tumour"
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icon = 'icons/obj/organs/organs.dmi'
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icon_state = "tumour"
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dead_icon = "tumour"
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organ_tag = BP_TUMOUR_SPREADING
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parent_organ = BP_CHEST
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subtle = 1
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drug_resistance = 1
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max_stage = 4
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stage_interval = 300 //~5 minutes minutes/stage
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origin_tech = list(TECH_BIO = 3)
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egg = /singleton/reagent/toxin/malignant_tumour_cells
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/obj/item/organ/internal/parasite/malignant_tumour/proc/generate_name()
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if(parent_organ)
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switch(parent_organ)
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if(BP_CHEST)
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name = "malignant chest wall sarcoma"
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if(BP_GROIN)
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name = "gastric cancer"
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if(BP_HEAD)
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name = "malignant brain tumour"
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if(BP_L_ARM)
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name = "malignant melanoma (left arm)"
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if(BP_R_ARM)
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name = "malignant melanoma (right arm)"
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if(BP_L_HAND)
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name = "malignant chondrosarcoma (left hand)"
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if(BP_R_HAND)
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name = "malignant chondrosarcoma (right hand)"
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if(BP_L_LEG)
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name = "malignant melanoma (left leg)"
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if(BP_R_LEG)
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name = "malignant melanoma (right leg)"
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if(BP_L_FOOT)
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name = "malignant chondrosarcoma (left foot)"
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if(BP_R_FOOT)
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name = "malignant chondrosarcoma (right foot)"
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/obj/item/organ/internal/parasite/malignant_tumour/process()
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..()
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if (!owner)
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return
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if(REAGENT_VOLUME(owner.reagents, /singleton/reagent/ryetalyn)) //10u will treat most tumours, 20u will nuke fully developed tumours
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recession = 20
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if(prob(5))
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owner.adjustNutritionLoss(5)
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if(prob(5))
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owner.adjustHalLoss((10*stage)/2)
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if(stage >= 2) //after ~5 minutes
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switch(parent_organ)
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if(BP_HEAD)
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owner.confused = min(owner.confused + (stage*2), 10)
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owner.slurring = min(owner.slurring + (stage*2), 50)
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if(prob(5))
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to_chat(owner, SPAN_WARNING(pick("You struggle to remember the last several moments.", "You smell something funny.", "You taste something funny.", "You can't figure out how to properly string words together.", "What was I just doing?")))
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owner.emote("drool")
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if(BP_CHEST)
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if(prob(3))
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to_chat(owner, SPAN_WARNING(pick("You feel a tightness in your chest.", "You feel a little lightheaded.", "You need to take larger breaths than normal.")))
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owner.emote(pick("cough", "gasp"))
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if(BP_GROIN)
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if(prob(3))
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to_chat(owner, SPAN_WARNING(pick("You feel a sharp pain in your gut.", "You feel a little bloated.")))
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owner.visible_message("<b>[owner]</b> winces slightly.")
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owner.delayed_vomit()
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else
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if(prob(stage*2))
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to_chat(owner, SPAN_WARNING("You feel very lethargic."))
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if(stage >= 3) //after ~10 minutes
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for(var/obj/item/organ/internal/O in owner.internal_organs)
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if(O.parent_organ == parent_organ)
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if(BP_IS_ROBOTIC(O))
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continue
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if(prob(stage*stage))
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O.damage = min(O.damage+stage, O.max_damage)
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if(stage >= 4) //after 15 minutes
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if(prob(3))
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owner.reagents.add_reagent(egg, 2) //malignant cells breaking off, enter circulatory/lymphatic nodes to spread
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